JP4436418B2 - Process paper - Google Patents
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- JP4436418B2 JP4436418B2 JP2008052376A JP2008052376A JP4436418B2 JP 4436418 B2 JP4436418 B2 JP 4436418B2 JP 2008052376 A JP2008052376 A JP 2008052376A JP 2008052376 A JP2008052376 A JP 2008052376A JP 4436418 B2 JP4436418 B2 JP 4436418B2
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- 238000000034 method Methods 0.000 title claims description 53
- 238000000576 coating method Methods 0.000 claims description 47
- 239000011248 coating agent Substances 0.000 claims description 45
- 239000011247 coating layer Substances 0.000 claims description 41
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 36
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 36
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 36
- 239000000853 adhesive Substances 0.000 claims description 32
- 239000000049 pigment Substances 0.000 claims description 31
- 230000001070 adhesive effect Effects 0.000 claims description 30
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 27
- 229920002125 Sokalan® Polymers 0.000 claims description 24
- 239000004584 polyacrylic acid Substances 0.000 claims description 22
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 16
- 229920000126 latex Polymers 0.000 claims description 15
- 239000004816 latex Substances 0.000 claims description 15
- 239000010410 layer Substances 0.000 claims description 15
- 239000002344 surface layer Substances 0.000 claims description 13
- 238000002156 mixing Methods 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 230000035699 permeability Effects 0.000 claims description 10
- 230000007423 decrease Effects 0.000 claims description 9
- 238000012545 processing Methods 0.000 claims description 9
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 8
- 239000004927 clay Substances 0.000 claims description 8
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 8
- 239000005018 casein Substances 0.000 claims description 7
- 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 claims description 7
- 235000021240 caseins Nutrition 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 7
- 239000002174 Styrene-butadiene Substances 0.000 claims description 6
- 239000000178 monomer Substances 0.000 claims description 6
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 5
- 239000011115 styrene butadiene Substances 0.000 claims description 5
- 239000000123 paper Substances 0.000 description 89
- 239000002904 solvent Substances 0.000 description 29
- 239000002585 base Substances 0.000 description 17
- 239000010893 paper waste Substances 0.000 description 15
- 239000002649 leather substitute Substances 0.000 description 12
- 239000002798 polar solvent Substances 0.000 description 12
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 229920001131 Pulp (paper) Polymers 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- 229920000915 polyvinyl chloride Polymers 0.000 description 7
- 239000004800 polyvinyl chloride Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 102000011632 Caseins Human genes 0.000 description 6
- 108010076119 Caseins Proteins 0.000 description 6
- 239000012454 non-polar solvent Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 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 5
- 239000000047 product Substances 0.000 description 5
- 239000005995 Aluminium silicate Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- 235000012211 aluminium silicate Nutrition 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 239000010419 fine particle Substances 0.000 description 3
- 239000011121 hardwood Substances 0.000 description 3
- -1 satin white Chemical compound 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 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
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000006081 fluorescent whitening agent Substances 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920000306 polymethylpentene Polymers 0.000 description 2
- 239000011116 polymethylpentene Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 239000011122 softwood Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000007754 air knife coating Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 description 1
- 235000010261 calcium sulphite Nutrition 0.000 description 1
- 239000004202 carbamide 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
- 230000015556 catabolic process Effects 0.000 description 1
- 229920006319 cationized starch Polymers 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000002655 kraft paper Substances 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
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000013054 paper strength agent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Paper (AREA)
Description
本発明は、有機溶剤に対する耐性に優れた工程紙に関するものである。より詳しくは、有機溶剤を用いて製造する合成皮革の工程紙などとして利用するに好適な工程紙に関するものである。 The present invention relates to a process paper excellent in resistance to an organic solvent. More specifically, the present invention relates to a process paper suitable for use as a process paper for synthetic leather produced using an organic solvent.
塗工紙、特に塗工層がキャストコート法により設けられたキャスト塗工紙は、産業用基材(例えば、マーキングシート、金属箔等の剥離紙など。)、包装用紙(例えば、紙袋、ブックカバーなど。)、工程原紙(例えば、合成皮革やプラスチックフィルム等の工程原紙。)などとして多用されている。なかでも工程紙は、例えば、キャスト塗工紙上に溶剤と混合したモノマーを展開し、熱や電子線でモノマー同士を反応させ、もってプラスチックフィルムなどを得る。 The coated paper, especially the cast coated paper in which the coating layer is provided by the cast coating method, is an industrial substrate (for example, a marking sheet, a release sheet such as a metal foil), packaging paper (for example, a paper bag, a book). Cover, etc.), process base paper (for example, process base paper such as synthetic leather and plastic film), etc. In particular, for the process paper , for example, a monomer mixed with a solvent is developed on cast coated paper, and the monomers are reacted with each other by heat or electron beam, thereby obtaining a plastic film.
そこで、この種の工程紙は、耐溶剤性に優れることが望まれ、例えば、接着剤としてゲル含量が85%以上であるスチレン・ブタジエン系共重合体ラテックスを使用するキャスト塗工紙が提案されている(例えば、特許文献1参照。)。 Therefore, this type of process paper is desired to have excellent solvent resistance. For example, cast coated paper using a styrene / butadiene copolymer latex having a gel content of 85% or more as an adhesive has been proposed. (For example, refer to Patent Document 1).
一方、近年、環境負荷低減の目的で、使用される有機溶剤が、非極性溶剤から極性溶剤に移行しつつあり、工程原紙などには極性溶剤及び非極性溶剤の両方に対する耐溶剤性が求められている。しかも、耐溶剤性に関する要求も厳しくなっており、単に繰り返し使用しても塗工層が剥離し難いなどというものではなく、写像性や光沢度なども低下し難いといった高度の品質が求められるようになっている。 On the other hand, in recent years, the organic solvent used has been shifting from a nonpolar solvent to a polar solvent for the purpose of reducing the environmental load, and process base paper and the like are required to have solvent resistance against both the polar solvent and the nonpolar solvent. ing. In addition, the requirements regarding solvent resistance are becoming stricter, and it is not said that the coating layer is difficult to peel off even if it is repeatedly used, and high quality such that image clarity and glossiness are not easily lowered is required. It has become.
しかしながら、従来の工程紙は、これらの要求を満足するには至っていない。また、キャスト塗工紙は、キャストドラム表面温度が高温であると、塗工層がキャストドラムに圧接された際に、塗工層中の水分が急激に沸騰して塗工層が破壊され、無数の微細なピンホール(いわゆるマイクロピット)が発生してしまう。したがって、キャストドラム表面温度を高温にすることができず、乾燥速度の低下、生産速度の低下を招く。
本発明が解決しようとする主たる課題は、極性溶剤及び非極性溶剤の両方に対して、優れた耐溶剤性を発揮する塗工紙を提供することにある。更には、光沢度が高く、写像性の低下が少ないため製造する合成皮革の鏡面性の低下が少なく、マイクロピットの発生が少ないため見栄えの良い合成皮革を製造できる、合成皮革工程紙として利用可能な工程紙を提供することにある。 The main problem to be solved by the present invention is to provide a coated paper exhibiting excellent solvent resistance against both polar and nonpolar solvents. Furthermore, it can be used as a synthetic leather process paper that has a high glossiness and is less likely to cause poor visual clarity due to less degradation of the mirror surface of the synthetic leather produced and less micropits. Is to provide a simple process paper .
この課題を解決した本発明は、次のとおりである。
〔請求項1記載の発明〕
原紙と、この原紙の少なくとも一方の面に設けられた顔料及び接着剤を主成分とする1層以上の塗工層とを有する工程紙であって、
前記接着剤が、ポリアクリル酸及びポリビニルアルコールの両方を合計配合量が前記顔料100質量部に対して1〜20質量部となるように含み、
前記顔料が、クレーを当該顔料100質量部に対して20〜80質量部含み、
前記塗工層の表面層が、塗工量20〜40g/m2とされ、かつキャストコート法で鏡面処理されている、
ことを特徴とする工程紙。
The present invention that has solved this problem is as follows.
[Invention of Claim 1]
And base paper, a process paper having a least one layer of the coating layer composed mainly pigment and an adhesive provided on at least one surface of the base paper,
The adhesive contains both polyacrylic acid and polyvinyl alcohol so that the total blending amount is 1 to 20 parts by mass with respect to 100 parts by mass of the pigment ,
The pigment contains 20 to 80 parts by mass of clay with respect to 100 parts by mass of the pigment;
The surface layer of the coating layer has a coating amount of 20 to 40 g / m 2 and is mirror-finished by a cast coating method.
Process paper characterized by that .
〔請求項2記載の発明〕
前記顔料が、重質炭酸カルシウムを当該顔料100質量部に対して20〜80質量部含む、
請求項1記載の工程紙。
〔請求項3記載の発明〕
前記接着剤が、カゼインを前記顔料100質量部に対して1〜15質量部含み、スチレン−ブタジエンラテックスを前記顔料100質量部に対して3〜30質量部含む、
請求項1又は請求項2記載の工程紙。
〔請求項4記載の発明〕
前記ポリアクリル酸及び前記ポリビニルアルコールが共重合している、
請求項1〜3のいずれか1項に記載の工程紙。
[Invention of Claim 2]
The pigment contains 20 to 80 parts by mass of heavy calcium carbonate with respect to 100 parts by mass of the pigment.
The process paper according to claim 1.
[Invention of Claim 3]
The adhesive contains 1 to 15 parts by mass of casein with respect to 100 parts by mass of the pigment, and 3 to 30 parts by mass of styrene-butadiene latex with respect to 100 parts by mass of the pigment.
The process paper according to claim 1 or 2.
[Invention of Claim 4]
The polyacrylic acid and the polyvinyl alcohol are copolymerized,
The process paper of any one of Claims 1-3.
〔請求項5記載の発明〕
前記接着剤に含まれる、ポリアクリル酸と、ポリビニルアルコールとが、10:90〜90:10のモル比(単量体として含まれるものも共重合体として含まれるものも含む合計モル量のモル比)とされている、
請求項1〜4のいずれか1項に記載の工程紙。
[Invention of Claim 5 ]
The polyacrylic acid and polyvinyl alcohol contained in the adhesive have a molar ratio of 10:90 to 90:10 (a total molar amount including both a monomer and a copolymer). Ratio) ,
The process paper of any one of Claims 1-4 .
〔請求項6記載の発明〕
前記塗工層の表面層が、塗工量25〜35g/m2とされ、
JIS P 8119に基づいて測定したベック平滑度が500〜3000秒、Tappi T536cm−02に基づいて測定した透気度が1000〜3000秒とされている、
請求項1〜5のいずれか1項に記載の工程紙。
[Invention of Claim 6 ]
The surface layer of the coating layer has a coating amount of 25 to 35 g / m 2 ,
The Beck smoothness measured based on JIS P 8119 is 500 to 3000 seconds, and the air permeability measured based on Tappi T536cm-02 is 1000 to 3000 seconds.
The process paper of any one of Claims 1-5 .
〔請求項7記載の発明〕
次記処理を行ったときのJIS H 8686−2に基づいて測定した写像性の低下率が20%以下とされている、
請求項1〜6のいずれか1項に記載の工程紙。
(処理)
前記塗工層表面にメチルエチルケトン(MEK)又はトルエンを1g/m2の塗工量となるようにNo.2のワイヤーバーで塗工し、30秒経過してから90秒間130℃に加熱する。
[Invention of Claim 7 ]
The rate of decrease in image clarity measured based on JIS H 8686-2 when the following processing is performed is 20% or less.
The process paper of any one of Claims 1-6 .
(processing)
The coating layer surface was coated with methyl ethyl ketone (MEK) or toluene so that the coating amount was 1 g / m 2 . 2. Coat with 2 wire bars and heat to 130 ° C. for 90 seconds after 30 seconds.
〔請求項8記載の発明〕
前記塗工層上に剥離剤を塗布して剥離層を設けた、
請求項1〜7のいずれか1項に記載の工程紙。
[Invention of Claim 8 ]
A release layer was provided by applying a release agent on the coating layer,
Step paper according to any one of claims 1-7.
本発明によると、極性溶剤及び非極性溶剤の両方に対して、優れた耐溶剤性を発揮し、マイクロピットの発生が少ない工程紙となる。 According to the present invention, the process paper exhibits excellent solvent resistance with respect to both a polar solvent and a nonpolar solvent, and generates less micropits .
次に、本発明の実施の形態を説明する。
まず、本発明者らは、工程紙における極性溶剤への耐性を向上させる目的で鋭意研究を重ねた結果、塗工層の接着剤の種類と配合量とを規定することが有効であることを知見した。
すなわち、本発明者らは、原紙と、この原紙の少なくとも一方の面に設けられた顔料及び接着剤を主成分とする塗工層と有する塗工紙について、接着剤が、ポリアクリル酸及びポリビニルアルコールの両方、ポリアクリル酸−ポリビニルアルコール共重合体、又は、ポリアクリル酸とポリビニルアルコールとポリアクリル酸−ポリビニルアルコール共重合体とを含むことで、優れた耐溶剤性が発揮されることを知見し、本発明を完成するに至った。
Next, an embodiment of the present invention will be described.
First, the present inventors have conducted extensive research for the purpose of improving resistance to polar solvents in process paper , and as a result, it is effective to specify the type and amount of adhesive in the coating layer. I found out.
That is, the present inventors have made a coating paper having a base paper and a coating layer mainly composed of a pigment and an adhesive provided on at least one surface of the base paper. It is found that excellent solvent resistance is exhibited by including both alcohol, polyacrylic acid-polyvinyl alcohol copolymer, or polyacrylic acid, polyvinyl alcohol, and polyacrylic acid-polyvinyl alcohol copolymer. Thus, the present invention has been completed.
接着剤としては、少なくとも、ポリアクリル酸(PAA)及びポリビニルアルコール(PVA)の両方、又は、ポリアクリル酸−ポリビニルアルコール共重合体を配合することが必須である。ポリアクリル酸又はポリビニルアルコールのみを配合した場合は、極性溶剤又は非極性溶剤に対する耐性が低く、塗工面が極性溶剤に侵食され易くなる。特に合成皮革工程紙とする場合は、繰り返し使用に耐えないものとなる。 As an adhesive, it is essential to blend at least both polyacrylic acid (PAA) and polyvinyl alcohol (PVA) or a polyacrylic acid-polyvinyl alcohol copolymer. When only polyacrylic acid or polyvinyl alcohol is blended, resistance to a polar solvent or nonpolar solvent is low, and the coated surface is easily eroded by the polar solvent. In particular, when a synthetic leather process paper is used, it cannot withstand repeated use.
ポリアクリル酸とポリビニルアルコールとの割合は、単に混合した場合(単量体の場合)と、共重合体の場合の合計を、モル比で規定することができ、好ましくはPAA:PVA=10:90〜90:10であり、より好ましくはPAA:PVA=15:85〜85:15である。PAAが10モル%未満では、PAAそのものの性質(硬質樹脂であり、室温で剛性を有する、耐水性と接着強度に優れる性質)が発現されにくく、また、90モル%を超過すると、PVA成分が少なくなり、PVAの性質(軟質樹脂であり、室温で柔軟性を有する、耐水性と接着強度に優れる性質)が発現され難くなる。PAAとPVAとを共重合すると、耐溶剤性が向上する理由は不明だか、いずれも耐水性を有する硬質樹脂と軟質樹脂とを組み合わせて、室温において、塗工紙表面に柔軟性と剛性の双方を付与することで、メチルエチルケトン(MEK)を始めとする極性溶剤及びトルエンを始めとする非極性溶剤に対する耐性が向上すると考えられる。また、ポリアクリル酸及びポリビニルアルコールの両方を含ませるよりも、ポリアクリル酸−ポリビニルアルコール共重合体を含ませる方が好ましい。これは、ポリアクリル酸とポリビニルアルコールとの混合物に比べて、共重合体の方がより均一に、より分子レベルでの混合が可能となるためである。分子レベルで混合することにより、溶剤接触によるミクロレベルでの変化が発生しても、変化を柔軟に緩和しながら、塗工面としての剛性を失わないため、写像性の低下が防止できる。 The ratio of polyacrylic acid and polyvinyl alcohol can be defined by the molar ratio of the case of simply mixing (in the case of monomer) and the case of copolymer, preferably PAA: PVA = 10: It is 90-90: 10, More preferably, it is PAA: PVA = 15: 85-85: 15. If the PAA is less than 10 mol%, the properties of the PAA itself (hard resin, rigid at room temperature, and excellent water resistance and adhesive strength) are difficult to be expressed. As a result, the properties of PVA (a soft resin that has flexibility at room temperature and has excellent water resistance and adhesive strength) are hardly exhibited. Copolymerization of PAA and PVA is unclear why the solvent resistance is improved, or both are combined with a hard resin and a soft resin that have water resistance, and both flexibility and rigidity are applied to the coated paper surface at room temperature. It is considered that the resistance to polar solvents such as methyl ethyl ketone (MEK) and nonpolar solvents such as toluene is improved. Moreover, it is more preferable to include a polyacrylic acid-polyvinyl alcohol copolymer than to include both polyacrylic acid and polyvinyl alcohol. This is because the copolymer can be more uniformly mixed at a molecular level than the mixture of polyacrylic acid and polyvinyl alcohol. By mixing at the molecular level, even if a change at the micro level due to solvent contact occurs, the change as a coating surface is not lost while the change is flexibly relaxed.
以上の本形態に必須の接着剤、すなわち、ポリアクリル酸、ポリビニルアルコール及びポリアクリル酸−ポリビニルアルコール共重合体の合計配合量は、顔料100質量部に対して、好ましくは1〜20質量部、より好ましくは2〜15質量部である。1質量部未満では、耐溶剤性の効果が十分に発現せず耐溶剤性に劣り、20質量部を超過すると、顔料由来の平滑性や光沢性が低下し、見栄えが悪化するだけでなく、平滑性の低い部分に極性溶剤が溜まりやすく、局所的に侵食が進みやすくなる。 Adhesives essential for the present embodiment, that is, the total blending amount of polyacrylic acid, polyvinyl alcohol and polyacrylic acid-polyvinyl alcohol copolymer is preferably 1 to 20 parts by mass with respect to 100 parts by mass of the pigment, More preferably, it is 2-15 mass parts. When the amount is less than 1 part by mass, the solvent resistance effect is not sufficiently exhibited and the solvent resistance is inferior. When the amount exceeds 20 parts by mass, not only the pigment-derived smoothness and gloss are deteriorated, but the appearance is deteriorated. Polar solvent tends to accumulate in a portion with low smoothness, and erosion tends to proceed locally.
本形態においては、接着剤以外にも、耐溶剤性を阻害しない範囲で、塗工紙製造で一般的に用いられる接着剤を併用することができる。具体的には、例えば、カゼイン、大豆蛋白等の蛋白質類;スチレン−ブタジエン共重合体ラテックス、メチルメタクリレート−ブタジエン共重合体ラテックス、スチレン−メチルメタクリレート−ブタジエン共重合体ラテックス等の共役ジエン系ラテックス;アクリル酸エステル及び/又はメタクリル酸エステルの重合体ラテックス若しくは共重合体ラテックス等のアクリル系ラテックス;エチレン−酢酸ビニル重合体ラテックス等のビニル系ラテックス;これらの各種共重合体ラテックスをカルボキシル基等の官能基含有単量体で変性したアルカリ部分溶解性又は非溶解性のラテックス等のラテックス類;オレフィン−無水マレイン酸樹脂、メラミン樹脂、尿素樹脂、ウレタン樹脂等の合成樹脂系接着剤;酸化澱粉、陽性化澱粉、エステル化澱粉、デキストリン等の澱粉類;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等を挙げることができ、これらの中から1種又は2種以上を適宜選択して使用することができる。 In this embodiment, in addition to the adhesive, an adhesive generally used in coated paper production can be used in combination as long as the solvent resistance is not impaired. Specifically, for example, proteins such as casein and soybean protein; conjugated diene latexes such as styrene-butadiene copolymer latex, methyl methacrylate-butadiene copolymer latex, styrene-methyl methacrylate-butadiene copolymer latex; Acrylic latex such as acrylic acid ester and / or methacrylic acid ester polymer latex or copolymer latex; vinyl latex such as ethylene-vinyl acetate polymer latex; Latexes such as alkali partially soluble or insoluble latex modified with group-containing monomers; synthetic resin adhesives such as olefin-maleic anhydride resin, melamine resin, urea resin, urethane resin; oxidized starch, positive Starch, ester Starches, starches such as dextrin; carboxymethyl cellulose, may be mentioned cellulose derivatives such as hydroxyethyl cellulose, it can be used by selecting one or more from among these as appropriate.
これらの一般的に用いられる接着剤成分の種類と配合量は、使用用途によって異なる。具体的には、例えば、合成皮革工程紙の場合は、高光沢塗工層を設けるため、キャスト塗工を行うのが一般的であり、カゼインやスチレン−ブタジエンラテックスが好適に用いられる。カゼインはキャストドラムからの剥離性を向上させるために配合し、好ましくは1〜15質量部である。1質量部未満では、剥離性が低下し、塗工面の一部がキャストドラムに付着するトラブルが発生しやすくなる。他方、15質量部を超過すると剥離性能が頭打ちとなり、高価なカゼインを大量使用する意味がなく経済性に劣る。スチレン−ブタジエンラテックスは、顔料由来の光沢性を塗工紙に発現させる働きをし、好ましくは3質量部〜30質量部である。3質量部未満では十分な光沢と接着力とが発現せず、逆に、30質量部を超えてもフィルム状の表面が形成され、顔料由来の光沢性が低下する。また、本件発明に必須の接着剤と、これら一般的に用いられる接着剤の配合量合計は、顔料100質量部に対して、好ましくは5〜60質量部である。5質量部未満では、耐溶剤性や剥離性、光沢性に劣り、他方、60質量部を超えても光沢性が低下するうえに、経済性に劣る。 The types and amounts of these commonly used adhesive components vary depending on the intended use. Specifically, for example, in the case of synthetic leather process paper, in order to provide a high gloss coating layer, cast coating is generally performed, and casein or styrene-butadiene latex is preferably used. Casein is blended in order to improve the peelability from the cast drum, and preferably 1 to 15 parts by mass. If it is less than 1 part by mass, the releasability is lowered, and a trouble that a part of the coated surface adheres to the cast drum tends to occur. On the other hand, if it exceeds 15 parts by mass, the peeling performance reaches its peak, and there is no point in using a large amount of expensive casein, resulting in poor economic efficiency. The styrene-butadiene latex has a function of developing the gloss derived from the pigment in the coated paper, and is preferably 3 parts by mass to 30 parts by mass. If the amount is less than 3 parts by mass, sufficient gloss and adhesive strength are not exhibited. Conversely, if the amount exceeds 30 parts by mass, a film-like surface is formed and the gloss derived from the pigment decreases. The total amount of the adhesive essential to the present invention and these commonly used adhesives is preferably 5 to 60 parts by mass with respect to 100 parts by mass of the pigment. If the amount is less than 5 parts by mass, the solvent resistance, peelability, and gloss are inferior. On the other hand, if the amount exceeds 60 parts by mass, the gloss is lowered and the economy is inferior.
塗工層に使用する顔料は特に限定されないが、例えば、カオリン、デラミネーテッドカオリン、タルク、クレー、軽質炭酸カルシウム、重質炭酸カルシウム、サチンホワイト、亜硫酸カルシウム、石膏、硫酸バリウム、ホワイトカーボン、焼成カオリン、構造化カオリン、珪藻土、炭酸マグネシウム、二酸化チタン、水酸化アルミニウム、水酸化カルシウム、シリカ、水酸化マグネシウム、水酸化亜鉛、酸化亜鉛、酸化マグネシウム、ベントナイト、セリサイト等の無機顔料やポリスチレン樹脂微粒子、尿素ホルマリン樹脂微粒子、微小中空粒子、多孔質微粒子等の有機顔料等の中から、1種又は2種以上を適宜選択して使用することができる。 The pigment used in the coating layer is not particularly limited. For example, kaolin, delaminated kaolin, talc, clay, light calcium carbonate, heavy calcium carbonate, satin white, calcium sulfite, gypsum, barium sulfate, white carbon, baking Inorganic pigments such as kaolin, structured kaolin, diatomaceous earth, magnesium carbonate, titanium dioxide, aluminum hydroxide, calcium hydroxide, silica, magnesium hydroxide, zinc hydroxide, zinc oxide, magnesium oxide, bentonite, sericite, and polystyrene resin fine particles One or more kinds of organic pigments such as urea formalin resin fine particles, fine hollow particles, and porous fine particles can be appropriately selected and used.
以上の顔料の中でもクレーは、光沢性及び平滑性に優れることから、顔料100質量部に対して、20質量部〜80質量部配合させるのが好ましい。配合量が20質量部未満では光沢性及び平滑性が劣るため耐溶剤性が低下しやすく、他方、80質量部を超過すると、塗工液の流動性が悪化して塗工時のプロファイルが悪化し、光沢や平滑のムラが発生し易くなるため、耐溶剤性が低下する。 Among the above pigments, clay is excellent in gloss and smoothness, and therefore it is preferable to blend 20 parts by mass to 80 parts by mass with respect to 100 parts by mass of the pigment. If the blending amount is less than 20 parts by mass, the glossiness and smoothness are inferior, so that the solvent resistance tends to be lowered. On the other hand, if it exceeds 80 parts by mass, the fluidity of the coating liquid is deteriorated and the profile at the time of coating is deteriorated. However, since gloss and smooth unevenness are likely to occur, the solvent resistance decreases.
クレーと併用する顔料としては、白色度を向上させ見栄えを良くし、かつ、経済性が良好な重質炭酸カルシウムが好ましい。この配合量は、クレーの配合量を補完するよう、20〜80質量部が好ましい。 As the pigment to be used in combination with clay, heavy calcium carbonate is preferred, which improves whiteness, improves appearance, and is economical. The blending amount is preferably 20 to 80 parts by mass so as to complement the blending amount of clay.
本形態の塗工剤には、顔料、接着剤の他にも、例えば、蛍光増白剤、蛍光増白剤の被染着物質、消泡剤、離型剤、着色剤、保水剤等の通常使用される各種助剤を適宜配合することもできる。 In addition to pigments and adhesives, the coating agent of the present embodiment includes, for example, fluorescent whitening agents, fluorescent whitening agent dyed substances, antifoaming agents, mold release agents, coloring agents, water retention agents, etc. Various auxiliary agents that are usually used can be appropriately blended.
原紙の表面への塗工剤の塗工は、塗工層を1層とする場合は、当該塗工層が表面層になるため、キャストコート法による。また、塗工層を2層以上とする場合は、表面層(最も外側にある層)をキャストコート法による。キャストコート法は、一般に、(1)塗工層が湿潤状態にある間に、鏡面仕上げした加熱ドラム(キャストドラム)に圧着(圧接)して乾燥するウェットキャスト法(直接法)、(2)湿潤状態の塗工層を一旦(半)乾燥した後に再湿潤液により膨潤可塑化(湿潤)させて、鏡面仕上げした加熱ドラムに圧着し乾燥するリウェットキャスト法(再湿潤法)、(3)湿潤状態の塗工層を凝固液等の凝固処理によりゲル状態にして、鏡面仕上げした加熱ドラムに圧着し乾燥するゲル化キャスト法(凝固法)の3種類に分けることができ、いずれの方法でも耐溶剤性を得られる。 The coating of the coating agent on the surface of the base paper is performed by a cast coating method when the coating layer is a single layer because the coating layer becomes a surface layer. In addition, when the number of coating layers is two or more, the surface layer (the outermost layer) is formed by a cast coating method. In general, the cast coating method includes (1) a wet cast method (direct method) in which a coated layer is in a wet state and is pressed (pressed) on a mirror-finished heating drum (cast drum) and dried (2) Rewetting cast method (rewetting method) in which the coating layer in a wet state is once (semi-) dried and then swollen and plasticized (wet) with a rewetting liquid, and then pressed onto a mirror-finished heating drum and dried (3) Wetting The coating layer in a state can be divided into three types: gelation cast method (coagulation method) in which the coating layer is made into a gel state by coagulation treatment with a coagulating liquid and then pressed onto a mirror-finished heating drum and dried. Solvent property can be obtained.
原紙の表面への塗工剤の塗工は、一般の塗工紙用途設備で行えば足り、例えば、ブレードコーター、エアーナイフコーター、トランスファーロールコーター、ロッドメタリングサイズプレスコーター、カーテンコーター等の塗工装置を設けたオンマシンコーター又はオフマシンコーターによって、原紙上に一層又は多層に分けて塗工剤を塗工できる。中でも、塗工層表面の高い平坦性が確保されるという点から、ブレードコーターを用いることが好ましい。また、ドライヤーパートでの乾燥方法としては、例えば、熱風加熱、ガスヒーター加熱、赤外線ヒーター加熱等の各種加熱乾燥方式を適宜採用することができる。 The coating of the coating agent on the surface of the base paper is sufficient if it is performed using general coating paper equipment, for example, blade coater, air knife coater, transfer roll coater, rod metering size press coater, curtain coater, etc. An on-machine coater or an off-machine coater provided with a processing device can be applied to the base paper in one or more layers. Among these, it is preferable to use a blade coater because high flatness of the coating layer surface is ensured. Moreover, as a drying method in the dryer part, for example, various heating drying methods such as hot air heating, gas heater heating, infrared heater heating and the like can be appropriately employed.
表面層の塗工量は20〜40g/m2とする。なお、この塗工量は、塗工層が1層の場合は、表面層しか存在しないことになるため、塗工層の塗工量と同じである。合成皮革工程紙においては、表面の平坦性(写像性)が低いと、溶媒の液溜まりが発生し易く、溶媒による塗工層の侵食が局所的に発生し、写像性の低下が大きくなる。写像性の低下を防止するために、塗工量は20g/m2以上とする。他方、塗工量が40g/m2を超過すると、乾燥時に塗工層中から蒸発する水蒸気により、塗工層表面に孔が空く、マイクロピットと呼ばれる欠陥が多く発生する。このため、マイクロピットを充分に抑えつつ、写像性を向上させるという観点から、塗工量を20〜40g/m2とする。 The coating amount of the surface layer is set to 20 to 40 g / m 2. This coating amount is the same as the coating amount of the coating layer because there is only a surface layer when there is one coating layer. In the synthetic leather process paper, when the surface flatness (image clarity) is low, the liquid pool of the solvent is likely to occur, the coating layer is eroded locally by the solvent, and the image clarity is greatly deteriorated. In order to prevent a decrease in image clarity, the coating amount is 20 g / m 2 or more. On the other hand, when the coating amount exceeds 40 g / m 2 , holes are formed in the surface of the coating layer due to water vapor evaporated from the coating layer during drying, and many defects called micropits are generated. For this reason, the coating amount is set to 20 to 40 g / m 2 from the viewpoint of improving the image clarity while sufficiently suppressing the micropits.
本形態においては、前述した各種条件(鏡面処理されている、接着剤がポリアクリル酸、ポリビニルアルコール、ポリアクリル酸−ポリビニルアルコール共重合体を含む)を満たす塗工層を、原紙の両方の面に設けることができるが、一方の面のみに設けることもできる。一方の面のみに設ける場合は、他方の面にいかなる処理をするか、何も処理をしないか、などは特に限定されない。もちろん、上記各種条件を満たさない顔料及び接着剤を主成分とする塗工層を設けても良く、また、澱粉あるいは澱粉誘導体、サイズ剤や合成紙力剤などの各種紙用外添塗工薬品を塗工しても良い。このほか、カール防止の点から、水塗工を行うこともできる。 In this embodiment, the coating layers satisfying the various conditions described above (mirror-treated, and the adhesive contains polyacrylic acid, polyvinyl alcohol, polyacrylic acid-polyvinyl alcohol copolymer) are provided on both sides of the base paper. However, it can also be provided on only one surface. In the case of providing only on one surface, there is no particular limitation on what kind of processing is performed on the other surface or whether no processing is performed. Of course, a coating layer mainly composed of pigments and adhesives that do not satisfy the above various conditions may be provided, and various external additive coating agents for paper such as starch or starch derivatives, sizing agents and synthetic paper strength agents. May be applied. In addition, water coating can be performed from the viewpoint of curling prevention.
また、本形態の工程紙は、次記処理を行ったときのJIS H 8686−2に基づいて測定した写像性の低下率が20%以下であるのが好ましく、15%以下であるのがより好ましく、更には10%以下、特に5%以下とするのが好ましい。
(処理)
塗工層表面にメチルエチルケトン(MEK)又はトルエンを1g/m2の塗工量となるようにNo.2のワイヤーバーで塗工し、30秒経過してから90秒間130℃に加熱する。
この形態によると、例えば合成皮革工程紙用途では、製造する合成皮革の鏡面性の低下が少なく、見栄えの良い合成皮革となり好ましい。また、溶剤による劣化が起こり難いことから、トラレなどの欠陥発生が低減でき、剥離性が良好なため効率的に合成皮革の製造ができるなど、繰り返し使用に耐え得る塗工紙となる。他に、紙袋やブックカバー用途においても、汗や風雨による品質劣化が少ない、耐水性に優れた塗工紙となる。
Further, in the process paper of this embodiment, the rate of decrease in image clarity measured based on JIS H 8686-2 when the following processing is performed is preferably 20% or less, and more preferably 15% or less. More preferably, it is 10% or less, particularly 5% or less.
(processing)
The coating layer surface was coated with methyl ethyl ketone (MEK) or toluene so that the coating amount was 1 g / m 2 . 2. Coat with 2 wire bars and heat to 130 ° C. for 90 seconds after 30 seconds.
According to this embodiment, for example, in the use of synthetic leather process paper, it is preferable that the synthetic leather to be manufactured is less deteriorated in mirror surface and has good appearance. Further, since the deterioration due to the solvent is difficult to occur, the occurrence of defects such as trays can be reduced, and the synthetic paper can be efficiently manufactured because of good peelability. Thus, the coated paper can withstand repeated use. In addition, for paper bags and book covers, the coated paper has excellent water resistance with little quality deterioration due to sweat and wind and rain.
かくして得られる本形態の工程紙は、接着剤としてポリアクリル酸とポリビニルアルコール、または、ポリアクリル酸−ポリビニルアルコール共重合体を使用し、JIS P 8119に基づいて測定したベック平滑度が500〜3000秒、好ましくは600〜2000秒、Tappi T536cm−02に基づいて測定した透気度が1000〜3000秒、好ましくは1200〜2000秒である。これにより、極性溶剤接触後の写像性の低下が少ない、耐溶剤性に優れた工程紙、特には、合成皮革工程紙となる。これは、平滑度が500秒未満では、表面が粗いため、溶媒を塗布した際に局所的な溶媒の溜まりが発生しやすく、局所的な写像性の低下が発生し易い。他方、3000秒超では平滑性が十分に高く、これ以上の平坦化を行っても耐溶剤性が頭打ちになるだけで、経済的に好ましくない。透気度が1000秒未満では、塗工面の空隙が多く、溶媒が浸透し易いため、劣化が進みやすい。他方、3000秒超では、平滑度と同様に、透気度が十分に高く、これ以上の耐透気性を施しても耐溶剤性が頭打ちになるだけで、経済的に好ましくない。特に、本形態では、表面層の塗工量を20〜40g/m2の高塗工量にするため、透気度が3000秒を超えると、表面層中の水分が蒸気となって抜けるのが遅くなり、好ましくない。以上の平滑度や透気度の調節方法は特に限定されず、例えば、平坦化を行うためのキャスト仕上げ条件、特に線圧や速度等を調節することで調節することができる。もっとも、キャスト仕上げによる処理は原紙にも影響を与えるため、平滑度や透気度を調節するにあたっても、できる限り弱い処理とするのが好ましい。そこで、これを補うために、表面層の塗工量を25〜35g/m2とするのが好ましい。塗工量が25g/m2以上であれば平滑度(写像性)を向上させ易く、他方、塗工量が35g/m2以下であれば透気度が相対的に下がるためキャスト仕上げによる調整を弱い処理とすることができる。 Thus, the process paper of this form obtained uses polyacrylic acid and polyvinyl alcohol, or a polyacrylic acid-polyvinyl alcohol copolymer as an adhesive agent, and the Beck smoothness measured based on JISP8119 is 500-3000. The air permeability measured based on seconds, preferably 600 to 2000 seconds and Tappi T536 cm-02, is 1000 to 3000 seconds, preferably 1200 to 2000 seconds. As a result, a process paper , particularly a synthetic leather process paper, which has little deterioration in image clarity after contact with a polar solvent and has excellent solvent resistance is obtained. This is because when the smoothness is less than 500 seconds, the surface is rough, and therefore, when the solvent is applied, a local accumulation of solvent is likely to occur, and local image clarity is likely to decrease. On the other hand, if it exceeds 3000 seconds, the smoothness is sufficiently high, and even if flattening beyond this, the solvent resistance only reaches its peak, which is economically undesirable. When the air permeability is less than 1000 seconds, there are many voids on the coated surface, and the solvent easily permeates, so that deterioration easily proceeds. On the other hand, if it exceeds 3000 seconds, the air permeability is sufficiently high as in the case of smoothness, and even if the air resistance higher than this is applied, the solvent resistance will reach its peak, which is not economically preferable. In particular, in this embodiment, in order to make the coating amount of the surface layer 20 to 40 g / m 2 , when the air permeability exceeds 3000 seconds, moisture in the surface layer escapes as vapor. Is slow and is not preferable. The method for adjusting the smoothness or air permeability is not particularly limited, and can be adjusted by adjusting, for example, cast finish conditions for flattening, particularly linear pressure and speed. However, since the treatment by casting finish also affects the base paper, it is preferable to make the treatment as weak as possible when adjusting the smoothness and air permeability. Therefore, in order to compensate for this, the coating amount of the surface layer is preferably 25 to 35 g / m 2 . If the coating amount is 25 g / m 2 or more, it is easy to improve the smoothness (image clarity). On the other hand, if the coating amount is 35 g / m 2 or less, the air permeability is relatively lowered. Can be a weak process.
得られた工程紙には、剥離剤を塗工することで、耐溶剤性と剥離性を向上させることができる。剥離剤としては、剥離紙用途に一般的に用いられている、ポリプロピレン系樹脂、ポリメチルペンテン系樹脂、シリコーン系樹脂、アルキド系樹脂などを使用することができる。ポリプロピレン系樹脂は繰り返しの使用に優れているが、耐熱性が悪く高温での使用に限界があり表面も傷つきやすいという欠点がり、より耐熱性の良好なポリメチルペンテン系樹脂が使用されている。シリコーン系の樹脂は剥離性には優れているが剥離力や光沢のコントロール、塗膜の均一性に難点があり、アルキド系樹脂は耐熱性や光沢のコントロールに優れるが剥離性が乏しいという欠点がある。本形態においては、工程紙の使用条件や要求品質に応じて上記4種類の剥離剤を使い分けることができるが、特に耐熱性が良好なアルキド系樹脂を使用することが好ましい。これら樹脂組成物を原紙へ塗工することにより、本発明の目的である、光沢度、写像性が高く、剥離性が良好であり、見栄えの良い合成皮革を製造できる工程紙が得られる。 Solvent resistance and peelability can be improved by applying a release agent to the obtained process paper . As the release agent, polypropylene resins, polymethylpentene resins, silicone resins, alkyd resins, and the like that are generally used for release paper applications can be used. Polypropylene resins are excellent in repeated use, but have the disadvantages of poor heat resistance and limited use at high temperatures, and the surface is easily damaged, and polymethylpentene resins with better heat resistance are used. Silicone resins are excellent in releasability, but there are drawbacks in peel strength and gloss control, and uniformity of the coating film, and alkyd resins have excellent heat resistance and gloss control but have poor delamination properties. is there. In the present embodiment, the above four types of release agents can be properly used depending on the use conditions and required quality of the process paper , but it is particularly preferable to use an alkyd resin having good heat resistance. By coating these resin compositions into the base paper is an object of the present invention, gloss, high clarity, releasability is good, casting paper can be produced good-looking synthetic leather is obtained.
一方、工程紙の原紙は、通常の原料パルプを使用することができ、例えば、未晒針葉樹パルプ(NUKP)、未晒広葉樹パルプ(LUKP)、晒針葉樹パルプ(NBKP)、晒広葉樹パルプ(LBKP)等の化学パルプ;ストーングランドパルプ(SGP)、加圧ストーングランドパルプ(PGW)、リファイナーグランドパルプ(RGP)、ケミグランドパルプ(CGP)、サーモグランドパルプ(TGP)、グランドパルプ(GP)、サーモメカニカルパルプ(TMP)、ケミサーモメカニカルパルプ(CTMP)、リファイナーメカニカルパルプ(RMP)等の機械パルプ等を使用することができる。また、古紙からなる古紙パルプを使用することも可能であり、例えば、茶古紙、クラフト封筒古紙、雑誌古紙、新聞古紙、チラシ古紙、オフィス古紙、段ボール古紙、上白古紙、ケント古紙、模造古紙、地券古紙等から製造される離解古紙パルプ、離解・脱墨古紙パルプ、離解・脱墨・漂白古紙パルプ等があげられる。本形態では、これらの中から1種又は2種以上を適宜選択して使用することができる。 On the other hand, the raw paper for the process paper can use normal raw pulp, for example, unbleached softwood pulp (NUKP), unbleached hardwood pulp (LUKP), bleached softwood pulp (NBKP), bleached hardwood pulp (LBKP) Chemical pulps such as: Stone Grand Pulp (SGP), Pressurized Stone Grand Pulp (PGW), Refiner Grand Pulp (RGP), Chemi Grand Pulp (CGP), Thermo Grand Pulp (TGP), Grand Pulp (GP), Thermomechanical Mechanical pulp such as pulp (TMP), chemi-thermomechanical pulp (CTMP), refiner mechanical pulp (RMP), and the like can be used. It is also possible to use waste paper pulp made of waste paper, for example, tea waste paper, craft envelope waste paper, magazine waste paper, newspaper waste paper, flyer waste paper, office waste paper, corrugated waste paper, upper white waste paper, Kent waste paper, imitation waste paper, Examples include disaggregated waste paper pulp, disaggregated / deinked waste paper pulp, disaggregated / deinked / bleached waste paper pulp, etc., manufactured from old paper. In this embodiment, one or more of these can be appropriately selected and used.
本形態においては、以上の原料パルプを混合して抄紙原料(紙料スラリー)を調製するが、当該原料パルプには、例えば、内添サイズ剤、紙力増強剤、紙厚向上剤、歩留向上剤等の通常の製紙工程で配合される種々の添加剤を、その種類及び配合量を適宜調整して内添することができる。 In this embodiment, the above raw material pulp is mixed to prepare a papermaking raw material (stock slurry). For the raw material pulp, for example, an internally added sizing agent, a paper strength enhancer, a paper thickness improver, a yield Various additives blended in the normal papermaking process such as an improver can be internally added by appropriately adjusting the kind and blending amount.
また、原紙を抄造する抄紙機も特に限定されず、例えば、長網方式、ツインワイヤー方式、ギャップフォーマー方式、丸網方式、ヤンキー方式など各方式を適宜用いることができる。 Also, the paper machine for making the base paper is not particularly limited, and for example, various systems such as a long net system, a twin wire system, a gap former system, a round net system, and a Yankee system can be appropriately used.
また、本件発明の塗工を行う前に、原紙を平坦化する目的で、前記一般の塗工紙用途設備を用いた塗工や、前記弾性ロールと金属ロールとの組み合わせによる平坦化処理を行う方が好ましい。 Moreover, before performing the coating of the present invention, for the purpose of flattening the base paper, a coating using the general coated paper application facility or a flattening process by a combination of the elastic roll and the metal roll is performed. Is preferred.
次に、実施例を挙げて本発明による作用効果を明らかにするが、本発明はこれら実施例に限定されるものではない。 Next, although an example and an example are given and the operation effect by the present invention is clarified, the present invention is not limited to these examples.
〔原紙〕
原料として広葉樹晒クラフトパルプ100%のパルプを使用し、フリーネスを370mlとした。絶乾パルプ1tに対して、カチオン化澱粉を5kg、サイズ剤0.2kgをそれぞれ有効成分基準で内添し、填料として軽質炭酸カルシウムを灰分10%となるよう内添した。長網抄紙機で抄造・乾燥して原紙を得た。原紙の米坪は117〜142g/m2であり、塗工紙の米坪が157g/m2となるよう、調整した。
〔Base paper〕
100% hardwood bleached kraft pulp was used as a raw material, and the freeness was 370 ml. 5 kg of cationized starch and 0.2 kg of a sizing agent were internally added to the absolutely dry pulp 1 t on the basis of active ingredients, respectively, and light calcium carbonate as a filler was internally added so as to have an ash content of 10%. Paper was obtained by paper making and drying with a long paper machine. The basis weight of the base paper was 117 to 142 g / m 2 , and the coated paper was adjusted so that the basis weight was 157 g / m 2 .
〔塗工層〕
表1に示す種類及び割合の接着剤及び顔料(クレー及び重質炭酸カルシウム)を常温にて混合撹拌して塗工剤を調製し、片面あたり固形分換算で表1の塗工量となるように、20m/分の速度でエアーナイフ塗工し、キャストコート法で仕上げた。なお、用いた顔料及び接着剤は以下のとおりである。また、表1の接着剤の配合量は、顔料100質量部に対する値である。さらに、本例は塗工層が1層であるため、塗工層と表面層が同じである。
・クレー(カオリン、品番:HYDRASPERSE90、HUBER社製)
・重質炭酸カルシウム(湿式、品番:エスカロン#90、三共製粉株式会社製)
・カゼイン(日成共益株式会社製)
・スチレン−ブタジエンラテックス(SBR)(品番:PA5036、日本エイアンドエル株式会社製)
・ポリアクリル酸(PAA)(品番:アクアリックR HL、日本触媒株式会社)
・ポリビニルアルコール(PVA)(型番:PVA405、株式会社クラレ)
・ポリアクリル酸−ポリビニルアルコール共重合体(PAA−PVA)(型番:コーガムHW400、昭和高分子株式会社製)
[Coating layer]
The coating agent is prepared by mixing and stirring the adhesives and pigments (clay and heavy calcium carbonate) of the types and proportions shown in Table 1 at room temperature, so that the coating amount shown in Table 1 is calculated in terms of solid content per side. Then, air knife coating was performed at a speed of 20 m / min, and finished by a cast coating method. The pigments and adhesives used are as follows. Moreover, the compounding quantity of the adhesive agent of Table 1 is a value with respect to 100 mass parts of pigments. Furthermore, since this example has one coating layer, the coating layer and the surface layer are the same.
・ Clay (kaolin, product number: HYDRASPERS90, manufactured by HUBER)
・ Heavy calcium carbonate (wet, product number: ESCALON # 90, manufactured by Sankyo Flour Milling Co., Ltd.)
・ Casein (manufactured by Nissei Kyobun Co., Ltd.)
・ Styrene-butadiene latex (SBR) (Part No .: PA5036, manufactured by Nippon A & L Co., Ltd.)
・ Polyacrylic acid (PAA) (Part No .: Aquaric R HL, Nippon Shokubai Co., Ltd.)
・ Polyvinyl alcohol (PVA) (model number: PVA405, Kuraray Co., Ltd.)
・ Polyacrylic acid-polyvinyl alcohol copolymer (PAA-PVA) (model number: Cogham HW400, Showa Polymer Co., Ltd.)
〔剥離層〕
合成樹脂100質量部に対し、触媒6質量部、トルエン40質量部を混合して剥離剤液を調製した。次いで、剥離剤を片面あたり10g/m2の塗工量となるようNo.2ワイヤーバーで塗工した後、170℃に1分間加熱して硬化させ、剥離層を形成した。用いた塗工紙の種類を表2に示した。なお、用いた薬品は次のとおりである。
合成樹脂:アルキッド樹脂(品番:テスファイン303、日立化成ポリマー(株)製)
触媒(品番:ドライヤー900、日立化成ポリマー(株)製)
トルエン(品番:特級、和光純薬工業(株)製)
[Peeling layer]
A release agent solution was prepared by mixing 6 parts by mass of the catalyst and 40 parts by mass of toluene with respect to 100 parts by mass of the synthetic resin. Subsequently, No. 1 was applied so that the release agent had a coating amount of 10 g / m 2 per side. After coating with a 2 wire bar, it was cured by heating at 170 ° C. for 1 minute to form a release layer. Table 2 shows the types of coated paper used. The chemicals used are as follows.
Synthetic resin: Alkyd resin (Part No .: Tesfine 303, manufactured by Hitachi Chemical Co., Ltd.)
Catalyst (Product No .: Dryer 900, manufactured by Hitachi Chemical Polymer Co., Ltd.)
Toluene (Product number: Special grade, Wako Pure Chemical Industries, Ltd.)
〔比較例〕
接着剤の成分と塗工量等を、表1に示すとおり変化させて比較例とした。
[Comparative Example]
The composition of the adhesive, the coating amount, and the like were changed as shown in Table 1 to make a comparative example.
〔評価方法〕
以上のようにして製造した各種塗工紙について、以下のとおり測定・評価を行った。
1)ベック平滑度
JIS P 8119に準じて測定した。
〔Evaluation methods〕
The various coated papers produced as described above were measured and evaluated as follows.
1) Beck smoothness Measured according to JIS P 8119.
2)透気度
Tappi T536cm−02に準じて測定した。
2) Air permeability Measured according to Tappi T536cm-02.
3)マイクロピット
表面層を目視及びルーペ(10倍)で観察し、発生したマイクロピットを次の基準で評価した。
◎:マイクロピットが発生せず、良好であった。
○:マイクロピットが若干、発生したが、良好であった。
△:マイクロピットが多少、発生したが、実使用に問題ない程度であった。
×:マイクロピットが発生し、実使用できない程度であった。
3) Micropits The surface layer was observed visually and with a magnifying glass (10 times), and the generated micropits were evaluated according to the following criteria.
(Double-circle): The micropit did not generate | occur | produce but was favorable.
◯: Some micropits were generated but were good.
Δ: Some micropits were generated, but there was no problem in actual use.
X: Micro pits were generated and were not practically usable.
4)耐溶剤性試験
前記塗工紙(幅100×縦148mm)の塗工層表面にメチルエチルケトン(MEK)又はトルエンを1g/m2の塗工量となるようにNo.2のワイヤーバーで塗工し、30秒経過してから90秒間130℃に加熱した。この処理を行う前後の写像性を測定した。写像性は、JIS H 8686−2に準じて測定した。また、変化率は、次の式で算出した。
変化率(%)=(1−(試験後の測定値/試験前の測定値))×100
4) Solvent resistance test No. 1 was applied so that methyl ethyl ketone (MEK) or toluene was applied at a coating amount of 1 g / m 2 on the surface of the coating layer of the coated paper (width 100 × length 148 mm). The coating was performed with a wire bar No. 2, and after 30 seconds, it was heated to 130 ° C. for 90 seconds. The image clarity before and after this treatment was measured. The image clarity was measured according to JIS H 8686-2. The rate of change was calculated by the following formula.
Rate of change (%) = (1− (measured value after test / measured value before test)) × 100
5)耐剥離性
剥離紙上に、ポリ塩化ビニル100質量部、ジオクチルフタレート50質量部、発泡剤5部、安定剤3部を混合して得られたポリ塩化ビニルゾルを、No.2ワイヤーバーを用いて塗工量が30g/m2になるように塗工した。その後、200℃で3分間、加熱硬化させて発泡ポリ塩化ビニルシート層を形成し、これを剥離紙から剥離した。この作業を10回繰り返した後に、剥離紙表面を目視で次のとおり評価した。
◎:塗工層と剥離層がポリ塩化ビニルシートに剥ぎ取られず、良好であった。
○:塗工層と剥離層がポリ塩化ビニルシートに若干剥ぎ取られ、耐剥離性に若干劣る。
×:塗工層と剥離層がポリ塩化ビニルシートに多く剥ぎ取られ、耐剥離性に劣る。
なお、◎及び○が実使用に問題ないレベルである。また、用いた薬品は次のとおりである。
ポリ塩化ビニル(品番:ゼオン121、日本ゼオン(株)製)
ジオクチルフタレート(シージーエスター(株)製)
発泡剤(アゾジカルボンアミド、永和化成工業(株)製)
安定剤(品番:BZ−100CJ、勝田化工(株)製)
5) Peel resistance Polyvinyl chloride sol obtained by mixing 100 parts by mass of polyvinyl chloride, 50 parts by mass of dioctyl phthalate, 5 parts of foaming agent, and 3 parts of stabilizer on release paper was obtained as It applied so that the coating amount might be 30 g / m < 2 > using 2 wire bars. Then, it was heat-cured at 200 ° C. for 3 minutes to form a foamed polyvinyl chloride sheet layer, which was peeled from the release paper. After repeating this operation 10 times, the release paper surface was visually evaluated as follows.
(Double-circle): The coating layer and the peeling layer were not peeled off by the polyvinyl chloride sheet, and were favorable.
A: The coating layer and the release layer are slightly peeled off to the polyvinyl chloride sheet, and the peel resistance is slightly inferior.
X: Many coating layers and peeling layers are peeled off by the polyvinyl chloride sheet, and it is inferior to peeling resistance.
In addition, (double-circle) and (circle) are a level which does not have a problem in actual use. The chemicals used are as follows.
Polyvinyl chloride (Part No .: ZEON 121, manufactured by ZEON CORPORATION)
Dioctyl phthalate (manufactured by CG Esther)
Foaming agent (azodicarbonamide, manufactured by Eiwa Kasei Kogyo Co., Ltd.)
Stabilizer (Product No .: BZ-100CJ, manufactured by Katsuta Chemical Corporation)
表1及び表2に、以上の試験による結果を示した。表1に示すように、実施例では、メチルエチルケトン又はトルエンを用いた耐溶剤性試験による写像性の変化率が20%以下であり、極性溶剤に対する耐性が優れ、マイクロピットの発生が少ない。他方、接着剤として、ポリアクリル酸及びポリビニルアルコール、並びに、ポリアクリル酸−ポリビニルアルコール共重合体を配合しないか、または塗工量が所定の範囲内でない比較例は、メチルエチルケトンまたはトルエンを用いた耐溶剤性試験による写像性の変化率が20%を超過し、極性溶剤に対する耐性が劣るか、マイクロピットの発生が多い。 Tables 1 and 2 show the results of the above tests. As shown in Table 1, in the examples, the rate of change in image clarity by a solvent resistance test using methyl ethyl ketone or toluene is 20% or less, the resistance to polar solvents is excellent, and the generation of micropits is small. On the other hand, as a comparative example in which polyacrylic acid and polyvinyl alcohol, and polyacrylic acid-polyvinyl alcohol copolymer are not blended or the coating amount is not within a predetermined range, a resistance value using methyl ethyl ketone or toluene is used. The rate of change in image clarity by the solvent test exceeds 20%, and the resistance to polar solvents is poor or micropits are frequently generated.
表2に示すように、実施例は、接着剤として、ポリアクリル酸及びポリビニルアルコール、並びに、ポリアクリル酸−ポリビニルアルコール共重合体を配合し、塗工量を所定の範囲内とした塗工紙上に剥離層を設けたため、耐剥離性が良好であった。他方、接着剤として、ポリアクリル酸及びポリビニルアルコール、並びに、ポリアクリル酸−ポリビニルアルコール共重合体を配合しなかった塗工紙、あるいは、塗工量が所定の範囲内でない塗工紙の上に、剥離層を設けた比較例は、耐剥離性が悪く、実使用に耐えない塗工紙となった。 As shown in Table 2, in Examples, on the coated paper, polyacrylic acid and polyvinyl alcohol, and polyacrylic acid-polyvinyl alcohol copolymer were blended as adhesives, and the coating amount was within a predetermined range. Since the release layer was provided on the surface, the peel resistance was good. On the other hand, on the coated paper not blended with polyacrylic acid and polyvinyl alcohol and polyacrylic acid-polyvinyl alcohol copolymer as an adhesive, or on coated paper whose coating amount is not within a predetermined range. The comparative example provided with a release layer was poor in peel resistance and became a coated paper that could not withstand actual use.
本発明は、有機溶剤を用いて製造する合成皮革の工程紙などとして利用するに好適な工程紙として、適用可能である。 The present invention can be applied as a process paper suitable for use as a process paper for synthetic leather produced using an organic solvent.
Claims (8)
前記接着剤が、ポリアクリル酸及びポリビニルアルコールの両方を合計配合量が前記顔料100質量部に対して1〜20質量部となるように含み、
前記顔料が、クレーを当該顔料100質量部に対して20〜80質量部含み、
前記塗工層の表面層が、塗工量20〜40g/m2とされ、かつキャストコート法で鏡面処理されている、
ことを特徴とする工程紙。 And base paper, a process paper having a least one layer of the coating layer composed mainly pigment and an adhesive provided on at least one surface of the base paper,
The adhesive contains both polyacrylic acid and polyvinyl alcohol so that the total blending amount is 1 to 20 parts by mass with respect to 100 parts by mass of the pigment ,
The pigment contains 20 to 80 parts by mass of clay with respect to 100 parts by mass of the pigment;
The surface layer of the coating layer has a coating amount of 20 to 40 g / m 2 and is mirror-finished by a cast coating method.
Process paper characterized by that .
請求項1記載の工程紙。The process paper according to claim 1.
請求項1又は請求項2記載の工程紙。The process paper according to claim 1 or 2.
請求項1〜3のいずれか1項に記載の工程紙。The process paper of any one of Claims 1-3.
請求項1〜4のいずれか1項に記載の工程紙。 The polyacrylic acid and polyvinyl alcohol contained in the adhesive have a molar ratio of 10:90 to 90:10 (a total molar amount including both a monomer and a copolymer). Ratio) ,
The process paper of any one of Claims 1-4 .
JIS P 8119に基づいて測定したベック平滑度が500〜3000秒、Tappi T536cm−02に基づいて測定した透気度が1000〜3000秒とされている、
請求項1〜5のいずれか1項に記載の工程紙。 The surface layer of the coating layer has a coating amount of 25 to 35 g / m 2 ,
The Beck smoothness measured based on JIS P 8119 is 500 to 3000 seconds, and the air permeability measured based on Tappi T536cm-02 is 1000 to 3000 seconds.
The process paper of any one of Claims 1-5 .
請求項1〜6のいずれか1項に記載の工程紙。
(処理)
前記塗工層表面にメチルエチルケトン(MEK)又はトルエンを1g/m2の塗工量となるようにNo.2のワイヤーバーで塗工し、30秒経過してから90秒間130℃に加熱する。 The rate of decrease in image clarity measured based on JIS H 8686-2 when the following processing is performed is 20% or less.
The process paper of any one of Claims 1-6 .
(processing)
The coating layer surface was coated with methyl ethyl ketone (MEK) or toluene so that the coating amount was 1 g / m 2 . 2. Coat with 2 wire bars and heat to 130 ° C. for 90 seconds after 30 seconds.
請求項1〜7のいずれか1項に記載の工程紙。 A release layer was provided by applying a release agent on the coating layer,
Step paper according to any one of claims 1-7.
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