JP2000226791A - Coated paper - Google Patents
Coated paperInfo
- Publication number
- JP2000226791A JP2000226791A JP11024171A JP2417199A JP2000226791A JP 2000226791 A JP2000226791 A JP 2000226791A JP 11024171 A JP11024171 A JP 11024171A JP 2417199 A JP2417199 A JP 2417199A JP 2000226791 A JP2000226791 A JP 2000226791A
- Authority
- JP
- Japan
- Prior art keywords
- paper
- parts
- coated paper
- pigment
- weight
- 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.)
- Pending
Links
- 239000011247 coating layer Substances 0.000 claims abstract description 36
- 230000035699 permeability Effects 0.000 claims abstract description 34
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000000049 pigment Substances 0.000 claims abstract description 28
- 239000005995 Aluminium silicate Substances 0.000 claims abstract description 27
- 235000012211 aluminium silicate Nutrition 0.000 claims abstract description 27
- 239000002245 particle Substances 0.000 claims abstract description 24
- 239000012860 organic pigment Substances 0.000 claims abstract description 17
- 239000000853 adhesive Substances 0.000 claims abstract description 9
- 230000001070 adhesive effect Effects 0.000 claims abstract description 9
- 239000000463 material Substances 0.000 claims abstract description 8
- 238000007645 offset printing Methods 0.000 abstract description 4
- 229920005989 resin Polymers 0.000 description 23
- 239000011347 resin Substances 0.000 description 23
- 239000000758 substrate Substances 0.000 description 23
- 238000007639 printing Methods 0.000 description 21
- 238000000576 coating method Methods 0.000 description 20
- 239000011248 coating agent Substances 0.000 description 19
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 16
- 238000000034 method Methods 0.000 description 14
- 238000011156 evaluation Methods 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 10
- 239000010410 layer Substances 0.000 description 10
- 229920002401 polyacrylamide Polymers 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- -1 amine compound Chemical class 0.000 description 8
- 229910000019 calcium carbonate Inorganic materials 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 238000009499 grossing Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 229920000877 Melamine resin Polymers 0.000 description 5
- 229920002472 Starch Polymers 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 235000019698 starch Nutrition 0.000 description 5
- 239000004925 Acrylic resin Substances 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 229920001131 Pulp (paper) Polymers 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000003623 enhancer Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 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 3
- 229920001807 Urea-formaldehyde Polymers 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 3
- 239000001095 magnesium carbonate Substances 0.000 description 3
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 3
- 229920005990 polystyrene resin Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- 239000004368 Modified starch Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 230000009172 bursting Effects 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229920006026 co-polymeric resin Polymers 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000001254 oxidized starch Substances 0.000 description 2
- 235000013808 oxidized starch Nutrition 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229910021647 smectite Inorganic materials 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- XDRLAGOBLZATBG-UHFFFAOYSA-N 1-phenylpenta-1,4-dien-3-one Chemical compound C=CC(=O)C=CC1=CC=CC=C1 XDRLAGOBLZATBG-UHFFFAOYSA-N 0.000 description 1
- 102100031260 Acyl-coenzyme A thioesterase THEM4 Human genes 0.000 description 1
- 102100022704 Amyloid-beta precursor protein Human genes 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 101000638510 Homo sapiens Acyl-coenzyme A thioesterase THEM4 Proteins 0.000 description 1
- 101000823051 Homo sapiens Amyloid-beta precursor protein Proteins 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 229920001407 Modal (textile) Polymers 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- HZVVJJIYJKGMFL-UHFFFAOYSA-N almasilate Chemical compound O.[Mg+2].[Al+3].[Al+3].O[Si](O)=O.O[Si](O)=O HZVVJJIYJKGMFL-UHFFFAOYSA-N 0.000 description 1
- DZHSAHHDTRWUTF-SIQRNXPUSA-N amyloid-beta polypeptide 42 Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O)[C@@H](C)CC)C(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)C1=CC=CC=C1 DZHSAHHDTRWUTF-SIQRNXPUSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- KLIYQWXIWMRMGR-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate Chemical compound C=CC=C.COC(=O)C(C)=C KLIYQWXIWMRMGR-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose 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
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 239000003205 fragrance 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
- 239000003365 glass fiber Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000005389 magnetism Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000013055 pulp slurry Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 229940001941 soy protein Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Thermal Transfer Or Thermal Recording In General (AREA)
- Paper (AREA)
Abstract
(57)【要約】
【課題】 白紙の光沢度が高く、かつオフセット印刷に
おけるインクの受理性に優れ、ブリスタの発生がなく、
高品位な画像が得られる塗工紙を提供する。
【解決手段】 紙基材と、その両面に、顔料と接着剤を
主成分とする塗被層とを設けてなり、前記塗被層中の顔
料100重量部中に、アスペクト比5〜15、平均粒子
径0.3〜1.0μmのカオリンを60重量部以上含
み、かつ前記塗工紙の、塗被層表面の白紙光沢度が50
〜80%、透気度が7000秒以下およびJ.TAPP
I No.54−93に準じる内部結合強さが0.27
〜0.85KJ/m2であることを特徴とするものであ
る。また前記顔料100重量部中に、平均粒子径0.5
〜1.5μmの中空有機顔料を1〜10重量部含むこと
が好ましい。さらに前記紙基材のベック平滑度が50秒
以下、かつ透気度が40秒以下であることが好ましい。(57) [Summary] [Problem] To achieve high glossiness of blank paper, excellent ink receptivity in offset printing, no blistering,
Provide a coated paper from which a high-quality image can be obtained. SOLUTION: A paper base material and a coating layer mainly composed of a pigment and an adhesive are provided on both surfaces thereof, and 100 parts by weight of the pigment in the coating layer have an aspect ratio of 5 to 15, The coated paper contains 60 parts by weight or more of kaolin having an average particle diameter of 0.3 to 1.0 μm, and the coated paper has a white paper glossiness of 50 on the surface of the coating layer.
~ 80%, air permeability of 7000 seconds or less; TAPP
I No. 0.27 internal bond strength according to 54-93
0.80.85 KJ / m 2 . Further, in 100 parts by weight of the pigment, an average particle size of 0.5
It is preferable to include 1 to 10 parts by weight of a hollow organic pigment having a size of 1.5 μm. Further, the paper base material preferably has a Beck smoothness of 50 seconds or less and an air permeability of 40 seconds or less.
Description
【0001】[0001]
【発明の属する技術分野】 本発明は、印刷インクの受
理性に優れ、特に白紙の光沢が高く、ブリスターの発生
しない塗工紙に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a coated paper which is excellent in the receptivity of a printing ink, in particular, has high gloss of a white paper and does not generate blisters.
【0002】[0002]
【従来の技術】 オフセット印刷に用いられる印刷用紙
では、表面が平滑であり、印刷後の刷り上がり感を満足
させるために、紙基体に顔料と接着剤を主成分とする塗
被層を設けたアート紙、コート紙等の塗工紙が使用され
ている。この様な塗工紙は、白紙の光沢度によって低光
沢度からマット(光沢度20%以下)、ダル(光沢度2
0〜45%)、グロス(光沢度45%以上)の3種類に
分けられる。特に白紙光沢の高いグロスは、塗被層を塗
工後、スーパーキャレンダー処理するため、基紙並びに
塗被層の密度が高くなり、透気性(一般塗工紙では、透
気度15000秒程度)が著しく低下するのが特徴であ
る。しかし、インクの乾燥をオーブン等の高熱によって
瞬時に行う輪転方式では、グロスタイプの塗工紙を用い
た場合、インクの乾燥時に画像部のふくれ(以下、ブリ
スタという。)が発生するため、外観が著しく低下する
ことから、改良が望まれている。2. Description of the Related Art In a printing paper used for offset printing, an art in which a coating layer mainly composed of a pigment and an adhesive is provided on a paper base in order to satisfy a finished print after printing is obtained. Coated paper such as paper and coated paper is used. Such a coated paper has a low glossiness to a mat (glossiness of 20% or less), dull (glossiness 2
0-45%) and gloss (gloss 45% or more). In particular, gloss with high glossiness of white paper is subjected to super calendering after coating the coating layer, so that the density of the base paper and the coating layer increases, and the air permeability (in general coated paper, the air permeability is about 15,000 seconds) ) Is markedly reduced. However, in the rotary printing method in which the drying of the ink is instantaneously performed by the high heat of an oven or the like, when a gloss-type coated paper is used, the image portion swells (hereinafter, referred to as a blister) when the ink is dried, so that the appearance is reduced. Therefore, an improvement is desired because of a significant decrease in the value.
【0003】ブリスタについては、インクの熱処理に、
(1)塗工紙中の水蒸気が膨張し、紙基体層が破壊され
て画像部に大きなふくれ、すなわちマクロブリスタが発
生する場合と、(2)インクと塗被層の間の水蒸気が膨
張し、画像部に細かなふくれ、すなわちミクロブリスタ
が発生する場合がある。[0003] Blisters are used for heat treatment of ink.
(1) When the water vapor in the coated paper expands, the paper base layer is broken and large blisters, that is, macro blisters are generated in the image area. (2) The water vapor between the ink and the coating layer expands. In some cases, fine blisters, that is, micro blisters are generated in the image portion.
【0004】一般的な対策として、マクロブリスタにつ
いては、紙基体の内部結合強度を上げ、紙基体層の破裂
を防ぐ方法、またミクロブリスタについては、塗被層の
透気性を向上させる等が考えられる。マクロブリスタに
ついては、特開平3−227491号公報で、ポリアク
リルアミド系の紙力増強剤を添加する方法が提案されて
いるが、添加量を多くすると、フロックが発生するた
め、操業性の面並びに地合の面から添加量は制限され、
得られた紙基体を用いて塗被層を設けても、ブリスタの
改善は十分なされていない。ミクロブリスタについて
は、特開平4−241199号公報で、下塗り層をカチ
オン化することで、下塗り層の空隙率を高め、透気性を
向上させる試みが提案されているが、十分な透気性が得
られていないため、ミクロブリスタを完全には抑えるこ
とが出来ない。[0004] As a general countermeasure, for the macro blister, a method of increasing the internal bonding strength of the paper base to prevent the paper base layer from bursting, and for the micro blister, improving the air permeability of the coating layer are considered. Can be Regarding macro blisters, Japanese Patent Application Laid-Open No. Hei 3-227491 proposes a method of adding a polyacrylamide-based paper-strengthening agent. However, when the amount of addition is increased, floc is generated. The amount of addition is limited in terms of formation,
Even if a coating layer is provided using the obtained paper substrate, the blister has not been sufficiently improved. Regarding micro blisters, Japanese Patent Application Laid-Open No. 4-241199 proposes an attempt to increase the porosity of the undercoat layer by cationizing the undercoat layer and improve the air permeability, but sufficient air permeability is obtained. Therefore, micro-blisters cannot be completely suppressed.
【0005】[0005]
【発明が解決しようとする課題】 本発明は、上記の問
題点を改善することを目的とするものであって、白紙の
光沢度が高く、かつオフセット印刷におけるインクの受
理性に優れ、ブリスタの発生がなく、高品位な画像が得
られる塗工紙を提供するものである。SUMMARY OF THE INVENTION An object of the present invention is to improve the above-described problems, and it is intended to improve the glossiness of blank paper and the ink receptivity in offset printing. An object of the present invention is to provide a coated paper from which high quality images can be obtained without generation.
【0006】[0006]
【課題を解決するための手段】 本発明者らは上記の目
的を達成するため、紙基体の内部結合強さと塗被層の透
気性との関係と、ブリスタの発生について、鋭意研究し
た結果、紙基材の両面に顔料と接着剤を主成分とする塗
被層を設けてなる塗工紙において、厚みに対する平面長
径の比であるアスペクト比および平均粒子径が特定の範
囲であるカオリンを主顔料とした塗被液を塗工、乾燥
し、平滑化処理し、そこで得た塗工紙が、透気性を有
し、特定の範囲の内部結合強さを有するものであること
を見出し、本発明を完成させたものである。Means for Solving the Problems In order to achieve the above object, the present inventors have conducted intensive studies on the relationship between the internal bond strength of a paper substrate and the air permeability of a coating layer, and on the occurrence of blisters. In a coated paper in which a coating layer mainly composed of a pigment and an adhesive is provided on both sides of a paper base material, kaolin having a specific range of an aspect ratio and an average particle size, which are a ratio of a plane major axis to a thickness, is mainly used. The coating liquid as a pigment was coated, dried and smoothed, and the coated paper obtained was found to have air permeability and a specific range of internal bond strength. The invention has been completed.
【0007】すなわち本発明に係る塗工紙は、紙基材
と、その両面に、顔料と接着剤を主成分とする塗被層と
を設けてなり、前記塗被層中の顔料100重量部中に、
アスペクト比5〜15、平均粒子径0.3〜1.0μm
のカオリンを60重量部以上含み、かつ前記塗工紙の、
塗被層表面の白紙光沢度が50〜80%、透気度が70
00秒以下およびJ.TAPPI No.54−93に
準じる内部結合強さが0.27〜0.85KJ/m2で
あることを特徴とするものである。That is, the coated paper according to the present invention comprises a paper base material and, on both sides thereof, a coating layer mainly composed of a pigment and an adhesive, and 100 parts by weight of the pigment in the coating layer. inside,
Aspect ratio 5-15, average particle size 0.3-1.0 μm
Containing at least 60 parts by weight of kaolin, and of the coated paper,
The glossiness of blank paper on the surface of the coating layer is 50 to 80%, and the air permeability is 70.
00 seconds or less; TAPPI No. Internal bond strength analogous to 54-93 is characterized in that a 0.27~0.85KJ / m 2.
【0008】また前記顔料100重量部中に、平均粒子
径0.5〜1.5μmの中空有機顔料を1〜10重量部
含むことが好ましい。さらに前記紙基材のベック平滑度
が50秒以下、かつ透気度が40秒以下であることが好
ましい。It is preferable that 100 parts by weight of the pigment contains 1 to 10 parts by weight of a hollow organic pigment having an average particle size of 0.5 to 1.5 μm. Further, the paper base material preferably has a Beck smoothness of 50 seconds or less and an air permeability of 40 seconds or less.
【0009】[0009]
【発明の実施の形態】 本発明者等は、塗工紙に高光沢
度と低透気度を付与することについて、軽度の平滑化処
理により塗被層を嵩高な構造に保ちながら高光沢を得る
必要があると考え、鋭意研究を重ねた結果、塗被層の主
顔料に、アスペクト比が5〜15の範囲にあり、かつ平
均粒子径が0.3〜1.0μmであるカオリンを用いる
ことで、高光沢と高透気性が得られることを見出し、マ
クロブリスタおよびミクロブリスタの発生が生じない塗
工紙を得た。BEST MODE FOR CARRYING OUT THE INVENTION The present inventors have proposed that high gloss and low air permeability can be imparted to coated paper while maintaining a high gloss while maintaining a coated layer in a bulky structure by a light smoothing treatment. As a result of intensive studies, it is necessary to obtain kaolin having an aspect ratio in the range of 5 to 15 and an average particle diameter of 0.3 to 1.0 μm as the main pigment of the coating layer. As a result, it has been found that high gloss and high air permeability can be obtained, and coated paper free of generation of macro blisters and micro blisters has been obtained.
【0010】一般に用いられているアスペクト比15〜
20のカオリンや、アスペクト比40以上のデラミネー
トカオリンと比較し、本発明で用いるカオリンは、アス
ペクト比が5〜15の範囲にあり、厚みの大きな形状
で、かつ平均粒子径が0.3〜1.0μmと小さく、粒
度分布が均一な六角板状であるため、塗被層が平滑化処
理された後、顔料間の間隙が密な構造とならず、かつ六
角板状カオリンの特徴である高い平面性を備えているか
らであると推測される。[0010] Generally used aspect ratio of 15 to
Compared to kaolin 20 or delaminated kaolin having an aspect ratio of 40 or more, the kaolin used in the present invention has an aspect ratio in the range of 5 to 15, has a large thickness, and has an average particle diameter of 0.3 to 0.3. Since it is a small hexagonal plate with a small particle size of 1.0 μm and a uniform particle size distribution, the gap between the pigments does not become a dense structure after the coating layer is smoothed, and it is a characteristic of hexagonal plate-shaped kaolin. It is presumed that this is because it has high flatness.
【0011】ちなみに粒子径が0.3μmより小さい場
合、光沢は出やすくなるが、透気性が著しく低下する。
一方、1.0μmを越えて大きくなると、光沢が出にく
くなり、所望の光沢を得ることが出来ない。また粒度分
布についても、粒子径0.25〜1.0μmの粒度分布
が65%以上であることが好ましい。When the particle size is smaller than 0.3 μm, gloss tends to be obtained, but air permeability is significantly reduced.
On the other hand, if it is larger than 1.0 μm, it becomes difficult to obtain gloss, and a desired gloss cannot be obtained. Regarding the particle size distribution, it is preferable that the particle size distribution with a particle size of 0.25 to 1.0 μm is 65% or more.
【0012】本発明の主顔料として用いるカオリンは、
塗被層中の全顔料100重量部に対し、60重量部〜1
00重量部の範囲で配合される。ちなみに、60重量部
未満では、透気性が著しく低下する。Kaolin used as the main pigment of the present invention is
60 parts by weight to 1 part by weight based on 100 parts by weight of all pigments in the coating layer
It is blended in the range of 00 parts by weight. By the way, if it is less than 60 parts by weight, the air permeability is significantly reduced.
【0013】さらに本発明者らは、マクロブリスタの発
生を抑えることについて鋭意研究を重ねた結果、J.T
APPI No.54−93に準じる内部結合強さが
0.27〜0.85KJ/m2に調整することで、紙基
体の層間の破裂によって発生するマクロブリスタを防止
することが可能であることを突き止めた。ちなみに、内
部結合強さが0.27KJ/m2未満では、塗工紙の透
気性を高めても、マクロブリスタの発生を完全に防止出
来ない。一方、0.85KJ/m2を越える場合、パル
プフロックが発生し、地合、外観が著しく低下する。好
ましくは、0.35〜0.85KJ/m2である。Further, the present inventors have conducted intensive studies on suppressing the generation of macro blisters. T
APPI No. It has been found that by adjusting the internal bond strength according to No. 54-93 to 0.27 to 0.85 KJ / m 2 , it is possible to prevent macro blisters generated by bursting between layers of the paper substrate. Incidentally, when the internal bond strength is less than 0.27 KJ / m 2 , the generation of macro blisters cannot be completely prevented even if the air permeability of the coated paper is increased. On the other hand, when it exceeds 0.85 KJ / m 2 , pulp flocs are generated, and the formation and appearance are significantly reduced. Preferably, a 0.35~0.85KJ / m 2.
【0014】紙基体の内部結合強さの向上に対しては、
例えば、剛性の高い針葉樹から製造されたようなパルプ
の種類、叩解を進めて繊維間結合を高めること、紙力増
強剤の添加、樹脂の含浸、塗工などがあるが、目的に応
じて適宜選択される。To improve the internal bond strength of the paper substrate,
For example, there are types of pulp such as those manufactured from high-rigidity softwood, improving the inter-fiber bonding by advancing beating, addition of a paper strength enhancer, resin impregnation, coating, etc., but depending on the purpose, Selected.
【0015】本発明の紙基体は、ベック平滑度が50秒
以下、透気度が40秒以下であることが望ましい。ベッ
ク平滑度が50秒を越えると、ストリークの発生や、塗
料の付着が悪くなるなど操業性が低下することがある。
また透気度が40秒を越えると、塗被層を設け、平滑化
処理を施した後の透気性が悪くなり、ブリスタの発生を
完全に防止出来ない。好ましくは、ベック平滑度が30
秒以下、透気度が30秒以下である。The paper substrate of the present invention preferably has a Beck smoothness of 50 seconds or less and an air permeability of 40 seconds or less. If the Bekk smoothness exceeds 50 seconds, operability may be reduced, such as occurrence of streaks and poor adhesion of paint.
On the other hand, if the air permeability exceeds 40 seconds, the air permeability after providing the coating layer and performing the smoothing treatment becomes poor, and the generation of blisters cannot be completely prevented. Preferably, the Beck smoothness is 30
Seconds or less, air permeability is 30 seconds or less.
【0016】紙基体のベック平滑度の調整は、マシンキ
ャレンダー、ソフトニップキャレンダー等の平滑化処理
装置を用いて行われる。一方、透気度の調整は、ポリア
ミド、アクリルアミド、アミン化合物、アミド、エポキ
シやメラミン系化合物等の紙力増強剤、天然ワックス、
オレフィン系、ジルコニウム系またはフッ素系ワックス
の撥水剤、およびポリビニルアルコール、フッ素系樹
脂、アクリル系樹脂、スチレン系樹脂、アクリル−スチ
レン系共重合体樹脂、アミド系樹脂、ウレタン系樹脂、
エポキシ系樹脂等の水溶性樹脂あるいは水分散性樹脂を
含浸、サイズプレス塗工などの処理で行われる。The Beck smoothness of the paper substrate is adjusted using a smoothing device such as a machine calender or a soft nip calender. On the other hand, the adjustment of the air permeability is made of a paper-strength enhancer such as polyamide, acrylamide, amine compound, amide, epoxy or melamine compound, natural wax,
Olefin-based, zirconium-based or fluorine-based wax water repellent, and polyvinyl alcohol, fluorine-based resin, acrylic resin, styrene-based resin, acryl-styrene-based copolymer resin, amide-based resin, urethane-based resin,
It is performed by a process such as impregnation with a water-soluble resin such as an epoxy resin or a water-dispersible resin, and size press coating.
【0017】本発明では、塗被層中に平均粒子径0.5
〜1.5μmの中空有機顔料を全顔料重量に対して、1
〜10重量部配合されることも可能である。In the present invention, the coating layer has an average particle size of 0.5
To 1.5 μm hollow organic pigment,
It is also possible to mix up to 10 parts by weight.
【0018】本発明者らは、印刷インクの受理性を向上
させることについて鋭意研究を重ねた結果、塗被層中に
平均粒子径0.5〜1.5μmの中空有機顔料を全顔料
100重量部に対して、1〜10重量部配合すると、印
刷インクの受理性が向上することを見出し、本発明を完
成するに至った。この現象については、明確ではない
が、塗被層中に柔らかく、クッション性の高い中空有機
顔料が配合されることで、塗被層表面のクッション性が
向上したことと、中空有機顔料とインクとの親和性が良
いことが推定される。The present inventors have conducted intensive studies on improving the receptivity of the printing ink. As a result, 100% by weight of the hollow organic pigment having an average particle diameter of 0.5 to 1.5 μm was added to the coating layer. It was found that the addition of 1 to 10 parts by weight with respect to parts improved the acceptability of the printing ink, and the present invention was completed. About this phenomenon, it is not clear, but by mixing a soft, high cushioning hollow organic pigment in the coating layer, the cushioning property of the coating layer surface has been improved, and the hollow organic pigment and ink Is presumed to have good affinity.
【0019】ちなみに、中空有機顔料の平均粒子径が
0.5μm未満では、塗被層の透気性が低下することが
ある。一方、その平均粒子径が1.5μmより大きくな
ると、所望の光沢が得られないことがある。また配合量
が10重量部を越えると、ストリーク等の操業性が著し
く低下することがある。また中空有機顔料の配合量が1
0重量部を越えると、塗被層の強度が低下し、印刷時
に、ブランケットの汚れを発生させることがある。より
好ましい配合量は1〜4重量部である。If the average particle size of the hollow organic pigment is less than 0.5 μm, the air permeability of the coating layer may be reduced. On the other hand, if the average particle size is larger than 1.5 μm, desired gloss may not be obtained. When the amount exceeds 10 parts by weight, operability such as streak may be remarkably reduced. When the amount of the hollow organic pigment is 1
If the amount is more than 0 parts by weight, the strength of the coating layer is reduced, and the blanket may be stained during printing. A more preferred amount is 1 to 4 parts by weight.
【0020】本発明で用いられる中空有機顔料は、ポリ
スチレン系樹脂、スチレン−アクリル共重合体系樹脂、
尿素系樹脂、メラミン系樹脂、アクリル系樹脂、塩化ビ
ニリデン系樹脂、ベンゾグアナミン系樹脂が挙げられ、
これらの中から1種あるいは2種以上が適宜選択して用
いられる。The hollow organic pigment used in the present invention may be a polystyrene resin, a styrene-acrylic copolymer resin,
Urea resin, melamine resin, acrylic resin, vinylidene chloride resin, benzoguanamine resin,
One or more of these are appropriately selected and used.
【0021】紙基体のパルプについては、製法や種類等
について、特に限定するものではなく、KPのような化
学パルプ、SGP、RGP、BCTMP、CTMP等の
機械パルプや、脱墨パルプのような古紙パルプ、あるい
はケフナ、竹、藁、麻等のような非木材パルプ、ポリア
ミド繊維、ポリエステル繊維、ポリノジック繊維等の有
機合成繊維、さらにはガラス繊維、セラミック繊維、カ
ーボン繊維等の無機質繊維も使用出来る。The pulp of the paper substrate is not particularly limited with respect to the production method and the kind, etc., and chemical pulp such as KP, mechanical pulp such as SGP, RGP, BCTMP and CTMP, and used paper such as deinked pulp Pulp, non-wood pulp such as kefna, bamboo, straw, hemp, and the like, organic synthetic fibers such as polyamide fiber, polyester fiber, and polynosic fiber, and inorganic fibers such as glass fiber, ceramic fiber, and carbon fiber can also be used.
【0022】また紙基体中には、必要に応じて、填料が
配合出来る。この場合の填料としては、特に限定するも
のではないが、一般に上質紙に用いられる各種の顔料、
例えばカオリン、焼成カオリン、炭酸カルシウム、硫酸
カルシウム、硫酸バリウム、二酸化チタン、タルク、酸
化亜鉛、アルミナ、炭酸マグネシウム、酸化マグネシウ
ム、シリカ、ホワイトカーボン、ベントナイト、ゼオラ
イト、セリサイト、スメクタイト等の鉱物質顔料や、ポ
リスチレン系樹脂、尿素系樹脂、メラミン系樹脂、アク
リル系樹脂、塩化ビニリデン系樹脂並びにそれらの微小
中空粒子等の有機顔料が挙げられる。A filler can be added to the paper substrate as needed. The filler in this case is not particularly limited, but various pigments generally used for high quality paper,
For example, mineral pigments such as kaolin, calcined kaolin, calcium carbonate, calcium sulfate, barium sulfate, titanium dioxide, talc, zinc oxide, alumina, magnesium carbonate, magnesium oxide, silica, white carbon, bentonite, zeolite, sericite, smectite and the like. And organic pigments such as polystyrene resins, urea resins, melamine resins, acrylic resins, vinylidene chloride resins, and fine hollow particles thereof.
【0023】なお紙料中にはパルプ繊維や填料の他に、
本発明の所望の効果を損なわない範囲で、従来から使用
されている各種のアニオン性、ノニオン性、カチオン性
あるいは両性の歩留向上剤、濾水性向上剤、紙力増強剤
や内添サイズ剤等の各種抄紙用内添助剤が必要に応じて
適宜選択して使用することができる。さらに染料、蛍光
増白剤、pH調整剤、消泡剤、ピッチコントロール剤、
スライムコントロール剤等の抄紙用内添助剤も紙の用途
に応じて適宜添加することができる。In the paper stock, besides pulp fiber and filler,
Various anionic, nonionic, cationic or amphoteric retention improvers, drainage improvers, paper-strength enhancers and internal sizing agents that have been conventionally used within the range not impairing the desired effects of the present invention. And the like can be appropriately selected and used as needed. Furthermore, dyes, optical brighteners, pH adjusters, defoamers, pitch control agents,
An internal additive for papermaking, such as a slime control agent, can also be appropriately added according to the use of the paper.
【0024】抄紙方法については特に限定するものでは
なく、例えば抄紙pHが4.5付近である酸性抄紙法、
炭酸カルシウム等のアルカリ性填料を主成分として含み
抄紙pH約6の弱酸性から抄紙pH約9の弱アルカリ性
の中性抄紙法等の全ての抄紙方法に適用することがで
き、抄紙機も長網抄紙機、ツインワイヤー抄紙機、丸網
抄紙機、ヤンキー抄紙機を適宜使用することができる。The papermaking method is not particularly limited, and examples thereof include an acidic papermaking method having a papermaking pH of about 4.5,
It can be applied to all papermaking methods, including alkaline filler such as calcium carbonate as a main component, from weakly acidic papermaking pH of about 6 to weakly alkaline neutral papermaking method of papermaking pH of about 9, and the paper machine is also Fourdrinier papermaking. Machine, twin wire paper machine, round mesh paper machine, Yankee paper machine can be used as appropriate.
【0025】本発明の塗工紙に用いる顔料としては、本
発明のカオリンや中空有機顔料のほかに、例えば、重質
炭酸カルシウム、軽質炭酸カルシウム、カオリン、焼成
カオリン、構造性カオリン、デラミカオリン、タルク、
硫酸カルシウム、硫酸バリウム、二酸化チタン、酸化亜
鉛、アルミナ、炭酸マグネシウム、酸化マグネシウム、
シリカ、アルミノ珪酸マグネシウム、微粒子状珪酸カル
シウム、微粒子状炭酸マグネシウム、微粒子状軽質炭酸
カルシウム、ホワイトカーボン、ベントナイト、ゼオラ
イト、セリサイト、スメクタイト等の鉱物質顔料や、ポ
リスチレン系樹脂、スチレン−アクリル共重合体系樹
脂、尿素系樹脂、メラミン系樹脂、アクリル系樹脂、塩
化ビニリデン系樹脂、ベンゾグアナミン系樹脂等の密実
型や貫通孔型樹脂等の有機顔料も用いることが可能であ
り、これらの中から1種あるいは2種以上が適宜選択し
て用いられる。As the pigment used in the coated paper of the present invention, in addition to the kaolin of the present invention and the hollow organic pigment, for example, heavy calcium carbonate, light calcium carbonate, kaolin, calcined kaolin, structural kaolin, delamikaolin, talc,
Calcium sulfate, barium sulfate, titanium dioxide, zinc oxide, alumina, magnesium carbonate, magnesium oxide,
Mineral pigments such as silica, magnesium aluminosilicate, finely divided calcium silicate, finely divided magnesium carbonate, finely divided light calcium carbonate, white carbon, bentonite, zeolite, sericite, smectite, polystyrene resin, styrene-acrylic copolymer Organic pigments such as resin, urea resin, melamine resin, acrylic resin, vinylidene chloride resin, benzoguanamine resin and the like, and organic pigments such as through-hole resin can be used. Alternatively, two or more kinds are appropriately selected and used.
【0026】接着剤としては、水溶性及び/または水分
散性の高分子化合物を用いることが出来、例えば、カチ
オン性澱粉、両性澱粉、酸化澱粉、酵素変性澱粉、熱化
学変性澱粉、エステル化澱粉、エ−テル化澱粉等の澱粉
類、カルボキシメチルセルロース、ヒドロキシエチルセ
ルロース等のセルロース誘導体、ゼラチン、カゼイン、
大豆蛋白、天然ゴム等の天然あるいは半合成高分子化合
物、ポリビニルアルコール、イソプレン、ネオプレン
(登録商標)、ポリブタジエン等のポリジエン類、ポリ
ブテン、ポリイソブチレン、ポリプロピレン、ポリエチ
レン等のポリアルケン類、ビニルハライド、酢酸ビニ
ル、スチレン、(メタ)アクリル酸、(メタ)アクリル
酸エステル、(メタ)アクリルアミド、メチルビニルエ
ーテル等のビニル系重合体や共重合体類、スチレン−ブ
タジエン系、メチルメタクリレート−ブタジエン系等の
合成ゴムラテックス、ポリウレタン系樹脂、ポリエステ
ル系樹脂、ポリアミド系樹脂、オレフィン−無水マレイ
ン酸系樹脂、メラミン系樹脂等の合成高分子化合物等が
例示できる。これらの中から目的に応じて1種あるいは
2種以上が適宜選択して使用される。As the adhesive, a water-soluble and / or water-dispersible polymer compound can be used. For example, cationic starch, amphoteric starch, oxidized starch, enzyme-modified starch, thermochemically modified starch, esterified starch , Starches such as etherified starch, carboxymethyl cellulose, cellulose derivatives such as hydroxyethyl cellulose, gelatin, casein,
Natural or semi-synthetic polymer compounds such as soy protein, natural rubber, etc .; polydienes such as polyvinyl alcohol, isoprene, neoprene (registered trademark) and polybutadiene; polyalkenes such as polybutene, polyisobutylene, polypropylene and polyethylene; vinyl halide; vinyl acetate Vinyl polymers and copolymers such as styrene, styrene, (meth) acrylic acid, (meth) acrylic acid ester, (meth) acrylamide, and methyl vinyl ether; and synthetic rubber latex such as styrene-butadiene and methyl methacrylate-butadiene. And synthetic polymers such as polyurethane resins, polyester resins, polyamide resins, olefin-maleic anhydride resins, and melamine resins. One or more of these may be appropriately selected and used depending on the purpose.
【0027】接着剤の配合割合は、顔料100重量部
(固型分)に対して、5〜50重量部(固型分)の範囲
である。ちなみに5重量部未満では、塗被層の塗膜の強
度が弱く、輪転機の印刷版に塗被層が剥がれ堆積し、印
刷版を傷つける原因となることがある。一方、これが5
0重量部を越えると、塗被層が緻密になり、透気性が著
しく低下することがある。The mixing ratio of the adhesive is in the range of 5 to 50 parts by weight (solid part) based on 100 parts by weight (solid part) of the pigment. If the amount is less than 5 parts by weight, the strength of the coating film of the coating layer is weak, and the coating layer may peel off and accumulate on the printing plate of a rotary press, which may cause damage to the printing plate. On the other hand, this is 5
If the amount exceeds 0 parts by weight, the coating layer becomes dense and the air permeability may be significantly reduced.
【0028】この塗被液中には、これら顔料や接着剤の
他に各種助剤、例えば界面活性剤、pH調節剤、粘度調
節剤、柔軟剤、光沢付与剤、ワックス類、分散剤、流動
変性剤、導電防止剤、安定化剤、帯電防止剤、架橋剤、
サイズ剤、蛍光増白剤、着色剤、紫外線吸収剤、消泡
剤、耐水化剤、可塑剤、滑剤、防腐剤、香料等が必要に
応じて適宜使用することも可能である。In the coating liquid, in addition to these pigments and adhesives, various auxiliaries such as surfactants, pH adjusters, viscosity adjusters, softeners, gloss imparting agents, waxes, dispersants, fluidizers Denaturing agents, antistatic agents, stabilizers, antistatic agents, crosslinking agents,
A sizing agent, a fluorescent whitening agent, a coloring agent, an ultraviolet absorber, an antifoaming agent, a waterproofing agent, a plasticizer, a lubricant, a preservative, a fragrance, and the like can be appropriately used as needed.
【0029】本発明の塗被層の塗工量は、8〜20g/
m2、好ましくは10〜20g/m2が必要である。塗工
量が8g/m2未満では、紙基体表面の凹凸を十分に覆
うことが出来ないため、印刷インクの受理性が著しく低
下することがある。一方、20g/m2を越えると、塗
工時の乾燥性が悪くなるなどの操業性が低下し、製造原
価も高くなる。The coating amount of the coating layer of the present invention is 8 to 20 g /
m 2 , preferably 10 to 20 g / m 2 is required. If the coating amount is less than 8 g / m 2 , it is not possible to sufficiently cover the irregularities on the surface of the paper substrate, so that the acceptability of the printing ink may be significantly reduced. On the other hand, if it exceeds 20 g / m 2 , operability such as poor drying property during coating is reduced, and the production cost is increased.
【0030】塗被層を形成する塗被方法としては、一般
に公知の塗被装置、例えばブレードコータ、エヤーナイ
フコータ、ロールコータ、リバースロールコータ、バー
コータ、カーテンコータ、ダイスロットコータ、グラビ
アコータ、チャンプレックスコータ、ブラシコータ、ツ
ーロールあるいはメータリングブレード式のサイズプレ
スコータ、ビルブレードコータ、ショートドウェルコー
タ、ゲートロールコータ等の装置が適宜用いられる。As a coating method for forming a coating layer, generally known coating apparatuses such as a blade coater, an air knife coater, a roll coater, a reverse roll coater, a bar coater, a curtain coater, a die slot coater, a gravure coater, and a chanter Apparatuses such as a plex coater, a brush coater, a two-roll or metering blade type size press coater, a bill blade coater, a short dwell coater, and a gate roll coater are appropriately used.
【0031】塗被層は、紙基体の両面に形成され、必要
に応じ、1層あるいは必要に応じて2層以上の中間層を
設け、多層構造にすることも可能である。なお両面塗工
や多層構造にする場合、各々の塗被液が同一または同一
塗工量である必要はなく、所要の品質レベルに応じて適
宜調整して配合すればよく、特に限定されるものではな
い。また紙基体の片面に塗被層を設けた場合、裏面に合
成樹脂層、顔料と接着剤等からなる塗被層や、帯電防止
層等を設けてカール防止、印刷適性付与、給排紙適性等
を付与することも可能である。さらに紙基体の裏面に種
々の加工、例えば粘着、磁性、難燃、耐熱、耐水、耐
油、防滑等の後加工を施すことにより、用途適性を付加
して使用することも勿論可能である。The coating layer is formed on both sides of the paper substrate, and if necessary, one layer or two or more intermediate layers may be provided to form a multilayer structure. In the case of a double-sided coating or a multilayer structure, each coating liquid does not need to have the same or the same coating amount, and may be appropriately adjusted and blended according to a required quality level, and is particularly limited. is not. When a coating layer is provided on one side of the paper substrate, a coating layer made of a synthetic resin layer, a pigment and an adhesive, or an antistatic layer is provided on the back side to prevent curling, impart printability, and supply and discharge paper. It is also possible to give the like. Further, the back surface of the paper substrate may be subjected to various processes, for example, post-processes such as adhesion, magnetism, flame retardancy, heat resistance, water resistance, oil resistance, and anti-slipping, so that it is possible to use the paper substrate with additional applicability.
【0032】本発明は、紙基体上に塗被層を設けた後、
通常の乾燥工程や表面処理工程等で平滑化処理されて、
水分が3〜10%、好ましくは4〜8%程度となるよう
に調整して仕上げられる。According to the present invention, after providing a coating layer on a paper substrate,
It is smoothed in a normal drying process or surface treatment process, etc.
It is finished by adjusting the water content to be about 3 to 10%, preferably about 4 to 8%.
【0033】また平滑化処理する際は、通常のスーパー
キャレンダ、グロスキャレンダ、ソフトキャレンダ等の
平滑化処理装置で行われ、オンマシンやオフマシンで適
宜用いられ、加圧装置の形態、加圧ニップの数、加温等
も通常の平滑化処理装置に準じて適宜調節される。The smoothing process is performed by a normal smoothing device such as a super calender, a gloss calender, a soft calender, etc., and is used as appropriate in an on-machine or an off-machine. The number of pressure nips, heating, and the like are also appropriately adjusted according to a normal smoothing treatment device.
【0034】平滑化処理を施した塗工紙は、印刷用紙の
風合いを備えることが必要となるため、JIS Z87
41に基づく入射・受光角75度の白紙光沢度は50〜
80%が好ましく、より好ましくは60〜80%であ
る。さらに透気度は7000秒以下に調整されることが
好ましく、より好ましくは5000秒以下、さらに好ま
しくは3000秒以下である。Since the coated paper subjected to the smoothing treatment needs to have the texture of the printing paper, it is required to conform to JIS Z87.
The glossiness of blank paper at 75 degrees of incidence / receiving angle based on 41 is 50 ~
It is preferably 80%, more preferably 60 to 80%. Further, the air permeability is preferably adjusted to 7000 seconds or less, more preferably 5000 seconds or less, and still more preferably 3000 seconds or less.
【0035】光沢度が50%未満では、白紙の外観や所
望のグロス感が得られないことがあり、一方、光沢度を
80%より高くすると、本発明に用いる顔料を使用して
も、透気度を7000秒以下に調整出来ず、マクロブリ
スタまたはミクロブリスタが発生することがある。ちな
みに透気度が7000秒を越えると、塗工紙の内部結合
強度が0.27〜0.85KJ/m2でも、ミクロブリ
スタが発生することがある。一方、透気度が5000秒
以下でも内部結合強度が0.27KJ/m2未満の場
合、マクロブリスタが発生することがある。If the glossiness is less than 50%, the appearance of a white paper and the desired glossiness may not be obtained. On the other hand, if the glossiness is higher than 80%, even if the pigment used in the present invention is used, the transparency will not increase. The temper cannot be adjusted to 7000 seconds or less, and macro blisters or micro blisters may occur. By the way, if the air permeability exceeds 7000 seconds, micro blisters may be generated even if the internal bond strength of the coated paper is 0.27 to 0.85 KJ / m 2 . On the other hand, when the internal bonding strength is less than 0.27 KJ / m 2 even when the air permeability is 5000 seconds or less, macro blisters may be generated.
【0036】上述の方法によって、得られた塗工紙は、
オフセット輪転印刷適性はもとより、表面の高平滑性と
高透気性から、電子写真方式や熱転写方式等のノンイン
パクトプリンティング方式の画像記録用紙として用いる
ことも出来る。The coated paper obtained by the above method is
It can be used as a non-impact printing type image recording paper such as an electrophotographic type or a thermal transfer type because of its surface smoothness and high air permeability as well as its offset rotary printing suitability.
【0037】[0037]
【実施例】 以下に、実施例を挙げて本発明をより具体
的に説明するが,勿論、それらの範囲に限定されるもの
でない。なお、例中の「部」及び「%」は特に断わらな
い限り、「重量部(固型分)」及び「重量%」を示す。EXAMPLES Hereinafter, the present invention will be described more specifically with reference to Examples, but it is needless to say that the present invention is not limited to these ranges. In the examples, “parts” and “%” indicate “parts by weight (solid content)” and “% by weight” unless otherwise specified.
【0038】実施例1 〔基材の調製〕LBKP(フリーネス(CSF)=50
0ml)70部、NBKP(フリーネス(CSF)=5
00ml)30部のパルプスラリーに、紙力増強剤とし
てポリアクリルアミド系樹脂(商品名;PS117、荒
川化学工業社製)0.1%と、ポリアクリルアミド系樹
脂(商品名;PS460、荒川化学工業社製)0.3
%、硫酸バンド1部を添加し、これらの混合物を白水で
希釈してpH5.3、固形分濃度1.1%の紙料を調製
した。この紙料を長網抄紙機を用いて抄紙し、次いで、
ポリアクリルアミド系樹脂(商品名;ポリマセット53
1、荒川化学工業社製)の液濃度2%のサイズプレス液
を、塗布量が乾燥重量で1g/m2となるようにサイズ
プレス装置で塗布し、乾燥させ、マシンキャレンダーで
ベック平滑度30秒になるように平滑処理して坪量が8
0g/m2の基紙を得た(紙基体)。紙基体のベック
平滑度、透気度並びに内部結合強さについて、表1に示
す。Example 1 [Preparation of base material] LBKP (freeness (CSF) = 50
0ml) 70 parts, NBKP (freeness (CSF) = 5
(00ml) 30 parts of pulp slurry, 0.1% of polyacrylamide resin (trade name: PS117, manufactured by Arakawa Chemical Industries) as a paper strength enhancer and polyacrylamide resin (trade name: PS460, Arakawa Chemical Co., Ltd.) 0.3)
% And one part of a sulfuric acid band, and the mixture was diluted with white water to prepare a stock having a pH of 5.3 and a solid content of 1.1%. The stock is made using a Fourdrinier machine,
Polyacrylamide resin (trade name; Polymer Set 53)
1, Arakawa Chemical Industry Co., Ltd.) with a size press of 2%, applied by a size press so that the applied amount becomes 1 g / m 2 in dry weight, dried and Beck smoothness by machine calender Smooth processing to 30 seconds to obtain a basis weight of 8
A base paper of 0 g / m 2 was obtained (paper base). Table 1 shows the Beck smoothness, air permeability, and internal bond strength of the paper substrate.
【0039】〔塗被液の調整と塗布〕アストラプラス
(成分;カオリン、ヒューバー社製)100部に、分散
剤としてポリアクリル酸ソーダ(商品名 アロンA−
9、東亜合成社製)を0.2部を加え、コーレス分散機
を用いて水分散して顔料スラリーを調製した。この顔料
スラリーに酸化澱粉(商品名;エースA、王子コーンス
ターチ社製)3.0部、スチレンーブタジエン系共重合
体ラテックス(商品名;OX1060 日本ゼオン社
製)10部を添加、攪拌し、さらに水を加えて、固形分
濃度が50%の塗被液を調製した。用いた無機顔料の組
成、形状、アスペクト比、平均粒子径並びに粒度分布を
表2に示す。[Preparation and Coating of Coating Liquid] 100 parts of Astra Plus (component: Kaolin, manufactured by Huber Corporation) was used as a dispersant with sodium polyacrylate (trade name: Alon A-
9, manufactured by Toa Gosei Co., Ltd.), and dispersed in water using a CORES disperser to prepare a pigment slurry. 3.0 parts of oxidized starch (trade name; Ace A, manufactured by Oji Cornstarch Co., Ltd.) and 10 parts of styrene butadiene copolymer latex (trade name: OX1060, manufactured by Zeon Corporation) are added to the pigment slurry, and the mixture is stirred. Water was added to prepare a coating liquid having a solid content of 50%. Table 2 shows the composition, shape, aspect ratio, average particle size, and particle size distribution of the inorganic pigments used.
【0040】〔紙基体への塗被層の形成〕得られた塗被
液を上記の紙基体の片面当たり乾燥重量で12g/m2
となるようにブレードコータを用いて両面塗被し、金属
ロールと弾性ロールで構成された加圧ニップに通紙し
て、JIS Z8741に基づく入射・受光角75度の
白紙光沢度が65%になるように調整して、坪量が10
4g/m2の塗工紙を得た。[Formation of Coating Layer on Paper Substrate] The obtained coating liquid was dried at a dry weight of 12 g / m 2 per one side of the paper substrate.
Using a blade coater, both sides are coated using a blade coater, and the paper is passed through a pressure nip composed of a metal roll and an elastic roll, and the glossiness of the white paper at an incident / receiving angle of 75 degrees according to JIS Z8741 is 65%. So that the basis weight is 10
4 g / m 2 of coated paper was obtained.
【0041】実施例2 実施例1で使用したアストラプラス(成分;カオリン、
ヒューバー社製)100部を、アストラプラス70部と
ブリリアント(成分;軽質炭酸カルシウム、白石カルシ
ウム社製)30部に変更した以外は同様に塗工紙を作成
し、評価した。Example 2 Astraplus used in Example 1 (components: kaolin,
A coated paper was prepared and evaluated in the same manner, except that 100 parts of Huber Co.) was changed to 70 parts of Astra Plus and 30 parts of Brilliant (component: light calcium carbonate, manufactured by Shiraishi Calcium Co.).
【0042】比較例1 実施例1で使用したアストラプラス(成分;カオリン、
ヒューバー社製)100部を、アストラプラス50部と
ブリリアント(成分;軽質炭酸カルシウム、白石カルシ
ウム社製)50部に変更した以外は同様に塗工紙を作成
し、評価した。Comparative Example 1 Astraplus used in Example 1 (components: kaolin,
A coated paper was prepared and evaluated in the same manner except that 100 parts of HUBER Co., Ltd. was changed to 50 parts of Astra Plus and 50 parts of brilliant (component: light calcium carbonate, manufactured by Shiraishi Calcium Co., Ltd.).
【0043】比較例2〜4 実施例1で使用したアストラプラス(成分;カオリン、
ヒューバー社製)100部を、カオグロス(成分;カオ
リン、ヒューバー社製)(比較例2)、アストラプレー
ト(成分;デラミカオリン、ヒューバー社製)(比較例
3)、ブリリアント(成分;軽質炭酸カルシウム、白石
カルシウム社製)(比較例4)に変更した以外は同様に
塗工紙を作成し、評価した。ここで比較例3,4につい
ては、キャレンダー処理条件を強化したが、光沢度は高
くならなかった。Comparative Examples 2 to 4 Astraplus used in Example 1 (components: kaolin,
100 parts of Huber), chao gloss (component; kaolin, manufactured by Huber) (Comparative Example 2), astraplate (component: Delamikaolin, manufactured by Huber) (Comparative Example 3), brilliant (component: light calcium carbonate, A coated paper was prepared and evaluated in the same manner except that the composition was changed to Shiraishi Calcium Co. (Comparative Example 4). Here, in Comparative Examples 3 and 4, the calendering conditions were enhanced, but the glossiness did not increase.
【0044】実施例3〜5 実施例1で使用したアストラプラス(成分;カオリン、
ヒューバー社製)100部を、アストラプラス(成分;
カオリン、ヒューバー社製)97.5部とHP91(成
分;中空有機顔料、ローム&ハース社製)2.5部(実
施例3)、アストラプラス(成分;カオリン、ヒューバ
ー社製)95部とHP91(成分;中空有機顔料、ロー
ム&ハース社製)5部(実施例4)、アストラプラス
(成分;カオリン、ヒューバー社製)90部とHP91
(成分;中空有機顔料、ローム&ハース社製)10部
(実施例5)、に変更した以外は同様に塗工紙を作成
し、評価した。Examples 3 to 5 Astraplus used in Example 1 (components: kaolin,
100 parts of Astra Plus (Huber).
97.5 parts of Kaolin, manufactured by Huber and HP91 (component: hollow organic pigment, manufactured by Rohm & Haas) 2.5 parts (Example 3), 95 parts of Astra Plus (component; kaolin, manufactured by Huber) and 95 parts of HP91 (Component: hollow organic pigment, manufactured by Rohm & Haas) 5 parts (Example 4), 90 parts of Astra Plus (component: kaolin, manufactured by Huber) and HP91
(Component: hollow organic pigment, manufactured by Rohm & Haas Co., Ltd.) A coated paper was prepared and evaluated in the same manner except that the amount was changed to 10 parts (Example 5).
【0045】比較例5 実施例1で使用したアストラプラス(成分;カオリン、
ヒューバー社製)100部を、アストラプラス(成分;
カオリン、ヒューバー社製)50部とカオグロス(成
分;カオリン、ヒューバー社製)50部に変更した以外
は同様に塗工紙を作成し、評価した。Comparative Example 5 Astraplus used in Example 1 (components: kaolin,
100 parts of Astra Plus (Huber).
Coated papers were prepared and evaluated in the same manner except that 50 parts of kaolin (manufactured by Huber) and 50 parts of chao gloss (component: kaolin, manufactured by Huber) were changed.
【0046】実施例6〜7 実施例4を、塗工量を8g/m2(絶乾固形量)(実施
例6)、18g/m2(実施例7)に変更した以外は同
様に塗工紙を作成し、評価した。Examples 6 to 7 The same procedures as in Example 4 were carried out except that the coating amount was changed to 8 g / m 2 (absolute dry solids) (Example 6) and 18 g / m 2 (Example 7). Paper was made and evaluated.
【0047】比較例6 実施例4を、塗工量を6g/m2(絶乾固形量)に変更
した以外は同様に塗工紙を作成し、評価した。Comparative Example 6 A coated paper was prepared and evaluated in the same manner as in Example 4, except that the coating amount was changed to 6 g / m 2 (absolute dry solid content).
【0048】実施例8〜9 実施例4を、平滑化処理後の光沢度を55%(実施例
8)、75%(実施例9)に変更した以外は同様に塗工
紙を作成し、評価した。Examples 8 to 9 Coated papers were prepared in the same manner as in Example 4 except that the glossiness after the smoothing treatment was changed to 55% (Example 8) and 75% (Example 9). evaluated.
【0049】実施例10 実施例4の紙基体の調成で、ポリアクリルアミド系樹脂
(商品名;PS117、荒川化学工業社製)の添加量を
0.4%と、ポリアクリルアミド系樹脂(商品名;PS
460、荒川化学工業社製)の添加量を0.6%に変更
(紙基体)した以外は同様に塗工紙を作成し、評価し
た。Example 10 In preparing the paper substrate of Example 4, the amount of polyacrylamide-based resin (trade name; PS117, manufactured by Arakawa Chemical Industry Co., Ltd.) was 0.4%, and the amount of polyacrylamide-based resin (trade name) was changed. ; PS
460, manufactured by Arakawa Chemical Industries Co., Ltd.), except that the amount of addition (paper base) was changed to 0.6%, and a coated paper was prepared and evaluated in the same manner.
【0050】比較例7 実施例4の紙基体の調成で、ポリアクリルアミド系樹脂
を添加せず、サイズプレスを水に変更(紙基体)した
以外は同様に塗工紙を作成し、評価した。Comparative Example 7 A coated paper was prepared and evaluated in the same manner as in Example 4, except that the polyacrylamide-based resin was not added, and the size press was changed to water (paper base). .
【0051】比較例8 実施例4の紙基体の調成で、ポリアクリルアミド系樹脂
(商品名;PS117荒川化学工業社製)の添加量を
0.7%と、ポリアクリルアミド系樹脂(商品名;PS
460 荒川化学工業社製)の添加量を0.8%に変更
(紙基体)した以外は同様に塗工紙を作成し、評価し
た。Comparative Example 8 In the preparation of the paper substrate of Example 4, the addition amount of polyacrylamide resin (trade name; PS117, manufactured by Arakawa Chemical Industry Co., Ltd.) was 0.7%, and polyacrylamide resin (trade name; PS
460 (Arakawa Chemical Industry Co., Ltd.), except that the amount of addition was changed to 0.8% (paper base).
【0052】評価方法 [顔料の平均粒子径と粒度分布の測定]測定器は、セデ
ィグラフ5100 V3.07を用いた。結果を表2に
示す。 Evaluation Method [Measurement of Average Particle Diameter and Particle Size Distribution of Pigment] A Sedigraph 5100 V3.07 was used as a measuring instrument. Table 2 shows the results.
【0053】[顔料のアスペクト比の測定と形状観察]
電子顕微鏡で15000倍に拡大して、アスペクト比の
測定と形状の観察を行った。結果を表2に示す。[Measurement of Aspect Ratio of Pigment and Observation of Shape]
The image was magnified 15,000 times with an electron microscope to measure the aspect ratio and observe the shape. Table 2 shows the results.
【0054】[紙基体および塗工紙の内部結合強さの測
定]測定方法は、J.TAPPI No.54−93に
準じて測定した。測定器はSCOTT社製インターナル
ボンドテスター MODEL−Bを用いた。[Measurement of Internal Bonding Strength of Paper Substrate and Coated Paper] TAPPI No. It measured according to 54-93. The measuring instrument used was an internal bond tester Model-B manufactured by SCOTT.
【0055】[紙基体と塗工紙の透気度の測定]王研式
透気度測定器によって測定した。[Measurement of Air Permeability of Paper Substrate and Coated Paper] The air permeability was measured by an Oken type air permeability meter.
【0056】[紙基体のベック平滑度の測定]ベック平
滑度測定器によって測定した[Measurement of Beck Smoothness of Paper Base] Measured by a Beck smoothness measuring device.
【0057】[塗工紙の光沢度の測定]光沢度を入射角
と受光角が75度の条件で測定した。測定器は、村上色
彩研究所社製GLOSS METER MODEL G
M−26Dを用いた。[Measurement of Glossiness of Coated Paper] The glossiness was measured under the conditions that the incident angle and the light receiving angle were 75 degrees. The measuring instrument is GLOSS METER MODEL G manufactured by Murakami Color Research Laboratory.
M-26D was used.
【0058】[塗工紙の印刷]印刷機は、小森コーポレ
ーション社製小森システムC−20を用い、下記条件で
印刷した 環境:20℃、65%RH 印刷速度:200〜250m/min 印刷長:6000m 乾燥条件:ガスヒーターを用い、紙面温度150℃に調
整[Printing of Coated Paper] A printing machine was used under the following conditions, using Komori System C-20 manufactured by Komori Corporation Environment: 20 ° C., 65% RH Printing speed: 200 to 250 m / min Printing length: 6000m Drying conditions: Adjust the paper surface temperature to 150 ° C using a gas heater
【0059】(塗工紙の印刷インキ受理性評価)下記の
評価基準で評価した。 ◎:網点の抜け、欠けが観られない。実用上問題なく、
品質も優れている。 ○:網点の抜け、欠けがやや観られる。実用上問題な
い。 △:網点の抜け、欠けが頻繁に観られる。実用上問題あ
る。 ×:網点の抜け、欠けが著しく観られる。実用上問題あ
り、品質も著しく劣っている。(Evaluation of Printing Ink Acceptability of Coated Paper) Evaluation was made according to the following evaluation criteria. :: No missing or missing dot. There is no problem in practical use,
The quality is also excellent. :: Missing or missing dots are slightly observed. No problem in practical use. Δ: Missing or missing dots are frequently observed. There is a practical problem. ×: Dropouts and chipping of dots are remarkably observed. There is a problem in practical use, and the quality is extremely poor.
【0060】(ブランケット汚れ評価)6000m印刷
後のブランケットの汚れを、下記の評価基準で評価し
た。 ◎:汚れが観られない。実用上問題なく、品質も優れて
いる。 ○:汚れがやや観られる。実用上問題ない。 △:汚れが頻繁に観られる。実用上問題ある。 ×:汚れが著しく観られた。実用上問題あり、品質も著
しく劣っている。(Evaluation of Stain on Blanket) Stain on the blanket after printing at 6000 m was evaluated according to the following evaluation criteria. A: No stain is observed. There is no practical problem and the quality is excellent. :: Dirt is slightly observed. No problem in practical use. Δ: Dirt is frequently observed. There is a practical problem. X: Stain was remarkably observed. There is a problem in practical use, and the quality is extremely poor.
【0061】(マクロブリスタ評価)マクロブリスタの
発生状態を拡大ルーペ(30倍)で確認し、下記の評価
基準で評価した。 ◎:マクロブリスタが観られない。実用上問題なく、品
質も優れている。 ○:マクロブリスタがやや観られる。実用上問題ない。 △:マクロブリスタが頻繁に観られる。実用上問題あ
る。 ×:マクロブリスタが著しく観られた。実用上問題あ
り、品質も著しく劣っている。(Evaluation of Macro Blister) The state of occurrence of macro blisters was confirmed with a magnifying loupe (30 times) and evaluated according to the following evaluation criteria. :: Macro blister was not observed. There is no practical problem and the quality is excellent. :: Macro blister is slightly observed. No problem in practical use. Δ: Macro blisters are frequently observed. There is a practical problem. X: Macro blister was remarkably observed. There is a problem in practical use, and the quality is extremely poor.
【0062】(ミクロブリスタ評価)ミクロブリスタの
発生状態を拡大ルーペ(30倍)で確認し、下記の評価
基準で評価した。 ◎:ミクロブリスタが観られない。実用上問題なく、品
質も優れている。 ○:ミクロブリスタがやや観られる。実用上問題ない。 △:ミクロブリスタが頻繁に観られる。実用上問題あ
る。 ×:ミクロブリスタが著しく観られた。実用上問題あ
り、品質も著しく劣っている。(Evaluation of Micro Blister) The state of occurrence of micro blisters was confirmed with a magnifying loupe (30 times) and evaluated according to the following evaluation criteria. :: Micro blister was not observed. There is no practical problem and the quality is excellent. :: Micro blisters are slightly observed. No problem in practical use. Δ: Micro blisters are frequently observed. There is a practical problem. X: Micro blisters were remarkably observed. There is a problem in practical use, and the quality is extremely poor.
【0063】〔紙基体および塗工紙の評価〕以上より、
紙基体、および得られた塗工紙の透気度、光沢度および
内部結合強さの結果を表1および表3に示す。また得ら
れた塗工紙の印刷インキの受理性、ブランケットの汚れ
並びにブリスタの評価を行った。結果は表4に示す。[Evaluation of Paper Substrate and Coated Paper]
Tables 1 and 3 show the results of the air permeability, glossiness and internal bond strength of the paper substrate and the obtained coated paper. The printing paper was evaluated for acceptability of printing ink, contamination of blanket and blister. The results are shown in Table 4.
【0064】[0064]
【表1】 [Table 1]
【0065】[0065]
【表2】 [Table 2]
【0066】[0066]
【表3】 [Table 3]
【0067】[0067]
【表4】 [Table 4]
【0068】[0068]
【発明の効果】 本発明に係る塗工紙は、白紙の光沢度
が高く、かつオフセット印刷におけるインクの受理性に
優れ、ブリスタの発生がなく、高品位な画像が得られる
塗工紙であり、実用上極めて有用である。EFFECT OF THE INVENTION The coated paper according to the present invention is a coated paper that has high glossiness of white paper, is excellent in ink receptivity in offset printing, has no blistering, and can obtain high-quality images. It is extremely useful in practice.
Claims (3)
主成分とする塗被層とを設けてなる塗工紙において、前
記塗被層中の顔料100重量部中に、アスペクト比5〜
15、平均粒子径0.3〜1.0μmのカオリンを60
重量部以上含み、かつ前記塗工紙の、塗被層表面の白紙
光沢度が50〜80%、透気度が7000秒以下および
J.TAPPI No.54−93に準じる内部結合強
さが0.27〜0.85KJ/m2であることを特徴と
する塗工紙。1. A coated paper comprising a paper base material and a coating layer mainly composed of a pigment and an adhesive provided on both surfaces thereof, wherein 100 parts by weight of the pigment in the coating layer have an aspect ratio of Ratio 5
15, kaolin having an average particle size of 0.3 to 1.0 μm is mixed with 60
The coated paper has a white paper glossiness of 50 to 80%, an air permeability of 7000 seconds or less, and J.I. TAPPI No. Coated paper, wherein the internal bond strength is 0.27~0.85KJ / m 2 analogous to 54-93.
0.5〜1.5μmの中空有機顔料を1〜10重量部含
む請求項1記載の塗工紙。2. The coated paper according to claim 1, wherein 100 parts by weight of the pigment contains 1 to 10 parts by weight of a hollow organic pigment having an average particle size of 0.5 to 1.5 μm.
下、かつ透気度が40秒以下である請求項1記載の塗工
紙。3. The coated paper according to claim 1, wherein the paper base material has a Beck smoothness of 50 seconds or less and an air permeability of 40 seconds or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11024171A JP2000226791A (en) | 1999-02-01 | 1999-02-01 | Coated paper |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11024171A JP2000226791A (en) | 1999-02-01 | 1999-02-01 | Coated paper |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007281646A Division JP2008088625A (en) | 2007-10-30 | 2007-10-30 | Coated paper |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000226791A true JP2000226791A (en) | 2000-08-15 |
Family
ID=12130911
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11024171A Pending JP2000226791A (en) | 1999-02-01 | 1999-02-01 | Coated paper |
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JP (1) | JP2000226791A (en) |
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---|---|---|---|---|
JP2000282397A (en) * | 1999-03-31 | 2000-10-10 | Nippon Paper Industries Co Ltd | Base paper for release paper |
JP2002317397A (en) * | 2001-04-23 | 2002-10-31 | Mitsubishi Paper Mills Ltd | Coated paper for offset printing for environmentally friendly inks and easily deinkable printed matter |
US6942919B2 (en) | 2001-03-28 | 2005-09-13 | Oji Paper Co., Ltd. | Coated paper sheet |
JP2006052518A (en) * | 2004-07-16 | 2006-02-23 | Nippon Paper Industries Co Ltd | Coated paper for gravure printing |
JP2006057229A (en) * | 2004-07-09 | 2006-03-02 | Nippon Paper Industries Co Ltd | Coated paper for offset printing |
JP2006057230A (en) * | 2004-07-21 | 2006-03-02 | Nippon Paper Industries Co Ltd | Coated paper for offset printing |
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JP2006193721A (en) * | 2004-12-15 | 2006-07-27 | Oji Paper Co Ltd | Pressure sensitive adhesive sheet |
JP2006225815A (en) * | 2005-02-21 | 2006-08-31 | Daio Paper Corp | Coated paper for printing |
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WO2007016002A1 (en) * | 2005-08-01 | 2007-02-08 | Hewlett-Packard Development Company, L.P. | Porous pigment coating |
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JP2009133028A (en) * | 2007-11-30 | 2009-06-18 | Nisshinbo Holdings Inc | Coated paper |
JP2009155788A (en) * | 2007-12-26 | 2009-07-16 | Marusumi Paper Co Ltd | Coated newsprint for offset printing |
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JP2000282397A (en) * | 1999-03-31 | 2000-10-10 | Nippon Paper Industries Co Ltd | Base paper for release paper |
US6942919B2 (en) | 2001-03-28 | 2005-09-13 | Oji Paper Co., Ltd. | Coated paper sheet |
JP2002317397A (en) * | 2001-04-23 | 2002-10-31 | Mitsubishi Paper Mills Ltd | Coated paper for offset printing for environmentally friendly inks and easily deinkable printed matter |
JP2009174113A (en) * | 2003-06-30 | 2009-08-06 | Oji Paper Co Ltd | Coated paper |
US7160608B2 (en) | 2003-06-30 | 2007-01-09 | Oji Paper Co., Ltd. | Coated paper |
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JP2006193721A (en) * | 2004-12-15 | 2006-07-27 | Oji Paper Co Ltd | Pressure sensitive adhesive sheet |
JP2006188800A (en) * | 2005-01-07 | 2006-07-20 | Oji Paper Co Ltd | Coated paper |
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WO2007016002A1 (en) * | 2005-08-01 | 2007-02-08 | Hewlett-Packard Development Company, L.P. | Porous pigment coating |
US7618701B2 (en) | 2005-08-01 | 2009-11-17 | Hewlett-Packard Development Company, L.P. | Porous pigment coating |
KR101254836B1 (en) * | 2005-08-01 | 2013-04-15 | 휴렛-팩커드 디벨롭먼트 컴퍼니, 엘.피. | Porous pigment coating |
JP4494351B2 (en) * | 2006-02-28 | 2010-06-30 | 富士フイルム株式会社 | Thermal transfer image-receiving sheet and method for producing the same |
JP2007230048A (en) * | 2006-02-28 | 2007-09-13 | Fujifilm Corp | Thermal transfer image-receiving sheet and method for producing the same |
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