JPH0197298A - Coating composition for press processing - Google Patents
Coating composition for press processingInfo
- Publication number
- JPH0197298A JPH0197298A JP25304887A JP25304887A JPH0197298A JP H0197298 A JPH0197298 A JP H0197298A JP 25304887 A JP25304887 A JP 25304887A JP 25304887 A JP25304887 A JP 25304887A JP H0197298 A JPH0197298 A JP H0197298A
- Authority
- JP
- Japan
- Prior art keywords
- resin dispersion
- press processing
- weight
- aqueous resin
- gloss
- 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
- 238000012545 processing Methods 0.000 title claims description 24
- 239000008199 coating composition Substances 0.000 title claims description 13
- 239000011347 resin Substances 0.000 claims abstract description 51
- 229920005989 resin Polymers 0.000 claims abstract description 51
- 239000006185 dispersion Substances 0.000 claims abstract description 42
- 239000000178 monomer Substances 0.000 claims abstract description 23
- 230000009477 glass transition Effects 0.000 claims abstract description 14
- 239000011256 inorganic filler Substances 0.000 claims abstract description 10
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 23
- 229920002554 vinyl polymer Polymers 0.000 claims description 20
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 15
- 239000003995 emulsifying agent Substances 0.000 claims description 7
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 5
- 229920000178 Acrylic resin Polymers 0.000 claims description 3
- 239000004925 Acrylic resin Substances 0.000 claims description 3
- 229920005792 styrene-acrylic resin Polymers 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract description 10
- 239000000203 mixture Substances 0.000 abstract description 10
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract description 9
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000843 powder Substances 0.000 abstract description 4
- 230000000903 blocking effect Effects 0.000 abstract description 3
- 239000003054 catalyst Substances 0.000 abstract description 3
- 239000000377 silicon dioxide Substances 0.000 abstract description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 abstract description 2
- 239000010453 quartz Substances 0.000 abstract description 2
- 239000004615 ingredient Substances 0.000 abstract 2
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- 238000004519 manufacturing process Methods 0.000 description 12
- 239000002270 dispersing agent Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000000123 paper Substances 0.000 description 8
- -1 S-butyl Chemical group 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000003825 pressing Methods 0.000 description 6
- 238000007639 printing Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000003475 lamination Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 229920001800 Shellac Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000006082 mold release agent Substances 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 2
- 239000004208 shellac Substances 0.000 description 2
- 229940113147 shellac Drugs 0.000 description 2
- 235000013874 shellac Nutrition 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 229920005731 JONCRYL® 67 Polymers 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 238000007766 curtain coating Methods 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 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
- 238000009472 formulation Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 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 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- UTSYWKJYFPPRAP-UHFFFAOYSA-N n-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCNC(=O)C=C UTSYWKJYFPPRAP-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- HXHCOXPZCUFAJI-UHFFFAOYSA-N prop-2-enoic acid;styrene Chemical compound OC(=O)C=C.C=CC1=CC=CC=C1 HXHCOXPZCUFAJI-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
- Paper (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、プレス加工用の被覆剤に関し、特に光沢、平
滑性、耐摩擦性、接着性並びに耐ブロッキング性、作業
性に優れ、かつコルゲータ−適性、耐熱性に優れたプレ
ス加工用の被覆剤組成物を提供しようとするものである
。Detailed Description of the Invention <Industrial Application Field> The present invention relates to a coating material for press working, which has particularly excellent gloss, smoothness, abrasion resistance, adhesion and blocking resistance, and workability, and which is suitable for corrugators. - It is an object of the present invention to provide a coating composition for press processing that has excellent suitability and heat resistance.
〈従来の技術〉
近年、印刷物の美粧化、高級化指向から印刷面の上から
、樹脂溶液を塗布、乾燥せしめ、ついで鏡面板を用いて
ホットプレスすることにより、光沢は与を行うことが広
く行われている。<Conventional technology> In recent years, in order to make printed matter more beautiful and more sophisticated, it has become common practice to apply a resin solution onto the printed surface, dry it, and then hot press it using a mirror plate to impart gloss. It is being done.
従来、この種のプレス加工は、本やマツチの表紙、カレ
ンダーあるいは、化粧箱などの分野が中心であったが、
段ボールの分野においても美粧化、高級化の請求が高ま
り、高度な光沢を有する美粧段ボールの用途が拡大しつ
つある状況にある。Traditionally, this type of press processing was mainly used for the production of book and Matsushi covers, calendars, and gift boxes.
In the field of corrugated cardboard as well, there is an increasing demand for decorative and high-grade corrugated cardboard, and the use of highly glossy decorative corrugated cardboard is expanding.
プレス加工方法は、印刷された紙に、樹脂溶液を塗布、
乾燥した後、平圧プレスもしくはエンドレスプレスにて
、加圧して光沢付与を行うものであるため、表ライナ−
、中芯、裏ライナーとを貼合した後の段ボールの場合は
、段っぷれが生じ、プレス加工は出来ないものである。The press processing method involves applying a resin solution to the printed paper.
After drying, the surface liner is applied with a flat press or an endless press to give it gloss.
In the case of corrugated board after pasting together the core and back liner, undulations occur and press processing cannot be performed.
それゆえ高度な光沢を有する段ボールを得ようとすれば
、予めプレス加工を行った印刷物を段ボールに貼り合わ
せる方法もしくは、表ライナーの印刷物をプレス加工し
た後、コルゲータ−マシーンでもって中芯及び裏ライナ
ーと貼り合わせる方法のどちらかの方法を取らざるを得
ないものであった。Therefore, if you want to obtain corrugated board with a high level of gloss, you can either attach pre-pressed printed matter to the corrugated board, or press the front liner printed matter and then use a corrugator machine to attach the center core and back liner. There was no choice but to use one of two methods: pasting it together.
しかし、前者の場合は、段ボールにプレス加工を行った
印刷物を貼り合わせるものであるため、特別な貼り合わ
せ機が必要となり、また、作業効率が低いという問題が
予想され、後者の場合は、コルゲータ−マシーンにおけ
る貼り合わせ温度(通常160〜190℃で行われる)
に対する適性あるいは高温となった熱板との接触摩擦に
対する適性が要求されるものである。However, in the former case, a special pasting machine is required because printed materials are pasted together by press processing on cardboard, and the problem of low work efficiency is expected; in the latter case, corrugator - Bonding temperature in the machine (usually done at 160-190°C)
or contact friction with a hot plate.
従来のプレス加工においては、印刷紙の上に塗布して得
られた樹脂面にステンレス製等の鏡面板を重ね、平圧プ
レスを行うかあるいは、鏡面加工を行ったエンドレスベ
ルト等を用いてホットローラー間を通すことによって、
連続的に光沢付与のためのプレス加工が行われるが、こ
のときの温度は、通常90〜130℃の範囲で行われる
ため、前述コルゲータ−の貼り合わせ温度とは比べもの
にならないほど低いものであり、かつ、この温度範囲で
軟化するような樹脂溶液が使用されていたものである。In conventional press processing, a mirror plate made of stainless steel or the like is layered on the resin surface obtained by applying it onto printing paper, and flat pressure pressing is performed, or hot printing is performed using an endless belt etc. that has been subjected to mirror finishing. By passing it between rollers,
Press processing is performed continuously to impart gloss, but the temperature at this time is usually in the range of 90 to 130°C, which is far lower than the corrugator bonding temperature mentioned above. , and a resin solution that softens within this temperature range was used.
これら従来のプレス加工用の被覆剤としては溶剤型の塩
化ビニル−酢酸ビニル系樹脂からなるものく特開昭50
−12312号等)が広く使用されていたが、作業環境
問題、火災の危険性の問題から、最近では水性タイプに
変更して来ておりアクリル系又はスチレン系の共重合体
の水性分散物あるいは、これに池の水溶性高分子を混合
せしめた被覆剤(特開昭50−148607号、51−
82010号、51−82011号)などが知られてい
る。これら被覆剤には、前記樹脂以外に光沢を向上させ
るための材料としてレベリング剤、可塑剤など、あるい
は、剥離を容易にするための剥離剤などの添加は必要に
応じて行われているが、シリカのような無機充填剤は、
光沢向上にはマイナスに作用するものであるため使用さ
れていないものであった。Conventional coating materials for press processing include solvent-based vinyl chloride-vinyl acetate resins.
-12312, etc.), but due to work environment problems and fire hazards, recently it has been changed to water-based types, and water-based dispersions of acrylic or styrene copolymers or , a coating agent in which a water-soluble polymer of Ike was mixed (JP-A-50-148607, 51-
No. 82010, No. 51-82011), etc. are known. In addition to the above-mentioned resins, leveling agents, plasticizers, etc. are added to these coating materials as necessary to improve gloss, or release agents are added to facilitate peeling. Inorganic fillers such as silica
It was not used because it had a negative effect on improving gloss.
〈発明が解決しようとする問題点〉
従来の水性タイプのプレス加工用被覆剤を使用して、予
め印刷された段ボールの表ライナーに塗布し、乾燥後、
ロールプレスによりプレス加工を行った表ライナーを用
いて、中芯及び裏ライナーとの貼合をコルゲータ−マシ
ーンで行った場合、貼合の温度である160〜190℃
で再軟化し、光沢の劣化が起こったり、再軟化した樹脂
が熱板汚れを生じ、段ボールの商品価値を著しく低下さ
せるという問題を有することがわかった。従って、従来
のプレス加工用の被覆剤では、コルゲータ−マシーン等
の高熱には耐えることが出来ないものであった。<Problems to be Solved by the Invention> A conventional water-based press coating is applied to the front liner of a pre-printed corrugated board, and after drying,
When using a front liner that has been pressed using a roll press and laminating it with the core and back liner using a corrugator machine, the lamination temperature is 160 to 190°C.
It has been found that there are problems in that the re-softened resin deteriorates the gloss and the re-softened resin stains the hot plate, significantly reducing the commercial value of the corrugated board. Therefore, conventional coating materials for press working cannot withstand the high heat of corrugator machines and the like.
この対策として、被覆剤に使用する樹脂として、軟化点
の高いものを使用して、コルゲータ−マシーンでの耐熱
性を向上させることも考えられるが、この場合は、プレ
スローラーの温度もそれだけ高くしなければならないば
かりか、プレス加工時の高温化によって紙の収縮が生じ
、裁断の時のゲントのずれの原因となったり、紙の強度
劣化、更にはシートのそりが発生するなど、段ボールの
製造には問題となるものであった。As a countermeasure to this problem, it may be possible to improve the heat resistance of the corrugator machine by using a resin with a high softening point for the coating material, but in this case, the temperature of the press roller should also be raised accordingly. Not only that, but the high temperature during press processing causes the paper to shrink, causing paper to shift during cutting, deteriorating the strength of the paper, and even warping the sheets. This was a problem.
本発明は、プレス加工における温度を特別に高温にする
ことなく、従来の温度でもって、光沢付与が出来、かつ
コルゲータ−マシーンでの貼合においても光沢低下等の
問題が発生しないプレス加工用被覆剤組成物を提供する
ことを目的とする。The present invention provides a coating for press processing that can be applied at conventional temperatures without raising the temperature during press processing to a particularly high temperature, and that does not cause problems such as reduction in gloss even when laminated using a corrugator machine. The purpose of the present invention is to provide a drug composition.
く問題を解決するための手段〉
本発明者らは、プレス加工により光沢を付与した後にお
いて、コルゲータ−マシーンの貼合工程を通過させても
光沢低下、あるいは熱板汚れ等の問題の発生しない、高
度な光沢を有する段ボール製造に適したプレス加工用被
覆剤組成物について鋭意研究を重ねた結果、特定範囲の
ガラス転移温度を有する水性樹脂分散物に特定範囲の割
合の無機充填剤を混合せしめることによって、高度な光
沢付与が出来ると同時に、上記貼合工程のような温度か
つ熱板接触、摩擦というような過激な条件にさらされて
も光沢低下等の問題が発生しないことを見い出し、本発
明を完成するに至ったものである。Means for Solving the Problems> The present inventors have developed a method that does not cause problems such as a decrease in gloss or staining of hot plates even if it is passed through the lamination process of a corrugator machine after imparting gloss through press working. As a result of extensive research into a coating composition for press processing suitable for producing highly glossy corrugated board, we have developed an aqueous resin dispersion with a glass transition temperature within a specific range, mixed with an inorganic filler in a specific range of proportions. We discovered that this method enables a high level of gloss to be imparted, and at the same time does not cause problems such as loss of gloss even when exposed to extreme conditions such as temperature, hot plate contact, and friction as in the above-mentioned lamination process. This led to the completion of the invention.
すなわち、本発明は、ガラス転移温度(Tg)が60〜
130℃の範囲にある水性樹脂分散物と、無機充填剤を
主成分とするプレス加工用被覆剤組成物を提供しようと
するものである。That is, the present invention has a glass transition temperature (Tg) of 60 to
It is an object of the present invention to provide a coating composition for press processing which contains an aqueous resin dispersion having a temperature range of 130°C and an inorganic filler as main components.
まず、本発明に係る組成物に使用する特定のガラス転移
温度を有する水性樹脂分散物を得るに際しては、以下例
示するビニルモノマーのホモポリマーのガラス転移温度
を考慮し、従来公知の近似式等に基づき、それぞれ使用
するビニルモノマーの重合割合を設定することによって
、目的とするガラス転移温度を有する水性樹脂分散物を
得ることが出来る。一方、比較的高いTgの重合体から
なる水性樹脂分散物と、比較的低いTgの重合体からな
る水性樹脂分散物とを混合せしめた、いわゆるポリマー
ブレンドによっても目的とするTgの水性樹脂分散物を
得ることが出来る。本発明に係る水性樹脂分散物を製造
するに使用出来るビニルモノマーとしては、以下のもの
が例示される。First, when obtaining an aqueous resin dispersion having a specific glass transition temperature to be used in the composition according to the present invention, consider the glass transition temperature of the vinyl monomer homopolymer shown below, and use the conventionally known approximate formula etc. By setting the polymerization ratio of each vinyl monomer based on the above, an aqueous resin dispersion having a desired glass transition temperature can be obtained. On the other hand, a so-called polymer blend, which is a mixture of an aqueous resin dispersion made of a polymer with a relatively high Tg and an aqueous resin dispersion made of a polymer with a relatively low Tg, can also be used to obtain an aqueous resin dispersion with a desired Tg. can be obtained. Examples of vinyl monomers that can be used to produce the aqueous resin dispersion according to the present invention include the following.
比較的高いTgのホモポリマーを得ることが出来るビニ
ルモノマーとしては、アクリル酸、メタクリル酸、メタ
クリレート、エチルメタクリレート等のアクリル系ビニ
ルモノマー及びスチレン、α−メチルスチレン等のスチ
レン系ビニルモノマーがあり、また、比較的低いTgの
ビニルモノマーとしては、上記、メチルメタクリレート
及びエチルメタクリレート以外のアクリル酸又はメタク
リル酸アルキルエステル例えばメチル、エチル、プロピ
ル、イソプロピル、n−ブチル、S−ブチル、t−ブチ
ル、ヘキシル、2−エチルヘキシル、デシル、ラウリル
、等の直鎖又は側鎖のアルキル基を有するエステルを例
示することが出来る。なお、前述モノマー以外に他のビ
ニルモノマーを共重合させることも可能で、クロトン酸
など不飽和モノカルボン酸、イタコン酸、フマール酸、
マレイン酸なとのα、β不飽和ジカルボン酸、N−メ千
ロールアクリルアミド、N−ブトキシメチルアクリルア
ミドなどの少なくとも1個のN−置換メチロール基を含
有するアクリル酸アミド誘導体、エチレングリコール、
ジエチレングリコール、プロピレングリコール、ジプロ
ピレングリコールなどのグリコール類のアクリル酸もし
くはメタクリル酸のモノ、又は、ジエステル類、あるい
はアクリル酸、メタクリル酸のグリシジルエーテルなど
の七ツマ−あるいは、アクリロニトリル、塩化ビニル、
酢酸ビニル、プロピオン酸ビニル、塩化ビニリデンなど
を例示することが出来る。Vinyl monomers from which homopolymers with relatively high Tg can be obtained include acrylic vinyl monomers such as acrylic acid, methacrylic acid, methacrylate, and ethyl methacrylate, and styrene vinyl monomers such as styrene and α-methylstyrene. Examples of vinyl monomers with relatively low Tg include acrylic acid or methacrylic acid alkyl esters other than methyl methacrylate and ethyl methacrylate, such as methyl, ethyl, propyl, isopropyl, n-butyl, S-butyl, t-butyl, hexyl, Examples include esters having a linear or side chain alkyl group such as 2-ethylhexyl, decyl, and lauryl. In addition to the above-mentioned monomers, it is also possible to copolymerize other vinyl monomers, such as unsaturated monocarboxylic acids such as crotonic acid, itaconic acid, fumaric acid,
alpha, beta unsaturated dicarboxylic acids such as maleic acid, acrylamide derivatives containing at least one N-substituted methylol group such as N-methylol acrylamide, N-butoxymethyl acrylamide, ethylene glycol,
Mono- or diesters of acrylic acid or methacrylic acid of glycols such as diethylene glycol, propylene glycol, and dipropylene glycol, or monomers such as glycidyl ether of acrylic acid and methacrylic acid, acrylonitrile, vinyl chloride,
Examples include vinyl acetate, vinyl propionate, and vinylidene chloride.
これら例示したビニルモノマーのうちでも、アクリル酸
又はメタクリル酸もしくは、それらのアルキルエステル
類及びスチレン系ビニルモノマーを主成分とするものが
好適である。Among these exemplified vinyl monomers, those whose main components are acrylic acid, methacrylic acid, or their alkyl esters, and styrene vinyl monomers are preferred.
これらビニルモノマーから水性樹脂分散物を得るには前
述上ツマ−を過硫酸アンモニウム、過硫酸カリウム、過
酸化水素水などの親水性触媒あるいは、レドックス系触
媒を用いて一般公知の方法で乳化重合し安定に分散せし
めればよく、必要に応じ乳化剤を加えることも出来る。To obtain an aqueous resin dispersion from these vinyl monomers, the above-mentioned polymers are stabilized by emulsion polymerization using a hydrophilic catalyst such as ammonium persulfate, potassium persulfate, hydrogen peroxide, or a redox catalyst using a generally known method. What is necessary is to disperse the emulsifier into a mixture, and if necessary, an emulsifier can be added.
これら、乳化剤として、アニオンあるいはノニオン系界
面活性剤の存在下ビニルモノマーの混合物を乳化状態で
共重合せしめれば良いが、一般的に低分子活性剤の使用
は、生成被膜の耐水性等に悪い影響を及ぼす場合がある
ので、耐水性が特に要求される場合には高分子アニオン
系活性剤が乳化剤として好適である。As an emulsifier, a mixture of vinyl monomers can be copolymerized in an emulsified state in the presence of an anionic or nonionic surfactant, but in general, the use of low-molecular-weight surfactants is bad for the water resistance of the resulting film. Therefore, when water resistance is particularly required, polymeric anionic activators are suitable as emulsifiers.
本発明に係る水性樹脂分散物も係る乳化剤を使用するこ
とによって優れた性能を有するものとなる。かかる高分
子乳化剤としては、シェラツク、カルボキシル基を有す
る(メタ)アクリル酸系又はマレイン酸系共重合体等、
従来のアルカリ可溶性樹脂の水溶液が使用出来る。The aqueous resin dispersion according to the present invention also has excellent performance by using the emulsifier. Such polymer emulsifiers include shellac, (meth)acrylic acid-based or maleic acid-based copolymers having carboxyl groups, etc.
Conventional aqueous solutions of alkali-soluble resins can be used.
本発明に係るプレス加工用被覆剤組成物に関しては、比
較的高いガラス転移温度(60〜130℃)を有する水
性樹脂分散物を使用することが必要であるため、実施例
に示す如く、乳化重合の際使用する分散剤として、アク
リル酸、メタクリル酸、スチレン等の高いガラス転移温
度のホモボリマーを形成するビニルモノマーから構成さ
れるアルカリ可溶性樹脂の水溶液を比較的多量に使用し
て、常法により他のビニルモノマーを乳化重合せしめた
ものが好適である。Regarding the coating composition for press processing according to the present invention, it is necessary to use an aqueous resin dispersion having a relatively high glass transition temperature (60 to 130°C). As a dispersant used in this process, a relatively large amount of an aqueous solution of an alkali-soluble resin composed of a vinyl monomer that forms a homopolymer with a high glass transition temperature, such as acrylic acid, methacrylic acid, or styrene, is used, and other It is preferable to emulsion polymerize vinyl monomers.
アルカリ可溶性樹脂の水溶化のため使用するアルカリと
しては、公知のものを使用出来、アンモニア、有機アミ
ン、例えばトリエタノールアミン、モノエタノールアミ
ン等が挙げられるが水溶性樹脂の乾燥の上から揮発性の
高いアルカリが良い。As the alkali used for water-solubilizing the alkali-soluble resin, any known alkali can be used, such as ammonia, organic amines such as triethanolamine, monoethanolamine, etc. However, after drying the water-soluble resin, volatile High alkalinity is good.
ここで、得られた水溶性樹脂分散物のTgが60℃未満
では耐熱性が充分でなく、コルゲータ−マシーンでの貼
合において、光沢低下、もしくは、熱板汚れが生じるこ
ととなり、Tgが130℃を超えるとプレス加工で塗膜
のつぶれ性が充分得られず、目的とする高い光沢(通常
、高い光沢を有するものは、グロスメーターで、70℃
以上のものを言い、超光沢を有するものは、80〜85
℃のものを言う。)が得にくくなるものである。Here, if the Tg of the obtained water-soluble resin dispersion is less than 60°C, the heat resistance will not be sufficient, and during lamination with a corrugator machine, gloss will decrease or hot plate stains will occur. C
Those with super gloss are 80 to 85
Say something at ℃. ) becomes difficult to obtain.
他の一方の必須成分である無機充填剤としては、シリカ
粉末、シリカゲル、石英パウダー、アルミナ、ガラス粉
末、タルク、クレー、炭酸カルシウム、炭酸マグネシウ
ム、亜鉛華、硫酸バリウムなどが例示でき、本発明の被
覆組成物中、0.1〜5.0重量%、より好ましくは、
0.5〜3.0重量%の範囲で含有せしめることが必要
である。無機充填剤の含有量が、0,1重量%未満であ
る場合は、耐熱性のうえで充分でなく、逆に5.0%を
超えると、高度な光沢が得られないという問題が発生す
るものである。Examples of the inorganic filler which is the other essential component include silica powder, silica gel, quartz powder, alumina, glass powder, talc, clay, calcium carbonate, magnesium carbonate, zinc white, barium sulfate, etc. In the coating composition, 0.1 to 5.0% by weight, more preferably,
It is necessary to contain it in a range of 0.5 to 3.0% by weight. If the content of the inorganic filler is less than 0.1% by weight, the heat resistance will not be sufficient, and if it exceeds 5.0%, there will be a problem that high gloss cannot be obtained. It is something.
本発明に係るプレス加工用の被覆剤組成物を製造する場
合は、前述水性樹脂分散物中に上記無機充填剤を混合し
て得るか、あるいは、通常の分散機を用いて微細に分散
せしめることによって得ることが出来る。When producing the coating composition for press processing according to the present invention, the inorganic filler may be mixed into the aqueous resin dispersion, or finely dispersed using a conventional dispersion machine. It can be obtained by
なお、組成物中には、必要に応じ以下の添加剤を加える
ことが可能であり、それら添加剤としては、印刷面への
接着性を補助するための水溶性フェスがあり、アクリル
系樹脂、ロジン変性マレイン酸樹脂、スチレン−マレイ
ン酸樹脂、シェラツク等のアルカリ可溶剤樹脂の水溶液
を添加することが出来る。また、耐摩擦性を向上するた
めのポリエチレン系等のワックス類、プレス加工時の剥
離性を向上させる目的でステアリン酸の如き高級脂肪酸
、セチルアルコールの如き高級アルコール、リン酸エス
テルのような界面活性剤等が使用出来る。In addition, the following additives can be added to the composition as necessary, and these additives include water-soluble face to assist in adhesion to the printed surface, acrylic resin, An aqueous solution of an alkali-soluble resin such as a rosin-modified maleic resin, a styrene-maleic resin, or shellac can be added. In addition, waxes such as polyethylene waxes are used to improve abrasion resistance, higher fatty acids such as stearic acid, higher alcohols such as cetyl alcohol, and surfactants such as phosphoric acid esters are used to improve peelability during press processing. Agents etc. can be used.
また、添加剤として、染料、顔料等の着色剤を添加する
ことも可能で有色の光沢被膜を得ることも可能となる。It is also possible to add colorants such as dyes and pigments as additives, making it possible to obtain a colored glossy film.
以上のような成分から成るプレス加工用被覆剤を塗布す
る対象としては、通常の段ボール製造に使用されるライ
ナー紙、例えばジュートライナー、Kライナーでも良い
が、表面平滑性に優れるコートボール紙が好ましく、こ
れらに対して、フレキソインキ、平版インキもしくはグ
ラビアインキ等を用いて巻取り形式で印刷されたもので
あり、ロールコート、カーテンコート、スプレーコート
あるいは、グラビア印刷機などの手段を用いて、全面又
は必要部分に塗布される。塗布後、乾燥し、プレス加工
に使用するホットローラーでもって光沢付与を行う。The material to which the press processing coating consisting of the above-mentioned components is applied may be liner paper used in normal corrugated board manufacturing, such as jute liner or K liner, but coated cardboard with excellent surface smoothness is preferable. , these are printed in roll format using flexo ink, planographic ink, gravure ink, etc., and are printed on the entire surface using means such as roll coating, curtain coating, spray coating, or gravure printing machine. Or apply it to the necessary areas. After application, it is dried and then glossed using a hot roller used for press processing.
ホットローラーの温度としては、90〜130℃の範囲
で圧力 !50〜350 Kg/crr?で行うことが
出来る。The temperature of the hot roller should be between 90 and 130 degrees Celsius, and the pressure should be within the range of 90 to 130 degrees. 50~350 Kg/crr? It can be done with.
プレス加工により光沢を付与された表ライナーは、段ボ
ール製造のためのコルゲータ−マシーンの表ライナー用
ミルスタンドに設置し、従来と同じ方法で、中芯、裏ラ
イナーと貼合することによって、高い光沢を有する段ボ
ールを得ることが出来るものである。The front liner, which has been given a gloss by pressing, is installed on the mill stand for the front liner of a corrugator machine for manufacturing corrugated board, and is bonded to the core and back liner using the same method as before to achieve high gloss. It is possible to obtain corrugated cardboard having the following characteristics.
中芯、裏ライナーと貼合された光沢を有する段ボールは
、印刷模様、あるいは、段ボールの大きさに従い裁断さ
れ、しかる後、必要なダイカッティング等を行い、段ボ
ール箱として使用するものである。The glossy corrugated board bonded to the core and back liner is cut according to the printed pattern or the size of the corrugated board, and then subjected to necessary die-cutting and the like to be used as a corrugated box.
以下、実施例でもって、本発明に係るプレス加工用被覆
剤組成物を具体的に説明するが、これに限定されるもの
ではない。Hereinafter, the press working coating composition according to the present invention will be specifically explained with reference to Examples, but the present invention is not limited thereto.
〈実施例〉
分散物製造例1
メタクリ、ル酸53重量%、メチルメタクリレート23
重量%、スチレン24重量%からなるアルカリ可溶性樹
脂のアンモニア水溶液を分散剤として用い、分散剤の樹
脂分66重量部に対して、スチレン34重量部を添加し
、常法4’AL化重合し、水性樹脂分散物Aを得る。得
られた分散物Aは、固形分37重量%、分散物のガラス
転移温度、約125℃である。<Example> Dispersion production example 1 Methacrylic acid, 53% by weight of lactic acid, methyl methacrylate 23%
Using an ammonia aqueous solution of an alkali-soluble resin containing 24% by weight of styrene as a dispersant, 34 parts by weight of styrene was added to 66 parts by weight of the resin content of the dispersant, and 4'AL polymerization was carried out in a conventional manner. Aqueous resin dispersion A is obtained. The obtained dispersion A has a solid content of 37% by weight and a glass transition temperature of the dispersion of about 125°C.
分散物製造例2
製造例1と同様、メタクリル酸36重量%、メチルメタ
クリレート49重量%、ブチルアクリレート15重量%
、からなるアルカリ可溶性樹脂のアンモニア水溶液を分
散剤として用い、分散剤の樹脂分60重量部に対して、
スチレン33重量部、ブチルアクリレート7重量部を常
法により乳化重合し、水性樹脂分散物Bを得る。得られ
た分散物Aは、固形分39重量%、ガラス転移温度、約
76℃の分散物である。Dispersion Production Example 2 Same as Production Example 1, 36% by weight of methacrylic acid, 49% by weight of methyl methacrylate, 15% by weight of butyl acrylate.
Using an ammonia aqueous solution of an alkali-soluble resin consisting of as a dispersant, with respect to 60 parts by weight of the resin content of the dispersant,
Aqueous resin dispersion B is obtained by emulsion polymerization of 33 parts by weight of styrene and 7 parts by weight of butyl acrylate by a conventional method. The resulting dispersion A has a solid content of 39% by weight and a glass transition temperature of about 76°C.
分散物製造例3
製造例1と同様、メタクリル酸28重量%、アクリル酸
4重量%、メタクリレート 7重量%、エチルアクリレ
−)61重量4==u%、からなるアルカリ可溶性樹脂
のアンモニア水溶液を分散剤として使用し、分散剤の樹
脂分12重量部に対して、スチレン移温度、約89℃の
分散物である。Dispersion Production Example 3 As in Production Example 1, an ammonia aqueous solution of an alkali-soluble resin consisting of 28% by weight of methacrylic acid, 4% by weight of acrylic acid, 7% by weight of methacrylate, and 4% by weight of ethyl acrylate was used as a dispersant. It is a dispersion with a styrene transition temperature of about 89°C based on 12 parts by weight of the resin content of the dispersant.
分散物製造例4
アルカリ可溶性樹脂として、アクリル樹脂(ジョンクリ
ル67)を使用し、そのアルカリ水溶液を分散剤として
使用する。分散剤の樹脂分、10重量部に対して、イソ
ブチルメタクリレート54重量部、スチレン36重量部
を常法により乳化重合せしめ水性樹脂分散物りを得る。Dispersion Production Example 4 Acrylic resin (Joncryl 67) is used as the alkali-soluble resin, and its alkaline aqueous solution is used as the dispersant. To 10 parts by weight of the resin component of the dispersant, 54 parts by weight of isobutyl methacrylate and 36 parts by weight of styrene are emulsion polymerized by a conventional method to obtain an aqueous resin dispersion.
分散物りの固形分は、40重量%、ガラス転移温度、約
67℃である。The solids content of the dispersion is 40% by weight and the glass transition temperature is about 67°C.
分散物製造例5
アクリル酸29重量%、スチレン12重量%、α−メチ
ルスチレン56重量%、エチルジグリコールアクリレー
ト3重量%からなるアルカリ可溶性樹脂のアンモニア水
溶液を分散剤として用い、分散剤の樹脂分30重量部に
対して、スチレン20重量部、2−エチルへキシルアク
リレート 50重量部を乳化重合せしめ、水性樹脂分散
物Eを得る。得られた分散物Eは、固形分45重置火、
ガラス転移温度、約40℃の分散物である。Dispersion Production Example 5 An ammonia aqueous solution of an alkali-soluble resin consisting of 29% by weight of acrylic acid, 12% by weight of styrene, 56% by weight of α-methylstyrene, and 3% by weight of ethyldiglycol acrylate was used as a dispersant, and the resin content of the dispersant was Aqueous resin dispersion E is obtained by emulsion polymerization of 20 parts by weight of styrene and 50 parts by weight of 2-ethylhexyl acrylate with respect to 30 parts by weight. The obtained dispersion E had a solid content of 45 times,
It is a dispersion with a glass transition temperature of about 40°C.
実施例1〜10、比較例1〜5
分散物製造例1〜5で得た分散物A〜Eを使用し、表−
1に示した配合に基づき、プレス加工用被覆剤を調整す
る。Examples 1 to 10, Comparative Examples 1 to 5 Using dispersions A to E obtained in Dispersion Production Examples 1 to 5, Table-
A coating material for press processing is prepared based on the formulation shown in 1.
なお、表中の数字は重量部を示し、ワックスとしては、
ポリエチレンワックスを、離型剤としては、リン酸エス
テル系離型剤を使用する。In addition, the numbers in the table indicate parts by weight, and as wax,
A phosphoric acid ester mold release agent is used as a mold release agent for polyethylene wax.
評価試験
段ボールライナー印刷用の2色印刷機を使用し、本州製
紙製UFマニラ紙(230g/m”)に水性フレキソイ
ンキを第1色目で、実施例1〜lO1及び比較例1〜5
のそれぞれの被覆剤を2色目として、連続印刷、塗布を
行う。乾燥後、エンドレスプレス機にて、温度130℃
、圧力3007 cm”で、30m/分のスピードでホ
ットローラーでプレス加工を行い光沢付与を行った。プ
レス加工後の光沢はグロスメーターで測定し、その測定
値を表−1に追記した。Evaluation Test Using a two-color printing machine for printing corrugated board liners, water-based flexographic ink was applied as the first color to Honshu Paper Industries' UF Manila paper (230 g/m'') for Examples 1 to 1O1 and Comparative Examples 1 to 5.
Continuous printing and application are performed using each coating material as the second color. After drying, use an endless press at a temperature of 130°C.
The gloss was imparted by pressing with a hot roller at a speed of 30 m/min under a pressure of 3007 cm'' and a speed of 30 m/min.The gloss after pressing was measured with a gloss meter, and the measured values were added to Table 1.
光沢を付与したライナーを表ライナーとして用い、コル
ゲータ−マシーンで中芯、裏ライナーとの貼合を行い、
段ボールで製造する。Using a glossy liner as the front liner, it is laminated with the core and back liner using a corrugator machine.
Manufactured from cardboard.
得られた段ボールについて、同様クロスメーターで測定
し、プレス加工後の光沢比すなわち光沢低下の程度を測
定する。The obtained corrugated board is similarly measured using a crossmeter to measure the gloss ratio after pressing, that is, the degree of gloss reduction.
また、コルゲータ−マシーンによる表面キズの発生の有
無、及び熱板汚れの有無を目視により判断する一方、裁
断した段ボールの積み上げによるブロッキングの発生の
有無を調べ、それぞれの結果を表−1に追記しな。In addition, we visually judged the presence of surface scratches caused by the corrugator machine and the presence of hot plate stains, and also examined the presence or absence of blocking caused by stacking cut cardboard, and added the results to Table 1. Na.
表−1中の注記は以下のものを示す。Notes in Table-1 indicate the following.
注1 ・・・・・・ シリカゲルとしてサイロイド63
(富士デビソン社製)を使用。Note 1 Thyroid 63 as silica gel
(manufactured by Fuji Davison).
注2 ・・・・・・ コロイダルシリカとして、スノー
テックスN(8産化学社製)
(固形分20%)を使用。Note 2: Snowtex N (manufactured by 8 San Kagaku Co., Ltd.) (solid content 20%) is used as colloidal silica.
注3 ・・・・・・ 炭酸カルシウムとして白艶華T−
DD (白石カルシューム社製)
(炭カル分50%)を使用。Note 3: Shiroenka T- as calcium carbonate
DD (manufactured by Shiraishi Calcium Co., Ltd.) (charcoal calcium content 50%) is used.
注4 ・・・・・・ 光沢比は、プレス加工後の光沢値
でもって、コルゲータ−マシ
ーン通過後の光沢値を除した値
を示す。Note 4: Gloss ratio indicates the value obtained by dividing the gloss value after passing through a corrugator machine by the gloss value after pressing.
注5 ・・・・・・ 比較例1.2.4に関しては、表
面にキズが発生しており、光
沢測定が実施出来なかった。Note 5 Regarding Comparative Examples 1.2.4, scratches occurred on the surface and gloss measurement could not be performed.
く効果〉
以上、実施例で示した通り、本発明に係るプレス加工用
被覆剤組成物は、段ボール製造のためのコルゲートマシ
ーンでの貼合工程を通過しても、れが発生せず、高い光
沢を有する段ボール製造等に適した組成物であることが
わかる。Effects> As shown in the Examples above, the coating composition for press processing according to the present invention does not cause any peeling and has a high It can be seen that the composition is suitable for producing glossy corrugated board.
一方、従来のプレス加工用の被覆剤では、−コルゲータ
−適性がなく、段ボール製造には不適なものであること
がわかる。On the other hand, it can be seen that conventional press working coatings are not suitable for corrugators and are unsuitable for corrugated board manufacturing.
なお、本発明に係るプレス加工用被覆剤を使用した段ボ
ールは、光沢付与以外に耐水性あるいは段ボールの強度
向上にも効果的なものである。Note that the corrugated board using the coating material for press processing according to the present invention is effective not only for imparting gloss but also for improving water resistance and strength of the corrugated board.
出願人 サカタインクス株式会社Applicant: Sakata Inx Co., Ltd.
Claims (4)
性樹脂分散物及び無機充填剤を主成分とするプレス加工
用被覆剤組成物。(1) A coating composition for press processing whose main components are an aqueous resin dispersion and an inorganic filler having a glass transition temperature in the range of 60 to 130°C.
有せしめた特許請求の範囲第1項記載のプレス加工用被
覆剤組成物。(2) The coating composition for press working according to claim 1, which contains an inorganic filler in an amount of 0.1 to 5.0% by weight.
スチレン系ビニルモノマーから選ばれたビニルモノマー
を主たる成分とし、乳化重合により得られた水性樹脂分
散物である特許請求の範囲第1項記載のプレス加工用被
覆剤組成物。(3) The aqueous resin dispersion contains an acrylic vinyl monomer,
The coating composition for press processing according to claim 1, which is an aqueous resin dispersion obtained by emulsion polymerization, which contains a vinyl monomer selected from styrenic vinyl monomers as a main component.
チレンアクリル樹脂を乳化剤として用い、アクリル系ビ
ニルモノマー、スチレン系ビニルモノマーから選ばれた
ビニルモノマーを主たる成分とし、乳化重合により得ら
れた水性樹脂分散物である特許請求の範囲第3項記載の
プレス加工用被覆剤組成物。(4) The aqueous resin dispersion is an aqueous resin dispersion obtained by emulsion polymerization using a water-soluble acrylic resin or a water-soluble styrene-acrylic resin as an emulsifier and containing a vinyl monomer selected from acrylic vinyl monomers and styrene-based vinyl monomers as the main component. The coating composition for press processing according to claim 3, which is a resin dispersion.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62253048A JP2562037B2 (en) | 1987-10-07 | 1987-10-07 | Coating composition for press working |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62253048A JP2562037B2 (en) | 1987-10-07 | 1987-10-07 | Coating composition for press working |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0197298A true JPH0197298A (en) | 1989-04-14 |
JP2562037B2 JP2562037B2 (en) | 1996-12-11 |
Family
ID=17245757
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62253048A Expired - Lifetime JP2562037B2 (en) | 1987-10-07 | 1987-10-07 | Coating composition for press working |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2562037B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0525796A (en) * | 1990-09-28 | 1993-02-02 | Tokai Pulp Kk | Readily disaggregating, moisture-proof and water-proof paper and production thereof |
US5441140A (en) * | 1993-08-11 | 1995-08-15 | Escalator Advertising Limited | Escalators |
KR100872538B1 (en) * | 2000-11-30 | 2008-12-08 | 파나소닉 주식회사 | Vector quantizing device for lpc parameters |
WO2018143623A1 (en) * | 2017-02-01 | 2018-08-09 | 한화케미칼 주식회사 | Emulsion and preparing method therefor |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5446911A (en) * | 1977-09-19 | 1979-04-13 | Mitsubishi Paper Mills Ltd | Production of high gloss coated paper |
JPS56140198A (en) * | 1980-04-04 | 1981-11-02 | Daicel Ltd | Paper polishing method |
-
1987
- 1987-10-07 JP JP62253048A patent/JP2562037B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5446911A (en) * | 1977-09-19 | 1979-04-13 | Mitsubishi Paper Mills Ltd | Production of high gloss coated paper |
JPS56140198A (en) * | 1980-04-04 | 1981-11-02 | Daicel Ltd | Paper polishing method |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0525796A (en) * | 1990-09-28 | 1993-02-02 | Tokai Pulp Kk | Readily disaggregating, moisture-proof and water-proof paper and production thereof |
US5441140A (en) * | 1993-08-11 | 1995-08-15 | Escalator Advertising Limited | Escalators |
KR100872538B1 (en) * | 2000-11-30 | 2008-12-08 | 파나소닉 주식회사 | Vector quantizing device for lpc parameters |
WO2018143623A1 (en) * | 2017-02-01 | 2018-08-09 | 한화케미칼 주식회사 | Emulsion and preparing method therefor |
US10954370B2 (en) | 2017-02-01 | 2021-03-23 | Hanwha Chemical Corporation | Emulsion and preparing method therefor |
Also Published As
Publication number | Publication date |
---|---|
JP2562037B2 (en) | 1996-12-11 |
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