JP2011038227A - Coated wrapping paper - Google Patents
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- JP2011038227A JP2011038227A JP2009188832A JP2009188832A JP2011038227A JP 2011038227 A JP2011038227 A JP 2011038227A JP 2009188832 A JP2009188832 A JP 2009188832A JP 2009188832 A JP2009188832 A JP 2009188832A JP 2011038227 A JP2011038227 A JP 2011038227A
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- 239000000123 paper Substances 0.000 claims abstract description 83
- 239000000049 pigment Substances 0.000 claims abstract description 34
- 239000005995 Aluminium silicate Substances 0.000 claims abstract description 31
- 235000012211 aluminium silicate Nutrition 0.000 claims abstract description 31
- 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 31
- 239000000853 adhesive Substances 0.000 claims abstract description 20
- 230000001070 adhesive effect Effects 0.000 claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000002655 kraft paper Substances 0.000 claims abstract description 14
- 238000010521 absorption reaction Methods 0.000 claims abstract description 13
- 229920000881 Modified starch Polymers 0.000 claims abstract description 9
- 235000019426 modified starch Nutrition 0.000 claims abstract description 9
- 239000011247 coating layer Substances 0.000 claims description 17
- 238000004806 packaging method and process Methods 0.000 claims description 17
- 239000000454 talc Substances 0.000 claims description 12
- 229910052623 talc Inorganic materials 0.000 claims description 12
- 238000007639 printing Methods 0.000 abstract description 34
- 238000011161 development Methods 0.000 abstract description 10
- 238000001035 drying Methods 0.000 abstract description 5
- 239000000976 ink Substances 0.000 description 57
- 239000011248 coating agent Substances 0.000 description 19
- 238000000576 coating method Methods 0.000 description 19
- 239000003973 paint Substances 0.000 description 18
- 239000002585 base Substances 0.000 description 16
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 12
- 229920000126 latex Polymers 0.000 description 10
- 239000004816 latex Substances 0.000 description 10
- 239000001254 oxidized starch Substances 0.000 description 10
- 235000013808 oxidized starch Nutrition 0.000 description 10
- 229920002472 Starch Polymers 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000010893 paper waste Substances 0.000 description 8
- 235000019698 starch Nutrition 0.000 description 8
- 239000008107 starch Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 229910000019 calcium carbonate Inorganic materials 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- -1 satin white Chemical compound 0.000 description 4
- 206010016807 Fluid retention Diseases 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 229920001131 Pulp (paper) Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229910001919 chlorite Inorganic materials 0.000 description 3
- 229910052619 chlorite group Inorganic materials 0.000 description 3
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000007646 gravure printing Methods 0.000 description 3
- 239000011121 hardwood Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000007645 offset printing Methods 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000011122 softwood Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 229920002261 Corn starch Polymers 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 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
- 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
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 229940099112 cornstarch Drugs 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000013054 paper strength agent Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000009182 swimming Effects 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 241000218631 Coniferophyta Species 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 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
- 238000007774 anilox coating Methods 0.000 description 1
- 238000004061 bleaching 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
- 238000003490 calendering Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 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
- 239000010897 cardboard waste Substances 0.000 description 1
- 229920006319 cationized starch Polymers 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000013055 pulp slurry Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Paper (AREA)
Abstract
Description
本発明はフレキソ印刷適性に優れ、製袋適性を備えた塗工包装用紙に関する。 The present invention relates to a coated and wrapping paper having excellent flexographic printing suitability and bag making suitability.
近年、印刷物の多色化が進み、要求される印刷品質の高級化、印刷速度の高速化が進んできており、それに対応する包装用紙の開発が求められている。ショッピングバックに代表されるような紙製手提げ袋に用いられる包装用紙においても、印刷品質の高級化が強く要求されている。印刷品質の高級化手法としては、例えば、高速で高精細なオフセット印刷やグラビア印刷での印刷が一般的である。しかしながら、包装用紙においては、フレキソ印刷の使用状況はいまだに多く、その印刷品質は、オフセット印刷やグラビア印刷に比べて見劣り感がすることは否めない。一方、フレキソ印刷の技術進歩も目覚しく、小ロット多品種化や環境と安全性問題、コスト削減などの市場課題に対して、近年のデジタル化の波とともに、画期的で斬新な技術でもって注目されている。さらに印刷品質についても、他の印刷方式と比較しても遜色ないレベルまで改良されている。フレキソ印刷は上述のごとく、水性化や無溶剤化の面で大きな優位性が認められ、欧米の包装分野では既にフレキソ印刷が主流となっており、日本においても普及の兆しがある。このようなフレキソ技術を駆使して、一般に使用されているオフセット用やグラビア用印刷用紙にフレキソ印刷をしても、インキ発色性が劣るので濃度の高い印刷ができず、多量にインキを載せると、画線部のインキが紙に吸着せず、流れる現象がおき、印刷品質を高級化するには不十分であった。 In recent years, the number of colors of printed materials has been increasing, so that the required printing quality has been improved and the printing speed has been increased, and the development of packaging paper corresponding to these has been required. There is also a strong demand for higher printing quality in packaging paper used for paper handbags such as shopping bags. As a technique for improving the print quality, for example, printing by high-speed and high-definition offset printing or gravure printing is generally used. However, in the case of wrapping paper, flexo printing is still used in many situations, and it cannot be denied that its print quality is inferior to that of offset printing or gravure printing. On the other hand, flexographic printing technology has also made remarkable progress, and with the recent wave of digitization, attention has been paid to innovative and innovative technologies against market issues such as multi-lot production, environmental and safety issues, and cost reductions. Has been. Furthermore, the print quality has also been improved to a level comparable to other printing methods. As described above, flexographic printing has a great advantage in terms of water-based and solvent-free printing. Flexographic printing has already become mainstream in the packaging field in Europe and the United States, and there are signs of widespread use in Japan. Even if flexographic printing is performed on commonly used offset or gravure printing paper by using such flexographic technology, it is inferior in ink color development and cannot be printed with high density. However, the ink in the image area does not adsorb to the paper and flows, which is insufficient for improving the printing quality.
また、包装用紙は、品物を包装、保持する役割が必要なため、印刷品質だけでなく、強度、剛度などの品質も重要な要素のひとつである。印刷品質と強度を両立する手法として例えば、原紙に両性ポリアクリルアミド系紙力剤及びポリアミドエピクロロヒドリン系紙力剤を含有させ、湿潤強度を持たせた原紙の片面にピグメント層を形成することが例示されている(特許文献1)。 In addition, since the packaging paper needs to have a role of packaging and holding the goods, not only the printing quality but also the quality such as strength and rigidity is one of the important factors. As a technique for achieving both printing quality and strength, for example, an amphoteric polyacrylamide paper strength agent and a polyamide epichlorohydrin paper strength agent are contained in the base paper, and a pigment layer is formed on one side of the base paper with wet strength. Is exemplified (Patent Document 1).
原紙抄紙時に表裏の繊維配向角の差、及び繊維配向比をある範囲に調整し、少なくとも一方の面に1〜10g/m2の塗工層を設けることが提示されている(特許文献2)。 It has been proposed that the fiber orientation angle difference between the front and back sides and the fiber orientation ratio are adjusted to a certain range during base paper making, and a coating layer of 1 to 10 g / m 2 is provided on at least one surface (Patent Document 2). .
また、針葉樹クラフトパルプを50重量%以上用いて形成され、縦横引っ張り強度比が1.7以上に調整された原紙上の少なくとも片面に顔料と接着剤とを含有する塗工層が1〜10g/m2形成された坪量が100〜500g/m2の範囲の塗工包装用紙が提示されている(特許文献3)。前記特許文献はいずれもフレキソ印刷を想定しているものではない。 In addition, a coating layer containing a pigment and an adhesive on at least one side of a base paper which is formed using 50% by weight or more of softwood kraft pulp and whose longitudinal / lateral tensile strength ratio is adjusted to 1.7 or more is 1 to 10 g / A coated packaging paper having a basis weight of m 2 formed in the range of 100 to 500 g / m 2 is proposed (Patent Document 3). None of the patent documents assume flexographic printing.
本発明は、フレキソ印刷時におけるフレキソインキ発色性、インキ乾燥性に優れ、かつ、通常製袋機械による操業性に優れた塗工包装用紙を提供するものである。 The present invention provides a coated and wrapping paper that is excellent in flexo ink color development and ink drying properties during flexographic printing, and is excellent in operability by a normal bag making machine.
本発明は原紙の少なくとも片面に顔料と接着剤を含有する塗工層を有する塗工包装用紙において、前記原紙に晒、未晒、半晒クラフトパルプを少なくとも1種を含有し、前記塗工層中の顔料100質量部あたり、焼成カオリンが30〜100質量部、かつ澱粉誘導体が8〜40質量部含有し、さらに塗工面のJAPAN TAPPI No.51による水に対する吸収係数Kaが0.16〜0.35ml/m2・ms1/2の範囲にあることを特徴とする塗工包装用紙である。
前記顔料100質量部に対し、タルクが70質量部以下を含有することが好ましい。
前記顔料100質量部に対し、水分散性接着剤が8〜30質量部を含有するとさらに好ましい。
The present invention provides a coated wrapping paper having a coating layer containing a pigment and an adhesive on at least one side of a base paper, the base paper containing at least one bleached, unbleached, and semi-bleached kraft pulp, and the coating layer 30-100 parts by mass of calcined kaolin and 8-40 parts by mass of starch derivative are contained per 100 parts by mass of the pigment in the pigment, and the coating surface of JAPAN TAPPI No. The coated packaging paper is characterized in that the absorption coefficient Ka with respect to water by 51 is in the range of 0.16 to 0.35 ml / m 2 · ms 1/2 .
It is preferable that talc contains 70 parts by mass or less with respect to 100 parts by mass of the pigment.
More preferably, the water-dispersible adhesive contains 8 to 30 parts by mass with respect to 100 parts by mass of the pigment.
本発明によって、フレキソ印刷におけるインキ発色性に優れた塗工包装用紙を提供することが可能になった。 According to the present invention, it has become possible to provide a coated and wrapping paper excellent in ink color development in flexographic printing.
一般に、フレキソ印刷は水性タイプのインキを使用して印刷が実施されることから、印刷面の吸水性度合いによりインキの浸み込みが異なる。このため、フレキソインキにおけるインキ発色性、および網点再現性は、印刷面の吸水性の度合いとフレキソインキの量に大いに影響される。 In general, flexographic printing is performed using a water-type ink, so that the ink penetration varies depending on the degree of water absorption of the printed surface. For this reason, the ink coloring property and the halftone dot reproducibility in flexographic ink are greatly influenced by the degree of water absorption on the printed surface and the amount of flexographic ink.
フレキソインキは上述のごとく水性タイプのインキであることから、塗工面のJAPAN TAPPI No.51による水に対する吸収係数Kaが0.16〜0.35ml/m2・ms1/2の範囲であると、フレキソ印刷時にインキが速やかに浸透するが、浸透しすぎず、フレキソ印刷に特有なマージナルマークの発生がし難く、優れた印刷品質が得られる。好ましくは吸収係数Kaが0.20〜0.35ml/m2・ms1/2の範囲である。なお、吸収係数Kaが0.16ml/m2・ms1/2未満であると、インキの吸収性が劣ることから、乾燥性が劣り、一般にいう「インキの泳ぎ」の状態になり、余ったフレキソインキが表面に残り不均一に広がることにより不均一な印刷面となる。また、吸収係数Kaが0.35ml/m2・ms1/2を超えると、インキの吸水性は優れるが、その分インキが表面に留まらず、表面から紙層中に浸透してしまい、表面に留まるインキが少なくなるので容易に乾燥するが、インキの発色性が劣り、結果的に色味が異なってしまうことになり、色調整が困難になる。 Since flexographic ink is a water-based ink as described above, the JAPAN TAPPI No. When the absorption coefficient Ka to water by 51 is in the range of 0.16 to 0.35 ml / m 2 · ms 1/2 , the ink penetrates quickly during flexographic printing, but does not penetrate too much and is unique to flexographic printing. Marginal marks are unlikely to occur and excellent print quality can be obtained. The absorption coefficient Ka is preferably in the range of 0.20 to 0.35 ml / m 2 · ms 1/2 . In addition, when the absorption coefficient Ka is less than 0.16 ml / m 2 · ms 1/2 , the ink absorbability is inferior, so that the drying property is inferior, and the state of “ink swimming” is generally reached, and the remainder The flexographic ink remains on the surface and spreads unevenly, resulting in a non-uniform printed surface. Further, when the absorption coefficient Ka exceeds 0.35 ml / m 2 · ms 1/2 , the water absorption of the ink is excellent, but the ink does not stay on the surface, and permeates into the paper layer from the surface. However, the ink stays in the ink and is easily dried. However, the color developability of the ink is inferior, and as a result, the color becomes different, making it difficult to adjust the color.
さらに吸収係数Kaが0.16〜0.35ml/m2・ms1/2の範囲の場合、塗工面の水による動的接触角の低下角度が0.1秒〜1秒範囲の単位時間あたり−3.5〜−0.3度/秒の範囲が好ましく、この範囲であると、印刷時にインキが版の周りに流れ込むことによって生じるマージナルマークの発生がしにくくなる。 Further, when the absorption coefficient Ka is in the range of 0.16 to 0.35 ml / m 2 · ms 1/2 , the decreasing angle of the dynamic contact angle due to the water on the coated surface is per unit time in the range of 0.1 second to 1 second. A range of −3.5 to −0.3 degrees / second is preferable, and when it is within this range, it is difficult to generate a marginal mark caused by ink flowing around the plate during printing.
上記のような特性を得るためには、包装用紙表面に形成する塗工層中に焼成カオリンが必要である。焼成カオリンが塗工層中に存在するとフレキソインキ吸収性が極めてよくなり、この焼成カオリンは塗工層中の顔料として30〜100質量部含有する。好ましくは40〜90質量部、さらに好ましくは50〜80質量部含有する。焼成カオリン及びその他の顔料の配合量を調整することにより、各種のフレキソ印刷機に適応したインキ発色性の優れた品質を得ることができる。 In order to obtain the above characteristics, calcined kaolin is required in the coating layer formed on the surface of the packaging paper. When the calcined kaolin is present in the coating layer, the flexographic ink absorbability is extremely improved, and the calcined kaolin is contained in an amount of 30 to 100 parts by mass as a pigment in the coating layer. Preferably it contains 40-90 mass parts, More preferably, it contains 50-80 mass parts. By adjusting the blending amounts of the calcined kaolin and other pigments, it is possible to obtain a quality with excellent ink color development suitable for various flexographic printing machines.
焼成カオリンを塗工層中に含有するとフレキソ印刷適性を改善する理由は必ずしも定かではないが、焼成カオリンは、天然に産するカオリンをキルンなどで約800℃程度の高温処理することにより、カオリンの結晶構造中に存在する結晶水を放出させたもので、結晶構造が崩壊して非晶質な構造となり、不透明性、多孔質でインキ吸収性に優れた性質を持っている。このことから、焼成カオリンのもつ空隙性によって、顔料中にインキを取り込み、またインキ中の溶剤が均一に吸収されて、インキの発色性と均一性が得られ、また密着性の向上による網点の再現性も得られるものと考える。 The reason why the calcined kaolin is contained in the coating layer to improve the flexibility of flexographic printing is not necessarily clear. However, the calcined kaolin is produced by treating kaolin produced in nature with a kiln or the like at a high temperature of about 800 ° C. The crystal water that is present in the crystal structure is released, the crystal structure is collapsed to become an amorphous structure, and it is opaque, porous, and has excellent ink absorbability. From this, the porosity of the calcined kaolin allows the ink to be taken into the pigment, and the solvent in the ink is absorbed uniformly, resulting in ink color development and uniformity, and a halftone dot due to improved adhesion. It is considered that reproducibility can be obtained.
本発明に使用する焼成カオリン以外の顔料としては、製紙分野で通常使用されている顔料、例えば、クレー、構造化カオリン、エンジニアードカオリン、タルク、水酸化アルミニウム、二酸化チタン、軽質炭酸カルシウム、重質炭酸カルシウム、硫酸バリウム、酸化亜鉛、サチンホワイト、硫酸カルシウム等の一種または二種以上を使用することができる。この中でも、タルクを配合することが好ましい。後加工、製袋加工時に塗工表面に異物が接触して擦れた時、異物付着による汚れが発生しやすいことに対して、タルクが扁平顔料で、塗工層に存在すると摩擦抵抗を低減させる性質を有していることから、異物による汚れを軽減させることが出来る。一般的に製紙用のタルクは、セディグラフによって測定した平均粒径が1〜5μm、クロライト含有率は0〜90%であるが、中でもクロライト含有率5〜80%のタルクの使用は、顔料の分散性と加工時の汚れを軽減させる効果のバランスがとれているため、より好ましい。また、タルク配合部数は顔料100質量部当たり、70質量部以下が好ましい。5質量部以上を含有するとその効果が顕著に発現される。クロライト含有率によりタルク配合部数は変わるものの、さらに好ましくは15〜60質量部である。なお、焼成カオリンを除く顔料は、フレキソインキの吸収性の観点から、本発明の所望する効果を阻害しない範囲で使用するのが望ましいが、プラスチックピグメント等の有機顔料はインキ吸収性が劣るので好ましくない。 Examples of pigments other than calcined kaolin used in the present invention include pigments commonly used in the papermaking field, such as clay, structured kaolin, engineered kaolin, talc, aluminum hydroxide, titanium dioxide, light calcium carbonate, heavy One or more of calcium carbonate, barium sulfate, zinc oxide, satin white, calcium sulfate and the like can be used. Among these, it is preferable to mix talc. When foreign material comes into contact with the coating surface and is rubbed during post-processing or bag-making processing, dirt due to adhesion of foreign material is likely to occur, whereas talc is a flat pigment that reduces frictional resistance when present in the coating layer. Since it has properties, it is possible to reduce contamination due to foreign matter. Generally, talc for papermaking has an average particle size of 1 to 5 μm measured by sedigraph and a chlorite content of 0 to 90%. Among them, the use of talc with a chlorite content of 5 to 80% is This is more preferable because the balance between the dispersibility of the pigment and the effect of reducing dirt during processing is balanced. The number of talc blending parts is preferably 70 parts by mass or less per 100 parts by mass of the pigment. If it contains 5 parts by mass or more, the effect is remarkably exhibited. Although the talc content varies depending on the chlorite content, it is more preferably 15 to 60 parts by mass. In addition, it is desirable to use pigments other than calcined kaolin in a range that does not impair the desired effect of the present invention from the viewpoint of the absorbability of flexographic inks. However, organic pigments such as plastic pigments are preferable because they have poor ink absorbability. Absent.
インキ発色性向上に対して効果を阻害しない範囲において、本発明使用される塗料中に、防滑剤、染料等の添加剤を併用してもよい。 To the extent that the effect on ink color development is not impaired, additives such as anti-slip agents and dyes may be used in combination in the paint used in the present invention.
焼成カオリンは塗料の保水性が著しく低下させることが知られている。塗料保水性が低いと、原紙中に塗料が浸透し易くなり、均一な塗工層が原紙表面に形成することが困難となる。また、塗工装置によっては、塗工筋が発生したり、全く塗工が出来なくなったりすることがあるので、澱粉誘導体を使用することが有効である。 It is known that calcined kaolin significantly reduces the water retention of the paint. If the paint water retention is low, the paint is likely to penetrate into the base paper, and it becomes difficult to form a uniform coating layer on the base paper surface. In addition, depending on the coating apparatus, coating stripes may be generated or coating may not be performed at all, so it is effective to use a starch derivative.
本発明で使用される澱粉誘導体としては、例えば、酸化澱粉、エステル化澱粉、エーテル化澱粉、デキストリン、冷水可溶性澱粉などが挙げられる。その配合量としては、顔料100質量部あたり8〜40質量部が必要であり、10〜30質量部がより好ましい。因みに、澱粉誘導体の配合量が8質量部未満であると、塗料としての保水性に劣り、塗料が原紙中に浸透しやすくなって、均一な塗工皮膜ができなくなることにより、フレキソインキ発色性が不均一になる恐れがある。澱粉配合量が40質量部を超えると、塗工層全体に対して澱粉量が多くなって、相対的に顔料の割合が低くなり、フレキソインキ吸収性に劣り、インキが塗工層表面に流れてしまう現象が起こってしまう。即ち、焼成カオリンを含有する顔料100質量部あたり澱粉誘導体を8〜40質量部配合することによって、フレキソインキに対する吸収性を阻害することなく、極めて均一な塗工皮膜が得られ、かつ本発明の吸収係数の範囲を実現する。結果としてマージナルマークの発生が抑えられ、高品質の印刷が可能になった。 Examples of the starch derivative used in the present invention include oxidized starch, esterified starch, etherified starch, dextrin, and cold water-soluble starch. As the compounding quantity, 8-40 mass parts per 100 mass parts of pigments are required, and 10-30 mass parts is more preferable. Incidentally, if the amount of the starch derivative is less than 8 parts by mass, the water retention property of the paint is inferior, the paint easily penetrates into the base paper, and a uniform coating film cannot be formed. May become uneven. When the amount of starch exceeds 40 parts by mass, the amount of starch increases with respect to the entire coating layer, the proportion of the pigment becomes relatively low, the flexo ink absorbability is inferior, and the ink flows to the surface of the coating layer. Will happen. That is, by blending 8 to 40 parts by mass of the starch derivative per 100 parts by mass of the pigment containing calcined kaolin, an extremely uniform coating film can be obtained without impairing the absorbability with respect to the flexographic ink, and Realize the range of absorption coefficient. As a result, the occurrence of marginal marks was suppressed and high-quality printing became possible.
本発明に使用される澱粉誘導体以外の接着剤としては、一般の塗被紙製造分野で使用されている公知の接着剤が適宜使用される。例えば、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、スチレンーメチルメタクリレートーブタジエン共重合体ラテックス等の共役ジエン系共重合体ラテックス、アクリル酸エステルおよび/またはメタクリル酸エステルの重合体または共重合体ラテックス等のアクリル系重合体ラテックス、エチレン−酢酸ビニル重合体ラテックス等のビニル系重合体ラテックス、あるいはこれらの各種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重合体または共重合体ラテックス等の水分散性接着剤等が使用でき、1種または2種以上を適宜選択して使用できる。なお、例示した水分散性接着剤の中で、費用と接着強度のバランスの良い、スチレン−ブタジエン共重合体ラテックスを使用することがより好ましい。また、水分散性接着剤の塗工層中の配合量としては、顔料100質量部に対して8〜30質量部が好ましく、さらに好ましくは、10〜25質量部である。これは、焼成カオリンが上述のごとく、多孔質な特徴があることから、塗工層の強度を十分に発現させるに足る範囲である。 As the adhesive other than the starch derivative used in the present invention, a known adhesive used in a general coated paper manufacturing field is appropriately used. For example, styrene-butadiene copolymer latex, methyl methacrylate-butadiene copolymer latex, conjugated diene copolymer latex such as styrene-methyl methacrylate-butadiene copolymer latex, acrylic ester and / or methacrylate ester Acrylic polymer latex such as a polymer or copolymer latex, vinyl polymer latex such as ethylene-vinyl acetate polymer latex, or these various polymer latexes were modified with a functional group-containing monomer such as a carboxyl group. A water-dispersible adhesive such as a polymer or copolymer latex can be used, and one or two or more can be appropriately selected and used. In the exemplified water dispersible adhesive, it is more preferable to use a styrene-butadiene copolymer latex having a good balance between cost and adhesive strength. Moreover, as a compounding quantity in the coating layer of a water dispersible adhesive agent, 8-30 mass parts is preferable with respect to 100 mass parts of pigments, More preferably, it is 10-25 mass parts. This is a range sufficient to sufficiently develop the strength of the coating layer since the fired kaolin has a porous characteristic as described above.
本発明の澱粉誘導体、水分散性接着剤以外で使用できる接着剤としては、ポリビニルアルコール、カルボキシメチルセルロース等が例示される。 Examples of the adhesive that can be used other than the starch derivative and the water-dispersible adhesive of the present invention include polyvinyl alcohol and carboxymethyl cellulose.
本発明の塗工層は、単層であっても、複層であっても差し支えないが、全体の塗工量は0.5〜10g/m2が好ましい。塗工量がこの範囲であると、経済性にすぐれ、且つ水性フレキソのインキ発色性が優れた塗工包装用紙が得られる。より好ましい塗工量としては、1.5〜7.5g/m2である。 The coating layer of the present invention may be a single layer or a multilayer, but the total coating amount is preferably 0.5 to 10 g / m 2 . When the coating amount is within this range, it is possible to obtain a coated and wrapping paper that is excellent in economic efficiency and excellent in water-colored flexographic ink color development. A more preferable coating amount is 1.5 to 7.5 g / m 2 .
本発明の塗料を原紙に塗工するに当たっては、塗被紙製造に一般に使用される塗工装置が使用でき、例えば、ブレードコーター、エアーナイフコーター、ロールコーター、リバースロールコーター、バーコーター、カーテンコーター、ダイスロットコーター、グラビアコーター、チャンプレックスコーター、2ロールサイズプレスコーター、ゲートロールサイズプレスコーター、フィルムメタリングサイズプレスコーター等の塗工装置を使用して、オンマシン方式またはオフマシン方式で原紙の表面に、単層または多層で塗工される。塗工時の顔料組成物の固形分濃度は、10〜75質量%の範囲で選ぶことができるが、塗工量が0.5〜10g/m2の範囲に留まるよう、また、塗工するコーターを考慮し、適宜調整することが好ましい。 When applying the coating material of the present invention to a base paper, a coating device generally used for coated paper production can be used, for example, blade coater, air knife coater, roll coater, reverse roll coater, bar coater, curtain coater. , Die-slot coater, gravure coater, champlex coater, 2-roll size press coater, gate roll size press coater, film metering size press coater, etc. The surface is coated in a single layer or multiple layers. The solid content concentration of the pigment composition at the time of coating can be selected in the range of 10 to 75% by mass, but is applied so that the coating amount remains in the range of 0.5 to 10 g / m 2. It is preferable to adjust appropriately considering the coater.
塗工包装用紙の場合、袋の外面にあたる面のみ印刷されることから、本発明も片面のみ塗工するほうが経済的に好ましい。ところが、片面のみ塗工すると紙は塗工面側にカールする性質があるので、カール矯正をするのが好ましい。カール矯正には、従来から行われている方法を選択することが可能である。なお、塗料を塗工するコーターとしてゲートロールコータを選択すると、表面を焼成カオリン含有の塗料を塗工し、裏面をカール矯正用の塗料を1回のパスで同時に塗工できるので、ゲートロールで塗工することが経済的により好ましい。 In the case of coated wrapping paper, only the surface corresponding to the outer surface of the bag is printed, and therefore it is economically preferable for the present invention to coat only one side. However, when only one side is coated, the paper has a property of curling to the coated surface side, so it is preferable to correct the curl. For curl correction, a conventional method can be selected. If a gate roll coater is selected as the coater to apply the paint, the surface can be coated with a baked kaolin-containing paint and the back side can be applied simultaneously with a curl correction paint in one pass. It is more economically preferable to apply.
本発明で塗工された塗工包装用紙は、塗工面や印刷適性をさらに向上させるために、カレンダー処理をすることが出来る。例えば、金属ロール間でニップするマシンカレンダーや弾性ロールにコットンロールを用いたスーパーカレンダーや弾性ロールに合成樹脂ロールを用いたソフトニップが挙げられる。ソフトニップカレンダーは合成樹脂ロール表面の耐熱温度がコットンロールに比べて高く設定することが可能なため、高温での処理が可能であり、同一の平滑性を目標とした場合、スーパーカレンダーに比べて処理線圧を低く設定できるので好ましい態様である。 The coated packaging paper coated according to the present invention can be subjected to a calendar process in order to further improve the coated surface and printability. For example, a machine calender that nips between metal rolls, a super calender that uses a cotton roll as an elastic roll, and a soft nip that uses a synthetic resin roll as an elastic roll. The soft nip calender can set the heat-resistant temperature on the surface of the synthetic resin roll higher than that of the cotton roll, so it can be processed at high temperatures, and compared with the super calender when the same smoothness is targeted. This is a preferred embodiment because the treatment linear pressure can be set low.
クラフトパルプは高強度を確保することが出来るため、本発明の塗工包装用紙原紙に晒、未晒、半晒クラフトパルプを少なくとも1種を含有する。クラフトパルプの種類は特に限定がなく、例えば、針葉樹未晒クラフトパルプ(以下、NUKPという)、広葉樹未晒クラフトパルプ(以下、LUKPという)、針葉樹晒クラフトパルプ(以下、NBKPという)、広葉樹晒クラフトパルプ(以下、LBKP)、針葉樹や広葉樹を用いて晒工程を酸素晒工程まで行った針葉樹酸素晒クラフトパルプ(NOKP)、広葉樹酸素晒クラフトパルプ(LOKP)、または、晒を1段から2段行った半晒パルプ等があげられ、これらの中から1種以上を適宜選択して用いる。 Since kraft pulp can ensure high strength, it contains at least one kind of bleached, unbleached, and semi-bleached kraft pulp on the coated and wrapping paper base paper of the present invention. The type of kraft pulp is not particularly limited. For example, softwood unbleached kraft pulp (hereinafter referred to as NUKP), hardwood unbleached kraft pulp (hereinafter referred to as LUKP), softwood bleached kraft pulp (hereinafter referred to as NBKP), hardwood bleached kraft. Pulp (hereinafter referred to as LBKP), conifer oxygen bleached kraft pulp (NOKP), hardwood oxygen bleached kraft pulp (LOKP), or bleaching performed from the first stage to the second stage. Semi-bleached pulp, etc., and one or more of these are appropriately selected and used.
上記クラフトパルプ以外に紙の強度を阻害しない範囲において、例えば、雑誌古紙、チラシ古紙、新聞古紙、オフィス古紙、情報用紙古紙、段ボール古紙、紙器古紙等の古紙パルプを必要に応じて脱墨処理をして使用することが可能である。 In addition to the above-mentioned kraft pulp, as long as it does not impair the strength of the paper, for example, waste paper pulp such as waste magazine paper, flyer waste paper, newspaper waste paper, office waste paper, information paper waste paper, cardboard waste paper, paper container waste paper, etc. Can be used.
内添薬品は必要に応じて使用でき、例えば、硫酸バンド、ロジン等のサイズ剤、ポリアミド、澱粉等の紙力増強剤、濾水歩留まり向上剤、ポリアミドポリアミンエピクロヒドリン等の耐水化剤、染料等が使用される。例示したパルプ、内添薬品を使用した原紙を使用する。 The internal chemicals can be used as necessary, for example, sizing agents such as sulfate bands and rosins, paper strength enhancers such as polyamide and starch, drainage yield improvers, water resistance agents such as polyamide polyamine epichlorohydrin, Dyes are used. The illustrated pulp and base paper using internal chemicals are used.
原紙の抄紙条件においても特に限定は無く、例えば、長網式抄紙機、ギャップフォーマー型抄紙機、丸網式抄紙機、短網式抄紙機等の商業規模の抄紙機が、目的に応じて適宜選択して使用できる。抄紙方式としては、酸性抄紙、中性抄紙、弱アルカリ抄紙等のいずれの方式でも使用できる。これらの抄紙条件で抄紙された原紙の米坪としては、30〜180g/m2が製袋加工するのに適した坪量であり包装用紙として好ましい。より好ましくは、50〜150g/m2である。 There are no particular restrictions on the paper making conditions of the base paper, and for example, commercial scale paper machines such as long net paper machines, gap former paper machines, round net paper machines, short net paper machines, etc. It can be appropriately selected and used. As the papermaking method, any method such as acidic papermaking, neutral papermaking, and weak alkali papermaking can be used. The basis weight of the base paper made under these papermaking conditions is 30 to 180 g / m 2, which is a basis weight suitable for bag making, and is preferable as packaging paper. More preferably 50 to 150 g / m 2.
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、本発明はそれらの範囲に限定されるものでない。なお、例中の「部」、「%」は特に断わらない限り、質量部、質量%を示す。 Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to these ranges. In the examples, “parts” and “%” indicate parts by mass and mass% unless otherwise specified.
実施例1
(塗料の作成)
焼成カオリン(商品名:アンシレックス93、BASF社製)90部、カオリン(商品名:ミラグロスJ、BASF社製)10部、接着剤(商品名:PA−8064、エイアンドエル社製)15部、酸化澱粉(商品名:GRS−T110、王子コーンスターチ社製)20部(いずれも固形分換算)からなる塗料を、濃度40%となるよう調製した。
Example 1
(Creation of paint)
Baked kaolin (trade name: Ansilex 93, manufactured by BASF) 90 parts, Kaolin (trade name: Milagros J, manufactured by BASF) 10 parts, adhesive (trade name: PA-8064, manufactured by A & L), oxidation A paint composed of 20 parts of starch (trade name: GRS-T110, manufactured by Oji Cornstarch Co., Ltd.) (both in terms of solid content) was prepared to a concentration of 40%.
560mlCSFのNBKPを60%、460mlCSFのLBKPを40%のパルプスラリー中に、パルプ100%に対して、カチオン化澱粉(商品名:ピラーP3YK、ピラースターチ社製)0.35%、硫酸バンド1.3%、サイズ剤(商品名:ペローザーE3655、東邦化学工業社製)0.4%を添加して調製した紙料で抄紙し、引き続きゲートロール塗工装置により上記塗料を片面に乾燥重量が3g/m2(固形分)となるように塗工し、反対面には、酸化澱粉(商品名:GRS−T110、王子コーンスターチ社製)を0.5g/m2となるように塗工、乾燥後、カレンダー処理をして紙水分6.0%、坪量80g/m2の塗工包装用紙を得た。 In a pulp slurry of 60% NBKP of 560 ml CSF and 40% LBKP of 460 ml CSF, 0.35% of cationized starch (trade name: Pillar P3YK, manufactured by Pillar Starch Co., Ltd.), sulfuric acid band 1. Paper is made with a stock prepared by adding 3% and sizing agent (trade name: Perroser E3655, manufactured by Toho Chemical Co., Ltd.) 0.4%, and the dry weight is 3 g on one side using a gate roll coating device. / M 2 (solid content) is applied, and on the opposite side, oxidized starch (trade name: GRS-T110, manufactured by Oji Cornstarch Co., Ltd.) is applied and dried to 0.5 g / m 2. Thereafter, a calendar process was performed to obtain a coated packaging paper having a paper moisture content of 6.0% and a basis weight of 80 g / m 2 .
実施例2
実施例1において、塗料中の顔料を焼成カオリン70部、タルク(商品名:ミクロタッチ、日本ミストロン社製)30部とした以外は実施例1と同様にして塗工包装用紙を得た。
Example 2
A coated packaging paper was obtained in the same manner as in Example 1 except that 70 parts of calcined kaolin and 30 parts of talc (trade name: Microtouch, manufactured by Nippon Mystron) were used as the pigment in the paint.
実施例3
実施例1において、原紙中のパルプをNOKP35%、LOKP65%、塗料中の顔料を焼成カオリン30部、タルク70部、接着剤を5部、酸化澱粉を35部とした以外は、実施例1と同様にして塗工包装用紙を得た。
Example 3
In Example 1, except that the pulp in the base paper is NOKP 35%, LOKP 65%, the pigment in the paint is 30 parts calcined kaolin, 70 parts talc, 5 parts adhesive, and 35 parts oxidized starch. The coated wrapping paper was obtained in the same manner.
実施例4
実施例1において、原紙中のパルプをNUKP35%、LUKP50%、脱墨処理した新聞古紙パルプ15%、塗料中の顔料を焼成カオリン100部、酸化澱粉を10部、塗工量を1.5g/m2、反対面の澱粉塗布量を0.3g/m2とした以外は、実施例1と同様にして塗工包装用紙を得た。
Example 4
In Example 1, the pulp in the base paper is NUKP 35%, LUKP 50%, deinked waste newspaper pulp 15%, the pigment in the paint is 100 parts of calcined kaolin, 10 parts of oxidized starch, and the coating amount is 1.5 g / m 2, except that the starch coating weight on the opposite surface was 0.3 g / m 2, to obtain a coated packaging material in the same manner as in example 1.
実施例5
実施例1において、塗料中の顔料を焼成カオリン75部、タルク5部、カオリン10部、重質炭酸カルシウム(商品名:ハイドロカーブ90、備北粉化工業社製)10部、酸化澱粉を35部、接着剤を9部とした以外は、実施例1と同様にして塗工包装用紙を得た。
Example 5
In Example 1, the pigment in the paint was calcined 75 parts of kaolin, 5 parts of talc, 10 parts of kaolin, 10 parts of heavy calcium carbonate (trade name: Hydrocurve 90, manufactured by Bihoku Flour & Chemical Co., Ltd.), and 35 parts of oxidized starch. A coated wrapping paper was obtained in the same manner as in Example 1 except that the adhesive was 9 parts.
比較例1
実施例1の原紙上に、酸化澱粉を両面での塗工量0.4g/m2になるように塗工、乾燥後、カレンダー処理をして紙水分6.0%の包装用紙を得た。
Comparative Example 1
The oxidized starch was coated on the base paper of Example 1 so that the coating amount on both sides was 0.4 g / m 2 , dried, and then calendered to obtain a packaging paper having a paper moisture of 6.0%. .
比較例2
実施例1において、塗料中の顔料を焼成カオリン8部、カオリン46部、重質炭酸カルシウム46部、接着剤を11部、酸化澱粉を5部、塗工量を7.5g/m2とした以外は、実施例1と同様にして塗工包装用紙を得た。
Comparative Example 2
In Example 1, the pigment in the paint was calcined kaolin 8 parts, kaolin 46 parts, heavy calcium carbonate 46 parts, adhesive 11 parts, oxidized starch 5 parts, and coating amount 7.5 g / m 2 . Except for the above, coated paper was obtained in the same manner as in Example 1.
比較例3
実施例2において、原紙中のパルプを脱墨処理した新聞古紙パルプ50%、脱墨処理した雑誌古紙パルプ50%、塗料中の酸化澱粉を50部とした以外は、実施例2と同様にして塗工包装用紙を得た。
Comparative Example 3
In Example 2, the same procedure as in Example 2 except that 50% of the newspaper waste paper pulp was deinked from the pulp in the base paper, 50% of the magazine waste paper pulp was deinked, and 50 parts of oxidized starch in the paint. Coated packaging paper was obtained.
比較例4
実施例1において、塗料中の顔料をカオリン30部、重質炭酸カルシウム70部、接着剤を9部、酸化澱粉を5部とした以外は、実施例1と同様にして塗工包装用紙を得た。
Comparative Example 4
In Example 1, coated wrapping paper was obtained in the same manner as in Example 1 except that the pigment in the paint was 30 parts kaolin, 70 parts heavy calcium carbonate, 9 parts adhesive, and 5 parts oxidized starch. It was.
比較例5
ヤンキードライヤーを備えた抄紙機で抄紙した包装用紙を用いた。
Comparative Example 5
Wrapping paper made with a paper machine equipped with a Yankee dryer was used.
比較例6
実施例1において、塗料中の顔料を焼成カオリン20部、カオリン30部、重質炭酸カルシウム50部、接着剤を6部、酸化澱粉を20部、反対面をポリビニアルアルコール(PVA−105、クラレ社製)0.5g/m2とした以外は、実施例1と同様にして塗工包装用紙を得た。
Comparative Example 6
In Example 1, 20 parts of calcined kaolin, 30 parts of kaolin, 50 parts of heavy calcium carbonate, 6 parts of adhesive, 20 parts of oxidized starch, and polyvinyl alcohol (PVA-105, Coated packaging paper was obtained in the same manner as in Example 1 except that the amount was 0.5 g / m 2 ( Kuraray Co., Ltd.)
得られた塗工包装用紙について、下記の評価方法で評価を行い、得られた結果を表1に示した。なお、本発明における塗工包装用紙の測定及び評価については特に記載のない限り、23℃、50%RHの環境下で行った。 The obtained coated wrapping paper was evaluated by the following evaluation method, and the obtained results are shown in Table 1. The measurement and evaluation of the coated wrapping paper in the present invention were performed in an environment of 23 ° C. and 50% RH unless otherwise specified.
(水に対する吸収係数Kaの測定)
JAPAN TAPPI No.51に準拠して液体動的吸収性試験機(熊谷理機工業社製)で測定した。
(Measurement of absorption coefficient Ka for water)
JAPAN TAPPI No. 51, a liquid dynamic absorbency tester (manufactured by Kumagai Riki Kogyo Co., Ltd.) was used.
(動的接触角)
動的接触角測定装置(商品名:DAT1100MK II、Fibro社製)を用い、蒸留水を4.0μm滴下後0.1秒後から5秒後までの接触角を測定して、0.1〜1.0秒間の低下した接触角度を0.9で除し、1秒間当たりに低下する接触角度を算出した。
(Dynamic contact angle)
Using a dynamic contact angle measuring device (trade name: DAT1100MK II, manufactured by Fibro), the contact angle from 0.1 second to 5 seconds after dropping 4.0 μm of distilled water was measured. The contact angle that decreased for 1.0 second was divided by 0.9, and the contact angle that decreased per second was calculated.
(フレキソ印刷におけるインキの発色性)
K印刷プルーファー(RK Print−Coat Instruments社製)、100線/インチに彫刻したアニロックスプレートで、水性フレキソ藍インキ(商品名:ラップトーンHR、サカタインクス社製)を使用して、得られた塗工包装用紙に印刷した。印刷した面をカラー反射濃度計(Model404G、X−Rite社製)でシアンインキ濃度を計測した。
(Color development of ink in flexographic printing)
K printing proofer (manufactured by RK Print-Coat Instruments), an anilox plate engraved at 100 lines / inch, using water-based flexo indigo ink (trade name: Laptone HR, manufactured by Sakata Inks) Printed on craft paper. The printed surface was measured for cyan ink density with a color reflection densitometer (Model 404G, manufactured by X-Rite).
(印刷部インキ流れ)
上記K印刷プルーファーにて印刷した部分を観察し、印刷面のインキが均一に定着されているかを拡大鏡と目視で評価した。
[評価基準]
◎:拡大鏡、目視ともインキが均一に定着されている。
○:拡大して印刷部分を観察すると、不均一部が一部存在するが、目視では均一に定着
されている。
×:インキが用紙に吸収し難く、余ったインキが泳いでおり、目視の観察でインキ定着
面が不均一である。
(Printing part ink flow)
The portion printed by the K printing proofer was observed, and whether or not the ink on the printing surface was uniformly fixed was visually evaluated with a magnifying glass.
[Evaluation criteria]
(Double-circle): The ink is uniformly fixed with a magnifier and visual observation.
○: When magnifying and observing the printed part, there are some non-uniform parts, but they are fixed uniformly by visual inspection.
X: The ink is difficult to absorb on the paper, the excess ink is swimming, and the ink fixing surface is uneven by visual observation.
(インキ乾燥性)
上記K印刷プルーファーで印刷した5秒後に合成紙(商品名:ユポ、ユポコーポレーション社製)を接触、圧着させて未乾燥インキの合成紙への転移を目視評価した。
[評価基準]
◎:全くインキが転移しない。
○:ごく一部のインキが転移したが、実用範囲である。
×:インキが乾燥せず、多くのインキ転移が認められた。
(Ink drying)
Synthetic paper (trade name: YUPO, manufactured by YUPO Corporation) was contacted and pressure-bonded 5 seconds after printing with the K printing proofer, and the transfer of the undried ink to the synthetic paper was visually evaluated.
[Evaluation criteria]
A: Ink does not transfer at all.
○: A small part of the ink was transferred, but it was within the practical range.
X: The ink did not dry and many ink transfers were recognized.
(製袋適性)
自動製袋機で、底幅115mm、袋幅315mm、袋長さ315mmの角底袋(手提げ袋)に加工した。加工後に折部の割れ、印刷部の割れを総合的に目視評価した。
[評価基準]
◎:全く割れが発生しない。
○:ごく一部割れが発生したが、実用範囲である。
×:割れが定常的に発生した。
(Bag making suitability)
Using an automatic bag making machine, it was processed into a square bottom bag (hand bag) having a bottom width of 115 mm, a bag width of 315 mm, and a bag length of 315 mm. After processing, cracks in the folded part and cracks in the printed part were comprehensively evaluated visually.
[Evaluation criteria]
(Double-circle): A crack does not generate | occur | produce at all.
○: Although a partial crack occurred, it was within the practical range.
X: The crack generate | occur | produced regularly.
上記表1に明らかなように、本発明の要件を満たす実施例1〜5は本発明の要件をいずれか欠く比較例1〜6に対して、印刷部のインキ流れがなく、インキ発色性やインキ乾燥性に優れ、製袋適性が良好であった。
以上の通り、本発明によりフレキソ印刷インキ、特に水性フレキソインキに対して、優れたインキ発色性と印刷面の仕上がりを持ち、さらに製袋適性に優れた塗工包装用紙を得ることが可能となった。
As is apparent from Table 1 above, Examples 1 to 5 satisfying the requirements of the present invention have no ink flow in the printing part, and ink coloring property and Comparative Examples 1 to 6 lacking any of the requirements of the present invention. Excellent ink drying properties and good bag making suitability.
As described above, according to the present invention, it is possible to obtain a coated and wrapping paper having excellent ink coloring properties and a printed surface finish for flexographic inks, particularly water-based flexographic inks, and having excellent bag forming suitability. It was.
Claims (3)
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014070316A (en) * | 2012-09-28 | 2014-04-21 | Daio Paper Corp | Liner and corrugated board sheet |
CN108978333A (en) * | 2018-08-15 | 2018-12-11 | 马鞍山卓凡新材料科技有限公司 | A kind of degradable antibacterial packaging bag convenient to use |
CN108978332A (en) * | 2018-08-15 | 2018-12-11 | 马鞍山卓凡新材料科技有限公司 | A kind of preparation method of environment-protective food package bag |
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JPH09170195A (en) * | 1995-10-13 | 1997-06-30 | Nippon Paper Ind Co Ltd | Production of coated paper for offset printing and coated paper |
JP2001248097A (en) * | 1999-12-27 | 2001-09-14 | Oji Paper Co Ltd | Paper for packaging |
JP2004094725A (en) * | 2002-09-02 | 2004-03-25 | Matsushita Electric Ind Co Ltd | Firmware rewriting device and firmware rewriting method |
JP2004232123A (en) * | 2003-01-29 | 2004-08-19 | Kishu Paper Co Ltd | Lightproof paper |
JP2008266865A (en) * | 2007-03-23 | 2008-11-06 | Oji Paper Co Ltd | Coating liner and corrugated board using the same |
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JPH09170195A (en) * | 1995-10-13 | 1997-06-30 | Nippon Paper Ind Co Ltd | Production of coated paper for offset printing and coated paper |
JP2001248097A (en) * | 1999-12-27 | 2001-09-14 | Oji Paper Co Ltd | Paper for packaging |
JP2004094725A (en) * | 2002-09-02 | 2004-03-25 | Matsushita Electric Ind Co Ltd | Firmware rewriting device and firmware rewriting method |
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JP2008266865A (en) * | 2007-03-23 | 2008-11-06 | Oji Paper Co Ltd | Coating liner and corrugated board using the same |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2014070316A (en) * | 2012-09-28 | 2014-04-21 | Daio Paper Corp | Liner and corrugated board sheet |
CN108978333A (en) * | 2018-08-15 | 2018-12-11 | 马鞍山卓凡新材料科技有限公司 | A kind of degradable antibacterial packaging bag convenient to use |
CN108978332A (en) * | 2018-08-15 | 2018-12-11 | 马鞍山卓凡新材料科技有限公司 | A kind of preparation method of environment-protective food package bag |
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