JPS64240B2 - - Google Patents
Info
- Publication number
- JPS64240B2 JPS64240B2 JP56051401A JP5140181A JPS64240B2 JP S64240 B2 JPS64240 B2 JP S64240B2 JP 56051401 A JP56051401 A JP 56051401A JP 5140181 A JP5140181 A JP 5140181A JP S64240 B2 JPS64240 B2 JP S64240B2
- Authority
- JP
- Japan
- Prior art keywords
- ink
- aqueous
- oil
- liquid
- drying
- 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.)
- Expired
Links
- 239000007788 liquid Substances 0.000 claims description 36
- 239000003446 ligand Substances 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 18
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 18
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 17
- 239000000194 fatty acid Substances 0.000 claims description 17
- 229930195729 fatty acid Natural products 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- 150000004665 fatty acids Chemical class 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 14
- 238000000576 coating method Methods 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 239000012736 aqueous medium Substances 0.000 claims description 7
- 239000000976 ink Substances 0.000 description 34
- 238000001035 drying Methods 0.000 description 26
- 238000007639 printing Methods 0.000 description 21
- 239000003921 oil Substances 0.000 description 15
- 235000019198 oils Nutrition 0.000 description 15
- 239000000123 paper Substances 0.000 description 11
- 238000006116 polymerization reaction Methods 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 230000001590 oxidative effect Effects 0.000 description 9
- 239000003981 vehicle Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- -1 fatty acid ester Chemical class 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 239000002966 varnish Substances 0.000 description 4
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229920006243 acrylic copolymer Polymers 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N benzopyrazine Natural products N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000007644 letterpress printing Methods 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- LFSXCDWNBUNEEM-UHFFFAOYSA-N phthalazine Chemical compound C1=NN=CC2=CC=CC=C21 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000002383 tung oil Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- GZXXANJCCWGCSV-UHFFFAOYSA-N 2,3-Diethylpyrazine Chemical compound CCC1=NC=CN=C1CC GZXXANJCCWGCSV-UHFFFAOYSA-N 0.000 description 1
- OXQOBQJCDNLAPO-UHFFFAOYSA-N 2,3-Dimethylpyrazine Chemical compound CC1=NC=CN=C1C OXQOBQJCDNLAPO-UHFFFAOYSA-N 0.000 description 1
- JFJNVIPVOCESGZ-UHFFFAOYSA-N 2,3-dipyridin-2-ylpyridine Chemical compound N1=CC=CC=C1C1=CC=CN=C1C1=CC=CC=N1 JFJNVIPVOCESGZ-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- VEUMANXWQDHAJV-UHFFFAOYSA-N 2-[2-[(2-hydroxyphenyl)methylideneamino]ethyliminomethyl]phenol Chemical compound OC1=CC=CC=C1C=NCCN=CC1=CC=CC=C1O VEUMANXWQDHAJV-UHFFFAOYSA-N 0.000 description 1
- FHRAKXJVEOBCBQ-UHFFFAOYSA-L 2-ethylhexanoate;manganese(2+) Chemical compound [Mn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O FHRAKXJVEOBCBQ-UHFFFAOYSA-L 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- WPTCSQBWLUUYDV-UHFFFAOYSA-N 2-quinolin-2-ylquinoline Chemical compound C1=CC=CC2=NC(C3=NC4=CC=CC=C4C=C3)=CC=C21 WPTCSQBWLUUYDV-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- VFISBMJRYFYJIF-UHFFFAOYSA-N 5-methoxy-4-oxo-1h-1,10-phenanthroline-3-carboxylic acid Chemical compound N1C=C(C(O)=O)C(=O)C2=C1C1=NC=CC=C1C=C2OC VFISBMJRYFYJIF-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- UJKPHYRXOLRVJJ-MLSVHJFASA-N CC(O)C1=C(C)/C2=C/C3=N/C(=C\C4=C(CCC(O)=O)C(C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C)=C4C(C)O)/C(CCC(O)=O)=C3C Chemical compound CC(O)C1=C(C)/C2=C/C3=N/C(=C\C4=C(CCC(O)=O)C(C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C)=C4C(C)O)/C(CCC(O)=O)=C3C UJKPHYRXOLRVJJ-MLSVHJFASA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- QAEKNCDIHIGLFI-UHFFFAOYSA-L cobalt(2+);2-ethylhexanoate Chemical compound [Co+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O QAEKNCDIHIGLFI-UHFFFAOYSA-L 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- VAROLYSFQDGFMV-UHFFFAOYSA-K di(octanoyloxy)alumanyl octanoate Chemical compound [Al+3].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O VAROLYSFQDGFMV-UHFFFAOYSA-K 0.000 description 1
- HTFFABIIOAKIBH-UHFFFAOYSA-N diazinane Chemical compound C1CCNNC1 HTFFABIIOAKIBH-UHFFFAOYSA-N 0.000 description 1
- JGUQDUKBUKFFRO-CIIODKQPSA-N dimethylglyoxime Chemical compound O/N=C(/C)\C(\C)=N\O JGUQDUKBUKFFRO-CIIODKQPSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229960003569 hematoporphyrin Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 235000010187 litholrubine BK Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 description 1
- 229920006391 phthalonitrile polymer Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- ORIHZIZPTZTNCU-YVMONPNESA-N salicylaldoxime Chemical compound O\N=C/C1=CC=CC=C1O ORIHZIZPTZTNCU-YVMONPNESA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- 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
- B41M7/0027—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using protective coatings or layers by lamination or by fusion of the coatings or layers
Landscapes
- Printing Methods (AREA)
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】
本発明は、油性インキの乾燥を促進し、裏移り
を防止するために湿潤状態にあるインキ塗膜上に
塗布すべき水性オーバーコーテイング液組成物に
関する。一般に、紙、プラスチツクフイルム、木
材あるいは金属層の表面に印刷や塗装によつて着
色や絵付けを施す場合、印刷ないし塗装層の乾燥
促進あるいは塗装被膜の表面物性の向上を目的と
して塗装ないし印刷面に上塗り(オーバーコー
ト)を行うことが行われている。この場合、通
常、表面層を形成するコーテイング液(一般には
着色剤を含まない樹脂溶液)としては、有機溶剤
に樹脂を溶解させたものと、水または水とアルコ
ールの混合液中に樹脂を溶解させたものの二つに
大別することができ、後者を一般に「水性オーバ
ーコーテイング液」と呼んでいる。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an aqueous overcoating liquid composition to be applied onto a wet ink coating to accelerate the drying of oil-based inks and prevent set-off. Generally, when coloring or painting is applied to the surface of paper, plastic film, wood, or metal layers by printing or painting, the purpose of applying coloring or painting to the surface of paper, plastic film, wood, or metal layers is to accelerate the drying of the printed or painted layer or to improve the surface properties of the painted film. It is common practice to apply an overcoat to the surface. In this case, the coating liquid that forms the surface layer (generally a resin solution that does not contain a colorant) is usually one in which the resin is dissolved in an organic solvent, or one in which the resin is dissolved in water or a mixture of water and alcohol. The latter can be roughly divided into two types, and the latter is generally called ``aqueous overcoating liquid''.
平版印刷、活版印刷、製袋印刷等に用いられる
油性印刷インキは、一般に乾性油、樹脂、鉱物油
等をビヒクルとして含む。そして、このような油
性印刷インキの乾燥は、鉱物油および乾性油の一
部が紙中に浸透して紙上にやゝ粘稠な被膜が残る
状態となり(セツト)、次いで乾性油中の不飽和
脂肪酸エステルが空気中の酸素を吸収して酸化な
らびに重合反応を起して硬化することにより進行
する。このようなインキの酸化重合による乾燥
は、インキ中に含ませた脂肪酸の金属塩を触媒と
して進行する。しかしながら、このような油性印
刷インキは乾燥時間が長くかかるのが難点であ
り、特に枚葉印刷で印刷紙を棒積みした場合に
は、空気の流通が遮断されるため乾燥に更に時間
を要し、裏移り、ブロツキング等のはなはだ好ま
しくない現象の原因となつている。このため、通
常の枚葉印刷においては、不経済なスノコ取り
や、印刷機の排紙部でスプレーパウダー(スター
チ)を散布する方法がとられている。しかし、ス
プレーパウダーの散布を行う方法では、作業環境
が悪化し、又、印刷面の平滑性が失われるという
欠点がある。これに対し、近年、スプレーパウダ
ーを散布せずに、完全棒積みを行う目的で、イン
キの湿潤塗膜上に水性オーバーコーテイング液を
塗布し、裏移りを防止する試みがなされている。
しかしながらこの方法では、裏移りを減少させる
効果は得られるものの、水性オーバーコーテイン
グ液に覆われた下刷りの湿潤インキ塗膜は、より
一層酸素供給が断たれ、乾燥時間は水性オーバー
コーテイング液を施さない場合と比べ遅くなるこ
とはあつても早くはならない。 Oil-based printing inks used for planographic printing, letterpress printing, bag making printing, etc. generally contain drying oil, resin, mineral oil, etc. as a vehicle. When such oil-based printing ink dries, part of the mineral oil and drying oil penetrates into the paper, leaving a slightly viscous film on the paper (set), and then unsaturation in the drying oil The process progresses as the fatty acid ester absorbs oxygen from the air and undergoes oxidation and polymerization reactions to harden. Such drying of the ink by oxidative polymerization proceeds using a metal salt of a fatty acid contained in the ink as a catalyst. However, the disadvantage of this kind of oil-based printing ink is that it takes a long time to dry, and especially when printing paper is piled up in stacks for sheet-fed printing, it takes even longer to dry because air circulation is blocked. This causes extremely undesirable phenomena such as set-off, blocking, etc. For this reason, in normal sheet-fed printing, methods such as uneconomical slatting or dispersing spray powder (starch) at the paper discharge section of the printing machine are used. However, the method of dispersing spray powder has disadvantages in that the working environment deteriorates and the smoothness of the printed surface is lost. On the other hand, in recent years, attempts have been made to prevent set-off by applying an aqueous overcoating liquid on a wet ink coating for the purpose of complete stacking without dispersing spray powder.
However, although this method has the effect of reducing set-off, the wet ink film of the underprint covered with the aqueous overcoating liquid is further cut off from oxygen supply, and the drying time is longer than that when the aqueous overcoating liquid is applied. It may be slower than it would be without it, but it won't be faster.
本発明は、印刷面の粗面化を招かず且つインキ
塗膜の乾燥促進を通じて後加工、例えば断裁迄の
時間を短縮することを目的とする。 An object of the present invention is to shorten the time required for post-processing, for example, cutting, by promoting drying of the ink film without causing roughening of the printed surface.
本発明者らは、上述の目的で鋭意研究の結果、
脂肪酸金属塩を含む油性インキの酸化重合による
乾燥を促進する効果のある多座配位子化合物を含
む水性オーバーコーテイング液組成物を提供し、
これをインキの湿潤塗膜上に塗布することが極め
て効果的であることを見出した。 As a result of intensive research for the above-mentioned purpose, the present inventors found that
Provided is an aqueous overcoating liquid composition containing a polydentate ligand compound having the effect of promoting drying by oxidative polymerization of an oil-based ink containing a fatty acid metal salt,
We have found that applying this onto a wet coating of ink is highly effective.
本発明のオーバーコーテイング液組成物は、上
述の知見に基づくものであり、より詳しくは、脂
肪酸の金属塩を含む油性インキの湿潤塗膜上に塗
布するための水性オーバーコーテイング液組成物
であつて、水または水とアルコールとの混合物を
主要成分として含有してなる水性媒体中に、前記
脂肪酸の金属塩と反応して錯体を形成し得る多座
配位子化合物を分散させてなることを特徴とする
ものである。 The overcoating liquid composition of the present invention is based on the above-mentioned findings, and more specifically, it is an aqueous overcoating liquid composition for coating on a wet coating film of an oil-based ink containing a metal salt of a fatty acid. , characterized in that a polydentate ligand compound capable of reacting with the metal salt of the fatty acid to form a complex is dispersed in an aqueous medium containing water or a mixture of water and alcohol as a main component. That is.
上記した多座配位子化合物が、酸化重合反応に
対して脂肪酸の金属塩単独よりは有効な触媒系を
形成すること自体は既知のことである。したがつ
て、これを脂肪酸の金属塩とともに油性インキ中
に添加しておくことも考えられるところである。
しかしながら、本発明においてこのような手段を
とらずに水性オーバーコーテイング液中に多座配
位子化合物を含ませたのは、多座配位子化合物と
金属の脂肪酸塩をインキ中に含ませると以下の不
都合が認められるからである。 It is known that the above-mentioned polydentate ligand compounds form a more effective catalyst system for oxidative polymerization reactions than the metal salts of fatty acids alone. Therefore, it is conceivable to add this to the oil-based ink together with a metal salt of a fatty acid.
However, in the present invention, the reason why the polydentate ligand compound is included in the aqueous overcoating liquid without taking such measures is that when the polydentate ligand compound and the fatty acid salt of the metal are included in the ink. This is because the following inconveniences are recognized.
(イ) 黄色系のインキなどある種のインキにおいて
は長期の保存において変色が起る。(b) Some types of ink, such as yellow ink, undergo discoloration during long-term storage.
(ロ) 用途によつては酸化重合による乾燥をそれ程
に促進する必要もない場合もあるのに一律に多
座配位子化合物を配合しておくのは、不経済で
ある。(b) Depending on the application, it may not be necessary to accelerate drying by oxidative polymerization to that extent, but it is uneconomical to uniformly include a polydentate ligand compound.
(ハ) 添加量がインキに対し0.01%程度と極めて微
量のため極めて正確な計量を必要とし、インキ
の調合が困難となる。(c) Since the amount added is extremely small, about 0.01% of the ink, extremely accurate measurement is required, making it difficult to mix the ink.
また水性オーバーコーテイング液中に多座配
位子化合物を含めておき、インキの湿潤塗膜上
に塗布する方法には、次のような付加的な効果
がある。 Additionally, the method of including a polydentate ligand compound in an aqueous overcoating solution and applying it onto a wet coating of ink has the following additional effects.
(ニ) 多座配位子化合物の分散媒体が水性の方が乾
燥促進に対してより効果的である。(d) An aqueous dispersion medium for the polydentate ligand compound is more effective in accelerating drying.
(ホ) インキ塗膜の厚みムラによる乾燥速度の差を
緩和することができる。(e) Differences in drying speed due to uneven thickness of the ink coating can be alleviated.
以下、本発明をより詳細に説明する。以下の記
載において「%」および「部」はいずれも重量基
準とする。 The present invention will be explained in more detail below. In the following description, both "%" and "part" are based on weight.
本発明で用いる多座配位子化合物としては、た
とえば、ヘキサヒドロジアジン、1,2―ジアジ
ン、1,3―ジアジン、1,4―ジアジン、フタ
ラジン、ビピリジン、2,2′―ジメチルビピリジ
ン、2,2′―ジエチルビピリジン、5,5′―メチ
ル―2,2′―ビピリジン、2,3―ジメチル―
1,4―ジアジン、2,3―ジエチル―1,4―
ジアジン、ターピリジン、2,2″―ジメチルター
ピリジン、オルソフエナントロリン、オルソフエ
ナントロリン塩酸塩、3―カルボキシ―4―ヒド
ロキシ―5―メトキシ―1,10―フエナントロリ
ン、トリアジン、2,2′―ビキノリン、2―オキ
シアゾベンゼン、サリチルアルデヒド、8―オキ
シキノリン、フタロニトリル、1,3―ジフエニ
ルグアニジン、ジメチルグリオキシム、サリチル
アルドキシム、ジチオジオギザミド、トリエチレ
ンテトラミン、N,N′,N″,N―テトラサリ
チリデンテトラアミノメチルエタン、N,N′―
ビス(サリチリデン)エチレンジアミン、クロロ
フイル、ヘマトポルフイリン等が挙げられる。 Examples of the polydentate ligand compound used in the present invention include hexahydrodiazine, 1,2-diazine, 1,3-diazine, 1,4-diazine, phthalazine, bipyridine, 2,2'-dimethylbipyridine, 2,2'-diethylbipyridine, 5,5'-methyl-2,2'-bipyridine, 2,3-dimethyl-
1,4-diazine, 2,3-diethyl-1,4-
Diazine, terpyridine, 2,2″-dimethylterpyridine, orthophenanthroline, orthophenanthroline hydrochloride, 3-carboxy-4-hydroxy-5-methoxy-1,10-phenanthroline, triazine, 2,2 '-Biquinoline, 2-oxyazobenzene, salicylaldehyde, 8-oxyquinoline, phthalonitrile, 1,3-diphenylguanidine, dimethylglyoxime, salicylaldoxime, dithiodiogizamide, triethylenetetramine, N,N', N″,N-tetrasalicylidenetetraaminomethylethane, N,N′-
Examples include bis(salicylidene)ethylenediamine, chlorophyll, hematoporphyrin, and the like.
これら多座配位子化合物は、水性媒体中に分散
されるが、より好ましくは溶液状態で分散され
る。本発明において、水性媒体とは、水または水
とアルコールとの混合物を主要成分として含んで
なるものを意味する。後述するように、この水性
媒体中には、水ないしアルコールの他に、固着性
や粘着性などを調整するために、ポリビニルアル
コール、メチルセルロース、ヒドロキシプロピル
セルロース、カゼイン、ゼラチン、デキストリ
ン、水溶性アクリル樹脂、アクリロニトリル樹
脂、スチレン化アクリル共重合樹脂などを溶解な
いし懸濁分散させることもできる。上述した多座
配位子化合物を、たとえば、水に対して1〜5倍
量程度のメタノール、エタノール、イソプロピル
アルコール、ブタノール、メチルセロソルブ等の
アルコール類を混合させた水性媒体に溶解させる
ことによつて、水性オーバーコーテイング液を調
製することができる。多座配位子化合物は、オー
バーコーテイング液中に0.1〜5%の割合で含ま
せることが望ましい。0.1%未満では効果が乏し
く、5%を超えて使用すると却つて、乾燥抑制剤
として作用することがある。また水性オーバーコ
ーテイング液中には、その塗布適性を改良するた
めに、3〜20%程度の水溶性樹脂を加えることが
でき、その他、塗膜強度を与えるワツクス、乳化
安定の為の界面活性剤、耐熱性改良剤、消泡剤、
などの成分を必要に応じて加えることもできる。 These polydentate ligand compounds are dispersed in an aqueous medium, more preferably in solution. In the present invention, the aqueous medium means one containing water or a mixture of water and alcohol as a main component. As will be described later, in addition to water or alcohol, this aqueous medium contains polyvinyl alcohol, methyl cellulose, hydroxypropyl cellulose, casein, gelatin, dextrin, and water-soluble acrylic resin in order to adjust adhesion and stickiness. , acrylonitrile resin, styrenated acrylic copolymer resin, etc. can also be dissolved or suspended and dispersed. For example, by dissolving the above-mentioned polydentate ligand compound in an aqueous medium containing an alcohol such as methanol, ethanol, isopropyl alcohol, butanol, methyl cellosolve in an amount of about 1 to 5 times the amount of water. Then, an aqueous overcoating solution can be prepared. The polydentate ligand compound is desirably contained in the overcoating liquid in a proportion of 0.1 to 5%. If it is less than 0.1%, the effect is poor, and if it is more than 5%, it may act as a drying inhibitor. In addition, approximately 3 to 20% of a water-soluble resin can be added to the aqueous overcoating solution to improve its coating suitability, as well as wax to provide coating strength and surfactants to stabilize the emulsion. , heat resistance improver, antifoaming agent,
Other ingredients can also be added as needed.
本発明の水性オーバーコーテイング液を用い
て、乾燥を促進すべき油性インキは、脂肪酸の金
属塩を含むことを除き、通常のそれと特に異るも
のではない。すなわち、硬化成分としての乾性油
あるいは乾性油変性物に、更に樹脂、鉱物油、溶
剤、可塑剤、界面活性剤、繊維素、およびゴム誘
導体等を必要に応じて添加したビヒクル中に所望
の色調の有機ないし無機顔料、更には必要に応じ
て色濃度調整剤、界面活性剤等の助剤を添加して
なるものであるが、ここでは上記したビヒクルの
みをオーバープリントワニスとして用いる場合も
印刷インキに含めるものとする。何故ならば本発
明法はオーバープリントワニスに対しても、乾燥
促進効果が得られるからである。 The oil-based ink whose drying is to be promoted using the aqueous overcoating liquid of the present invention is not particularly different from ordinary ink except that it contains a metal salt of a fatty acid. That is, a desired color tone is prepared in a vehicle in which resins, mineral oils, solvents, plasticizers, surfactants, cellulose, rubber derivatives, etc. are added as necessary to a drying oil or a modified drying oil as a curing component. It is made by adding organic or inorganic pigments, and further auxiliary agents such as color density adjusting agents and surfactants as necessary.Here, even when using only the above-mentioned vehicle as an overprint varnish, printing ink shall be included in the This is because the method of the present invention can also provide a drying accelerating effect on overprint varnishes.
油性印刷インキとしては脂肪酸の金属塩を含む
ものを用いる。その例としては、コバルト、マン
ガン、鉄、カルシウム、バナジウム、セリウム、
銅、亜鉛、ジルコニウム等の金属のナフテン酸、
2―エチルヘキサン酸、オレイン酸、亜麻仁油脂
肪酸、桐油脂肪酸、トール油酸等の飽和または不
飽和の脂肪酸の塩が挙げられるがこれ以外にも前
記した多座配位子との有効な錯体を形成し酸化重
合反応を促進するものであれば任意のものが用い
られる。これらの添加量は通常の場合と特に異る
ものではない。なお、インキ中の上記脂肪酸の金
属塩は水性媒体の作用によりその構成金属が解離
し、この解離した金属イオンと前記多座配位子と
の間で錯体が形成されるものと推定される。 As the oil-based printing ink, one containing metal salts of fatty acids is used. Examples include cobalt, manganese, iron, calcium, vanadium, cerium,
Naphthenic acid of metals such as copper, zinc, zirconium, etc.
Examples include salts of saturated or unsaturated fatty acids such as 2-ethylhexanoic acid, oleic acid, linseed oil fatty acid, tung oil fatty acid, and tall oil acid. Any material can be used as long as it forms and promotes the oxidative polymerization reaction. The amount of these additions is not particularly different from the usual case. It is assumed that the constituent metals of the metal salt of the fatty acid in the ink are dissociated by the action of the aqueous medium, and a complex is formed between the dissociated metal ion and the polydentate ligand.
上記したような脂肪酸の金属塩を含む油性印刷
インキをオフセツト枚葉印刷、オフセツト輪転印
刷、活版印刷等、常法に従つて印刷した後、印刷
面に、本発明の水性オーバーコーテイング液を刷
毛塗りあるいはローラーコーテイング、または、
噴霧等により塗布して印刷インキに接触させ、印
刷インキ中の脂肪酸金属塩との協働によりインキ
の硬化乾燥を促進させる。 After printing with an oil-based printing ink containing a metal salt of a fatty acid as described above according to a conventional method such as offset sheet-fed printing, offset rotary printing, letterpress printing, etc., the aqueous overcoating liquid of the present invention is applied to the printed surface with a brush. Or roller coating, or
It is applied by spraying or the like and brought into contact with printing ink, and promotes curing and drying of the ink through cooperation with fatty acid metal salts in the printing ink.
水性オーバーコーテイング液の塗布量は、乾燥
速度との関係で合目的的に決定されるが、多座配
位子化合物量として通常0.005〜0.5g/m2、好ま
しくは0.01〜0.05g/m2の範囲の割合で塗布され
る。 The amount of the aqueous overcoating liquid to be applied is determined in relation to the drying speed, but the amount of polydentate ligand compound is usually 0.005 to 0.5 g/m 2 , preferably 0.01 to 0.05 g/m 2 It is applied at a rate in the range of .
このようにして、水性オーバーコーテイング液
を塗布した印刷インキの塗膜は、硬化が促進され
て強化され断裁時のコスレ汚れ等が著しく改善さ
れる。 In this way, the coating film of the printing ink coated with the aqueous overcoating liquid is accelerated in curing and strengthened, and wrinkles and stains during cutting are significantly improved.
従来の水性オーバーコーテイング液の塗布では
棒積みによつて裏移り、ブロツキング等の問題は
発生しないが、酸化重合反応を助長する効果はな
い。従つて印刷後の用紙断裁迄には4―10時間を
必要とするが、本発明の水性オーバーコーテイン
グ液を使用すると1―2時間で全く断裁時のコス
レの問題がなくなる。 The application of conventional aqueous overcoating liquids does not cause problems such as set-off and blocking due to stacking, but does not have the effect of promoting oxidative polymerization reactions. Therefore, it takes 4 to 10 hours to cut the paper after printing, but when the aqueous overcoating liquid of the present invention is used, the problem of curling during cutting is completely eliminated in 1 to 2 hours.
以下、実施例により更に具体的に本発明を説明
する。 Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例 1
下記配合にて酸化重合型インキ用ビヒクルを作
成した。Example 1 An oxidative polymerization type ink vehicle was prepared using the following formulation.
(1) ロジン変性フエノール樹脂(荒川化学製 タ
マノール340) 38部
(2) アマニ油 19〃
(3) 桐油 10〃
(4) 540ソルベント(日本石油社製)* 33〃
100〃
* 80パーセントパラフイン系炭化水素
540〓石油溜分
ビヒクルは成分(1)〜(3)を配合し240℃に昇温し
30分保ち、ついで成分(4)を加え、加熱源を切り放
冷して製造した。(1) Rosin-modified phenolic resin (Tamanol 340 manufactured by Arakawa Chemical) 38 parts (2) Linseed oil 19〃 (3) Tung oil 10〃 (4) 540 solvent (manufactured by Nippon Oil Co., Ltd.) * 33〃 100〃 * 80% paraffin type Hydrocarbon 540〓Petroleum distillate Vehicle is prepared by blending components (1) to (3) and heating to 240℃.
The mixture was kept for 30 minutes, then component (4) was added, the heating source was turned off, and the mixture was left to cool.
この様にして得たビヒクルにオクチル酸アルミ
ニウムをビヒクル100部に対し1.5部加え、均一混
合した後140℃迄昇温し、この温度で15分間保ち
ゲル化を行つた。この様にして作成したゲルワニ
スを用い下記配合にて酸化重合型インキを作成し
た。 To the thus obtained vehicle, 1.5 parts of aluminum octylate was added to 100 parts of the vehicle, and after uniform mixing, the temperature was raised to 140°C and kept at this temperature for 15 minutes to effect gelation. Using the gel varnish thus prepared, an oxidative polymerization type ink was prepared using the following formulation.
ゲルワニス 80.0部
カーミン6B#1(大日精化製、水溶性アゾ顔
料) 18.0〃
ポリエチレンワツクス 1.85〃
2―エチルヘキサン酸マンガン 0.1〃
2―エチルヘキサン酸コバルト 0.05〃
100.00〃
これとは別に下記配合にて水性オーバーコーテ
イング液(A液)を作成した。 Gel varnish 80.0 parts Carmine 6B#1 (manufactured by Dainichiseika, water-soluble azo pigment) 18.0〃 Polyethylene wax 1.85〃 Manganese 2-ethylhexanoate 0.1〃 Cobalt 2-ethylhexanoate 0.05〃 100.00〃 Separately, the following formulation An aqueous overcoating liquid (liquid A) was prepared.
ジヨンクリル74F(ジヨンソン社製、スチレン化
アクリル共重合樹脂45%の水懸濁液) 70部
ジヨンクリル61(ジヨンソン社製、スチレン化ア
クリル共重合樹脂25%の水懸濁液) 30〃
100〃
更に下記配合にて多座配位子化合物溶液を作成
した。Jyonkryl 74F (manufactured by Jyonson, a 45% aqueous suspension of styrenated acrylic copolymer resin) 70 parts Jyoncryl 61 (manufactured by Jyonson, a 25% aqueous suspension of styrenated acrylic copolymer resin) 30〃 100〃 Further below A multidentate ligand compound solution was prepared by blending.
オルソフエナントロリン 30部
イソプロピルアルコール 70〃
100〃
上記した水性オーバーコーテイング液(A液)
に多座配位子化合物溶液を2%添加し水性オーバ
ーコーテイング液(B液)を作成した。次に上記
した酸化重合型インキを43.5Kg/4.6判トツプコ
ート紙(神崎製紙製)にRIテスター(明製作所
製)を使用し、4分割ローラーにて0.2c.c.盛りで
ベタ刷り印刷し、直後に水性オーバーコーテイン
グ液のA液とB液とを、それぞれハンドプルーフ
アー(パマルコ社製)にて約4g/m2(液基準)
の割合で塗布した後、乾燥試験機(東洋精機製作
所製)にかけて乾燥時間を測定し、比較した。乾
燥時間は、A液を塗布した場合が3時間50分に対
しB液では、1時間40分であつた。 Orthophenanthroline 30 parts Isopropyl alcohol 70〃 100〃 The above aqueous overcoating liquid (Liquid A)
A 2% polydentate ligand compound solution was added to the solution to prepare an aqueous overcoating solution (solution B). Next, the above-mentioned oxidative polymerization type ink was printed solidly on 43.5 kg / 4.6 size top coated paper (manufactured by Kanzaki Paper Industries) using an RI tester (manufactured by Mei Seisakusho) with a 4-part roller in 0.2 cc increments, and immediately after the water-based The overcoating liquids A and B were each weighed at approximately 4 g/m 2 (liquid standard) using a hand proofing furnace (manufactured by Pamarco).
After coating at a ratio of , the drying time was measured using a drying tester (manufactured by Toyo Seiki Seisakusho) and compared. The drying time was 3 hours and 50 minutes when liquid A was applied, whereas it was 1 hour and 40 minutes when liquid B was applied.
実施例 2
下記配合にて多座配位子化合物溶液を作成し
た。Example 2 A multidentate ligand compound solution was prepared using the following formulation.
ビピリジン 30部
エタノール 70〃
100〃
実施例1に記載の水性オーバーコーテイング液
(A液)に上記溶液を5%添加し水性オーバーコ
ーテイング液を作成した。これを用い実施例1と
同様にして、塗布し乾燥時間を測定した。その結
果乾燥時間は1時間10分であつた。 Bipyridine 30 parts Ethanol 70〃 100〃 5% of the above solution was added to the aqueous overcoating liquid (liquid A) described in Example 1 to prepare an aqueous overcoating liquid. Using this, the coating was applied in the same manner as in Example 1, and the drying time was measured. As a result, the drying time was 1 hour and 10 minutes.
実施例 3
下記配合にて多座配位子化合物溶液を作成し
た。Example 3 A multidentate ligand compound solution was prepared using the following formulation.
フタラジン 20部
イソプロピルアルコール 80〃
100〃
実施例1に記載の水性オーバーコーテイング液
(A液)に上記添加液を5%添加したものを用い
実施例1と同様にして、塗布し乾燥時間を測定し
た。その結果、乾燥時間は2時間15分であつた。
さらに印刷2時間後500g/cm2の力を加え断裁時の
コスレ、製本時のコスレの度合を判定した所A液
を塗布したものはキズ跡が残つたのに対して、B
液を塗布したものは全つたくキズ跡が認められな
かつた。 Phthalazine 20 parts Isopropyl alcohol 80〃 100〃 5% of the above additive liquid was added to the aqueous overcoating liquid (liquid A) described in Example 1 and applied in the same manner as in Example 1, and the drying time was measured. . As a result, the drying time was 2 hours and 15 minutes.
Furthermore, after 2 hours of printing, a force of 500 g/cm 2 was applied to determine the degree of wrinkles during cutting and binding.The paper coated with liquid A left scratch marks, while the paper coated with liquid A left scratches.
All the items to which the liquid was applied were completely sticky and no scratch marks were observed.
Claims (1)
上に塗布するための水性オーバーコーテイング液
組成物であつて、水または水とアルコールとの混
合物を主要成分として含有してなる水性媒体中
に、前記脂肪酸の金属塩と反応して錯体を形成し
得る多座配位子化合物を分散させてなることを特
徴とする、水性オーバーコーテイング液組成物。1. An aqueous overcoating liquid composition for coating on a wet film of an oil-based ink containing a metal salt of a fatty acid, in an aqueous medium containing water or a mixture of water and alcohol as a main component. 1. An aqueous overcoating liquid composition comprising a polydentate ligand compound capable of reacting with the metal salt of the fatty acid to form a complex.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56051401A JPS57165294A (en) | 1981-04-06 | 1981-04-06 | Composition of water overcoating liquid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56051401A JPS57165294A (en) | 1981-04-06 | 1981-04-06 | Composition of water overcoating liquid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57165294A JPS57165294A (en) | 1982-10-12 |
| JPS64240B2 true JPS64240B2 (en) | 1989-01-05 |
Family
ID=12885915
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56051401A Granted JPS57165294A (en) | 1981-04-06 | 1981-04-06 | Composition of water overcoating liquid |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57165294A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20190293362A1 (en) * | 2018-03-26 | 2019-09-26 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| US10859319B2 (en) | 2018-02-05 | 2020-12-08 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| EP3809083A1 (en) | 2019-10-17 | 2021-04-21 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| EP3816563A1 (en) | 2019-10-31 | 2021-05-05 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| EP3882553A1 (en) | 2020-03-17 | 2021-09-22 | Shinko Electric Industries Co., Ltd. | Loop heat pipe and method for manufacturing loop heat pipe |
| US11131509B2 (en) | 2018-02-05 | 2021-09-28 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| EP3896381A1 (en) | 2020-04-17 | 2021-10-20 | Shinko Electric Industries Co., Ltd. | Loop heat pipe and method for manufacturing loop heat pipe |
| EP4043822A1 (en) | 2021-02-12 | 2022-08-17 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6042097A (en) * | 1983-08-19 | 1985-03-06 | Sakata Shokai Ltd | Aqueous overcoating composition and printing method using the same |
| JPS6070415A (en) * | 1983-09-28 | 1985-04-22 | Sakata Shokai Ltd | Aqueous overcoating composition and printing method using it |
-
1981
- 1981-04-06 JP JP56051401A patent/JPS57165294A/en active Granted
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10859319B2 (en) | 2018-02-05 | 2020-12-08 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| US11131509B2 (en) | 2018-02-05 | 2021-09-28 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| US20190293362A1 (en) * | 2018-03-26 | 2019-09-26 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| EP3809083A1 (en) | 2019-10-17 | 2021-04-21 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| EP3816563A1 (en) | 2019-10-31 | 2021-05-05 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| EP3882553A1 (en) | 2020-03-17 | 2021-09-22 | Shinko Electric Industries Co., Ltd. | Loop heat pipe and method for manufacturing loop heat pipe |
| US11808521B2 (en) * | 2020-03-17 | 2023-11-07 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
| EP3896381A1 (en) | 2020-04-17 | 2021-10-20 | Shinko Electric Industries Co., Ltd. | Loop heat pipe and method for manufacturing loop heat pipe |
| EP4043822A1 (en) | 2021-02-12 | 2022-08-17 | Shinko Electric Industries Co., Ltd. | Loop heat pipe |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57165294A (en) | 1982-10-12 |
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