JPH04327295A - Production of coated paper for printing - Google Patents
Production of coated paper for printingInfo
- Publication number
- JPH04327295A JPH04327295A JP9844391A JP9844391A JPH04327295A JP H04327295 A JPH04327295 A JP H04327295A JP 9844391 A JP9844391 A JP 9844391A JP 9844391 A JP9844391 A JP 9844391A JP H04327295 A JPH04327295 A JP H04327295A
- Authority
- JP
- Japan
- Prior art keywords
- paper
- coated paper
- printing
- crosslinking agent
- base paper
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000007639 printing Methods 0.000 title claims abstract description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 24
- 239000000049 pigment Substances 0.000 claims abstract description 20
- 239000011248 coating agent Substances 0.000 claims abstract description 16
- 238000000576 coating method Methods 0.000 claims abstract description 16
- 238000009736 wetting Methods 0.000 claims abstract description 16
- 238000003490 calendering Methods 0.000 claims abstract description 13
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 10
- 238000005507 spraying Methods 0.000 claims abstract description 10
- 239000000853 adhesive Substances 0.000 claims description 14
- 230000001070 adhesive effect Effects 0.000 claims description 14
- 239000008199 coating composition Substances 0.000 claims description 9
- 238000001035 drying Methods 0.000 claims description 7
- 125000003172 aldehyde group Chemical group 0.000 claims description 2
- 125000003700 epoxy group Chemical group 0.000 claims description 2
- 150000003755 zirconium compounds Chemical group 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 3
- 238000010186 staining Methods 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 18
- 239000011247 coating layer Substances 0.000 description 14
- 230000000694 effects Effects 0.000 description 11
- 239000007788 liquid Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000005516 engineering process Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 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
- 229920000126 latex Polymers 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000005995 Aluminium silicate Substances 0.000 description 4
- 235000012211 aluminium silicate Nutrition 0.000 description 4
- 239000004816 latex Substances 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 229920001131 Pulp (paper) Polymers 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
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- -1 etc. Chemical class 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical group O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 239000001254 oxidized starch Substances 0.000 description 2
- 235000013808 oxidized starch Nutrition 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 238000013441 quality evaluation Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- DUFCMRCMPHIFTR-UHFFFAOYSA-N 5-(dimethylsulfamoyl)-2-methylfuran-3-carboxylic acid Chemical compound CN(C)S(=O)(=O)C1=CC(C(O)=O)=C(C)O1 DUFCMRCMPHIFTR-UHFFFAOYSA-N 0.000 description 1
- 102100031260 Acyl-coenzyme A thioesterase THEM4 Human genes 0.000 description 1
- WRAGBEWQGHCDDU-UHFFFAOYSA-M C([O-])([O-])=O.[NH4+].[Zr+] Chemical compound C([O-])([O-])=O.[NH4+].[Zr+] WRAGBEWQGHCDDU-UHFFFAOYSA-M 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 102000011632 Caseins Human genes 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 101000638510 Homo sapiens Acyl-coenzyme A thioesterase THEM4 Proteins 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 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
- 238000010009 beating 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
- 229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011436 cob Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 238000004093 laser heating Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000013054 paper strength agent Substances 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- ZXAUZSQITFJWPS-UHFFFAOYSA-J zirconium(4+);disulfate Chemical compound [Zr+4].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZXAUZSQITFJWPS-UHFFFAOYSA-J 0.000 description 1
Landscapes
- Paper (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、印刷用塗被紙の製造方
法に関し、特にカレンダー処理技術と原紙および塗被組
成物を検討することにより、嵩高で高品質の印刷用塗被
紙を操業性良く製造する方法に関する。[Industrial Application Field] The present invention relates to a method for producing coated paper for printing, and in particular, by studying calendering technology, base paper, and coating composition, it is possible to produce coated paper for printing with high bulk and high quality. It relates to a method of manufacturing with good performance.
【0002】0002
【従来の技術】印刷用塗被紙は、印刷物のビジュアル化
、高級化が進む今日、ユーザーの要求に合った印刷用紙
として著しく増加している。そして特にインキ受理性・
印刷平滑・印刷光沢などの品質がより一層優れている印
刷用塗被紙が望まれている。これらの印刷用塗工紙の優
れた品質を得るために、多くの技術要因がある中でカレ
ンダー処理技術も重要な技術として無視できない。2. Description of the Related Art Coated paper for printing is increasing significantly as a printing paper that meets the needs of users in today's world where printed matter is becoming increasingly visual and sophisticated. And especially ink receptivity
There is a demand for coated paper for printing that has even better qualities such as printing smoothness and printing gloss. In order to obtain the excellent quality of these coated papers for printing, there are many technical factors, and calendering technology cannot be ignored as an important technology.
【0003】カレンダー処理技術は、金属・繊維・樹脂
などの材質から成るロールを組み合せた加圧ニップに紙
を通紙して、紙表面を平滑化することにより、紙外観や
印刷効果を高品質にする技術であり、ロール表面の性状
により高光沢紙用グロスカレンダー・艶消紙用マットカ
レンダーなどがある。[0003] Calendering technology improves the paper appearance and printing effect by passing the paper through a pressure nip that combines rolls made of materials such as metal, fiber, and resin to smooth the paper surface. Depending on the properties of the roll surface, there are gloss calendars for high-gloss paper and matte calendars for matte paper.
【0004】そして、一般に高平滑・高光沢の表面を得
るためには、ニップの圧力を高くしなければならず、そ
の結果紙の厚みが損なわれ、紙腰が無くなる欠点がある
。この問題を解決する方法として、加熱した高温ロール
によってカレンダー処理する方法や蒸気を噴霧してカレ
ンダー処理する方法が知られているが、それぞれ効果と
同時に欠点もある。[0004] In general, in order to obtain a highly smooth and glossy surface, it is necessary to increase the nip pressure, which results in a loss of paper thickness and paper stiffness. As methods for solving this problem, methods of calendering using heated high-temperature rolls and methods of calendering by spraying steam are known, but each method has advantages as well as drawbacks.
【0005】前者の加熱高温ロールによる方法は、低速
度の通紙においては効果を発揮するが、高速度の場合は
ニップ中の時間が短くなるため、短時間で紙表面に熱を
転移して可塑化することが困難になる。また、後者の蒸
気を噴霧する方法は、従来より検討されており、最近で
は本発明で用いる飽和蒸気でなく、過熱した蒸気を用い
る方法が、特開平2─160993号報に提案されてい
る。[0005] The former method using heated high-temperature rolls is effective when paper is passed at low speeds, but at high speeds, the time during the nip is shortened, so heat is transferred to the paper surface in a short time. It becomes difficult to plasticize. The latter method of atomizing steam has been studied in the past, and recently, a method using superheated steam instead of the saturated steam used in the present invention has been proposed in Japanese Patent Application Laid-Open No. 160993/1993.
【0006】しかし、蒸気を噴霧して塗被紙を可塑化し
た状態でカレンダー処理を行うと、塗被紙表面の微小部
分がロールに取られて、ロールの表面が白く曇る現象、
所謂ロール汚れが発生する。この現象は実験室的な少量
の試験では問題が見つからないとしても、実際の連続操
業では問題がある。また、蒸気を加熱して用いるとロー
ル汚れが一層激しく発生し、操業性をさらに悪化させて
しまうことがある。そして、品質向上をはかるためにロ
ール温度を高くすることも、蒸気を噴霧してカレンダー
処理する場合には、ロール汚れが特に顕著になる傾向が
ある。[0006] However, when the coated paper is plasticized by spraying steam and then subjected to calender treatment, minute portions of the coated paper surface are picked up by the roll, resulting in the phenomenon that the roll surface turns white and cloudy.
So-called roll staining occurs. Even if this phenomenon is not found to be a problem in a small-scale laboratory test, it is a problem in actual continuous operation. In addition, when heated steam is used, roll fouling becomes more severe, which may further deteriorate operability. In addition, when the roll temperature is increased to improve quality, and when calendering is performed by spraying steam, roll stains tend to become particularly noticeable.
【0007】通常、印刷用塗被紙の製造においては、1
0万m程度の連続操業が行われるため、何千m毎にロー
ルの手入れをしなければならない様では、実際の操業は
不可能である。[0007] Normally, in the production of coated paper for printing, 1
Since continuous operation is carried out for approximately 0,000 m, actual operation would be impossible if the rolls had to be maintained every several thousand m.
【0008】このように、飽和蒸気を噴霧してカレンダ
ー処理する技術の最大のポイントは、その効果を充分に
発揮させ、なお且つ操業性の安定化をはかることである
が、これらについては十分な研究がなされておらず、実
際の製造技術としては生かされていないのが現状である
。[0008] As described above, the main point of the technology of calendering by spraying saturated steam is to fully demonstrate its effects and to stabilize the operability, but there are insufficient The current situation is that no research has been done on it, and it is not being utilized as an actual manufacturing technology.
【0009】[0009]
【発明が解決しようとする課題】本発明は、特定の表面
物性を持つ原紙と特定の架橋剤を添加した塗被組成物を
使用することにより、飽和蒸気を噴霧してカレンダー処
理を行う技術を改良して、嵩高で平滑性に優れ、光沢度
の高い印刷用塗被紙を操業性良く製造する方法を提供す
るものである。[Problems to be Solved by the Invention] The present invention provides a technology for performing calender treatment by spraying saturated steam by using a base paper with specific surface properties and a coating composition containing a specific crosslinking agent. An object of the present invention is to provide a method for producing coated printing paper that is bulky, has excellent smoothness, and has high gloss with good operability.
【0010】0010
【課題を解決するための手段】本発明は、原紙上に顔料
と接着剤を主成分とする塗被組成物を塗被乾燥し、飽和
蒸気を紙に噴霧してカレンダー処理を行う印刷用塗被紙
の製造方法において、原紙の動的濡れ値が−0.30〜
+0.20gの原紙を使用し、且つ塗被組成物中に架橋
剤を全顔料に対して0.05〜5.0重量%含有させる
ことを特徴とする印刷用塗被紙の製造方法である。[Means for Solving the Problems] The present invention provides a printing coating in which a coating composition containing a pigment and an adhesive as main components is coated on a base paper, dried, and then calendered by spraying saturated steam onto the paper. In the method for manufacturing a cover paper, the dynamic wettability value of the base paper is -0.30 to
+0.20g of base paper is used, and the coating composition contains 0.05 to 5.0% by weight of a crosslinking agent based on the total pigment. .
【0011】[0011]
【作用】本発明者等は、飽和蒸気を噴霧してカレンダー
処理する方法の操業性について検討を行った結果、蒸気
が噴霧された塗被層はその熱と水分により可塑化され、
カレンダーの加圧ニップで平滑化され易くなり、顔料の
配向も促進される効果があるが、それと同時に塗被層中
の接着剤が膨潤溶融し塗被層の強度を低下させ、塗被層
の一部が僅かづつではあるがカレンダーロールの表面に
付着し続け、ついに連続操業性が不可能になることをつ
きとめた。[Function] The present inventors investigated the operability of a method of calendering by spraying saturated steam, and found that the coating layer sprayed with steam is plasticized by the heat and moisture.
The pressurized nip of the calendar makes it easier to smooth and promotes the orientation of pigments, but at the same time, the adhesive in the coating layer swells and melts, reducing the strength of the coating layer and causing damage to the coating layer. It was found that a small portion of the product continued to adhere to the surface of the calender roll, making continuous operation impossible.
【0012】そこで可塑化状態にある塗被層接着剤の強
度と原紙の表面物性に注目して鋭意研究を重ね、塗被組
成物に架橋剤を添加して接着剤の分子間にネットワーク
を作ると、飽和蒸気によって可塑化された状態において
も、接着剤の強度低下を抑えることができるため、本発
明の目的を達成できることを見出した。そして、その効
果は使用する原紙の動的濡れ値が特定の値の時に限って
大きく効果を発揮することを発見し、遂にこの発明を完
成した。[0012] Therefore, we conducted extensive research focusing on the strength of the coating layer adhesive in a plasticized state and the surface properties of the base paper, and added a crosslinking agent to the coating composition to create a network between the adhesive molecules. It has been found that the object of the present invention can be achieved because a decrease in the strength of the adhesive can be suppressed even in a state where it is plasticized by saturated steam. Then, they discovered that the effect is significant only when the dynamic wettability value of the base paper used is a specific value, and finally completed this invention.
【0013】本発明において、原紙の「動的濡れ値」と
は2cm×5cmの紙試験片を長手方向に水深12mm
まで16mm/secの速さで、静止した純水に浸漬し
、浸漬開始から2秒後に試験片にかかる力を測定し、こ
の測定値に試験片の浸漬体積による浮力を加算した力を
意味する。[0013] In the present invention, the "dynamic wetting value" of base paper refers to a 2 cm x 5 cm paper test piece placed in water at a depth of 12 mm in the longitudinal direction.
The test piece is immersed in stationary pure water at a speed of 16 mm/sec, and the force applied to the test piece is measured 2 seconds after the start of immersion, and the buoyant force due to the immersion volume of the test piece is added to this measured value. .
【0014】一般に試験片と水とが接触した瞬間は、接
触角θが0<θ<90°であるから、試験片に上向きの
力が働き濡れ値はマイナスを示す。その後試験片の濡れ
が進むと接触角θが大きくなりθ=90°となった時に
上向きの力はゼロとなり、さらに濡れが進むとθ>90
°となり試験片には下向きの力が働き濡れ値はプラスに
転ずる。Generally, at the moment when the test piece comes into contact with water, the contact angle θ is 0<θ<90°, so an upward force acts on the test piece and the wetting value shows a negative value. After that, as the wetting of the test piece progresses, the contact angle θ increases, and when θ = 90°, the upward force becomes zero, and as the wetting progresses further, θ > 90°.
°, and a downward force acts on the test piece, causing the wetting value to turn positive.
【0015】本発明において動的濡れ値の測定には、レ
スカ社製の「Dynamic Wettability
Tester WETT−3000」を使用した。In the present invention, the dynamic wettability value is measured using "Dynamic Wettability" manufactured by Reska.
Tester WETT-3000" was used.
【0016】本発明では、水浸漬後2秒後の動的濡れ値
が−0.30〜+0.20g、より好ましくは−0.2
5〜+0.10gの範囲の原紙を使用する。因に、原紙
の動的濡れ値が+0.20gよりも大きい場合には、本
発明で特定する塗被液を用いても、乾燥工程で塗被層が
乾燥されるまでに塗被層内の水分が急激に原紙に浸透す
るため、塗被層内の接着剤や架橋剤も原紙方向に移動し
てしまい、結果として塗被層表面の接着剤や架橋剤の量
が減少し、十分なネットワークが形成されずロール汚れ
は極めて悪いものとなってしまう。[0016] In the present invention, the dynamic wettability value 2 seconds after immersion in water is -0.30 to +0.20 g, more preferably -0.2.
A base paper in the range of 5 to +0.10 g is used. Incidentally, if the dynamic wetting value of the base paper is greater than +0.20g, even if the coating liquid specified in the present invention is used, the amount of water in the coating layer will be reduced by the time the coating layer is dried in the drying process. As moisture rapidly penetrates into the base paper, the adhesive and cross-linking agent in the coating layer also move toward the base paper, resulting in a decrease in the amount of adhesive and cross-linking agent on the surface of the coating layer, resulting in a sufficient network. is not formed, resulting in extremely bad roll stains.
【0017】一方、原紙の動的濡れ値が−0.30g未
満であると、原紙と塗被層の接着性が大きく低下してし
まい、塗被層内で十分なネットワークを形成しても、原
紙と塗被層の界面で部分的な剥離が生じるため、本発明
の所望の効果を得ることができない。On the other hand, if the dynamic wetting value of the base paper is less than -0.30 g, the adhesion between the base paper and the coating layer will be greatly reduced, and even if a sufficient network is formed within the coating layer, Since partial peeling occurs at the interface between the base paper and the coating layer, the desired effects of the present invention cannot be obtained.
【0018】原紙の動的濡れ値の調節は、パルプ組成、
叩解条件、填料の種類と添加量、紙力剤、内添サイズ剤
、紙面PH、表面サイズ剤、表面処理剤、乾燥条件など
個々の抄紙条件を適宜選択して行うことができる。また
、本発明でいう原紙の動的濡れ値は、従来から原紙の性
質を示すパラメーターとして一般に用いられているコッ
ブ吸水度やステッキヒトサイズ度の値とは一次的な相関
が認められない。The dynamic wetting value of the base paper can be adjusted by adjusting the pulp composition,
Individual papermaking conditions such as beating conditions, type and amount of filler added, paper strength agent, internal sizing agent, paper surface pH, surface sizing agent, surface treatment agent, drying conditions, etc. can be selected as appropriate. Further, the dynamic wetting value of the base paper as used in the present invention has no linear correlation with the values of Cobb water absorption and Steckcht sizing, which have been conventionally used as parameters to indicate the properties of the base paper.
【0019】なお、原紙の米坪については特に限定する
ものではなく、一般に30〜400g/m2 程度の範
囲で目的に応じて適宜選択して使用される。The weight per unit area of the base paper is not particularly limited, and is generally selected from a range of about 30 to 400 g/m 2 as appropriate depending on the purpose.
【0020】次に、本発明において塗被組成物に含有さ
せる架橋剤の添加量は全顔料に対して0.05〜5.0
重量%とする必要がある。架橋剤の添加量が0.05重
量%未満では、接着剤分子の三次元構造化の効果が低く
、そのためロール汚れ防止の作用が不十分となり、連続
操業を続けるとロール汚れを引き起こし操業不可能とな
ってしまう。一方、架橋剤の添加率を5.0重量%を越
えて多量に使用すると、架橋剤増加の効果は極めて少な
いばかりでなく、塗被液の粘度が上昇し塗被時の操業性
を悪化させてしまうため好ましくない。Next, in the present invention, the amount of the crosslinking agent to be added to the coating composition is 0.05 to 5.0 with respect to the total pigment.
It needs to be in weight%. If the amount of crosslinking agent added is less than 0.05% by weight, the effect of creating a three-dimensional structure of the adhesive molecules will be low, and therefore the effect of preventing roll staining will be insufficient, and if continuous operation is continued, roll stains will occur, making it impossible to operate. It becomes. On the other hand, if the addition rate of the crosslinking agent exceeds 5.0% by weight and is used in large quantities, not only will the effect of increasing the crosslinking agent be extremely small, but the viscosity of the coating liquid will increase and the operability during coating will deteriorate. This is not desirable because it causes
【0021】従って、架橋剤の添加量は全顔料に対して
0.05〜5.0重量%、より好ましくは0.1〜3.
0重量%の範囲で適宜調節して添加するのが望ましい。Therefore, the amount of crosslinking agent added is 0.05 to 5.0% by weight, more preferably 0.1 to 3.0% by weight based on the total pigment.
It is desirable to adjust the amount as appropriate within the range of 0% by weight.
【0022】本発明の架橋剤は、一般に製紙業界でオフ
セット印刷用・ラベル用・屋外ポスター用などの用途に
、耐水性を付与するために使用する架橋剤と同様のもの
で良く、最新紙加工便覧(テックタイムス編)P.46
9にその概要が記載されている。また、架橋剤の分子量
、分子構造については特に限定するものではないが、反
応基としてアルデヒド基を2基以上有するもの、例えば
グリオキザールなど、あるいは、エポキシ基を2基以上
有するもの、例えばグリコール類のジグリシジルエーテ
ル、ポリオール類のポリグリシジルエーテル、ジカルボ
ン酸類のジグリシジルエステルなど、さらに、ジルコニ
ウム化合物、例えば酢酸ジルコニウム、炭酸ジルコニウ
ムアンモニウム、硫酸ジルコニウムなどを用いた時にそ
の効果が著しく、ロールよごれ防止作用を大きく向上さ
せることができた。The crosslinking agent of the present invention may be the same as the crosslinking agent generally used in the paper manufacturing industry to impart water resistance for applications such as offset printing, labels, and outdoor posters, and is suitable for the latest paper processing. Handbook (edited by Tech Times) P. 46
9 provides an overview. The molecular weight and molecular structure of the crosslinking agent are not particularly limited, but those having two or more aldehyde groups as reactive groups, such as glyoxal, or those having two or more epoxy groups, such as glycols, etc. Diglycidyl ethers, polyglycidyl ethers of polyols, diglycidyl esters of dicarboxylic acids, etc., as well as zirconium compounds such as zirconium acetate, ammonium zirconium carbonate, zirconium sulfate, etc., have a remarkable effect, greatly increasing the roll fouling prevention effect. I was able to improve it.
【0023】本発明の方法ではカレンダーロールの表面
温度を50〜250℃の範囲に調整するとカレンダー平
滑化の効果がさらに増大する。また、カレンダーが塗被
機乾燥装置の直後に組み込まれているオンマシンカレン
ダーの場合は、ロール汚れが起きると全体の操業性の低
下となるため、特に本発明の方法を必要とするものであ
る。In the method of the present invention, the calender smoothing effect is further enhanced by adjusting the surface temperature of the calender roll to a range of 50 to 250°C. Furthermore, in the case of an on-machine calender in which the calender is installed immediately after the coater drying device, the method of the present invention is particularly required because roll fouling will reduce overall operability. .
【0024】本発明の方法では、原紙のパルプ組成とし
ては上質系あるいは中質系の印刷用塗被紙に用いられる
晒、未晒、半晒などのNKP、LKPおよび新聞、雑誌
、情報用紙、印刷紙などを処理した古紙再生パルプ、あ
るいはSGP、TMP、RGP、CTMPなどの高歩留
パルプなどが用いられ、その配合率は特に規定するもの
ではなく、適宜調節して使用される。In the method of the present invention, the pulp composition of the base paper includes bleached, unbleached, semi-bleached NKP, LKP, etc. used for high-quality or medium-quality coated printing paper, and newspapers, magazines, information paper, etc. Recycled waste paper pulp obtained by processing printing paper or the like, or high-yield pulp such as SGP, TMP, RGP, CTMP, etc., is used, and the blending ratio is not particularly specified and may be adjusted as appropriate.
【0025】また、原紙の抄紙方法については特に限定
されず、例えばトップワイヤー、ツインワイヤーを含む
長網マシン、一層または多層の丸網マシン、二者を併用
したマシン、ヤンキードライヤーマシンなどで酸性抄紙
、中性抄紙、アルカリ抄紙いずれであっても良く、また
、各種のサイズプレス、ビルブレードコーターなどで表
面処理や予備塗工を行うことも良い。[0025] The method of making the base paper is not particularly limited; for example, acid paper making is performed using a fourdrinier machine including a top wire or twin wire, a single layer or multilayer round net machine, a machine using a combination of the two, a Yankee dryer machine, etc. , neutral paper, or alkaline paper may be used, and surface treatment or preliminary coating may be performed using various size presses, bill blade coaters, or the like.
【0026】そして、本発明の方法で用いられる塗被組
成物の顔料としては、例えばクレー、カオリン、焼成カ
オリン、デラミネーテッドカオリン、構造性カオリン、
水酸化アルミニウム、重質炭酸カルシウム、軽質炭酸カ
ルシウム、二酸化チタン、硫酸バリウム、酸化亜鉛、サ
チンホワイト、タルク、プラスチックピグメント、バイ
ンダーピグメントなどのような通常の塗被紙用顔料の一
種または二種以上が適宜選択して使用される。Pigments in the coating composition used in the method of the present invention include, for example, clay, kaolin, calcined kaolin, delaminated kaolin, structured kaolin,
One or more of the usual coated paper pigments such as aluminum hydroxide, heavy calcium carbonate, light calcium carbonate, titanium dioxide, barium sulfate, zinc oxide, satin white, talc, plastic pigments, binder pigments, etc. It is selected and used as appropriate.
【0027】さらに、接着剤としては、例えばカゼイン
、大豆蛋白、合成蛋白などの蛋白類、スチレン・ブタジ
エン共重合体など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などのアクリル系重合体ラテ
ックス、エチレン・酢酸ビニル重合体などのビニル系重
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などの官能基含有単量体で変性した
アルカリ溶解性、アルカリ膨潤性あるいはアルカリ非溶
解性の重合体ラテックスおよびバインダーピグメントと
呼ばれる各種の合成樹脂重合体、ポリビニルアルコール
、オレフィン−無水マレイン酸樹脂、メラミン樹脂など
の合成樹脂系接着剤、酸化澱粉、陽性澱粉、エステル化
澱粉、デキストリンなどの澱粉類、カルボキシルメチル
セルロース、ヒドロキシエチルセルロースなどのセルロ
ース誘導体などのような通常の塗被紙用接着剤の一種ま
たは二種以上が適宜選択して使用される。Furthermore, examples of adhesives include proteins such as casein, soybean protein, and synthetic proteins; conjugated diene copolymer latex such as styrene-butadiene copolymer;
Acrylic polymer latices such as polymers or copolymers of acrylic esters and/or methacrylic esters, vinyl polymer latexes such as ethylene/vinyl acetate polymers, or various polymer latexes such as those with carboxyl groups, etc. Alkali-soluble, alkali-swellable, or alkali-insoluble polymer latex modified with functional group-containing monomers, various synthetic resin polymers called binder pigments, polyvinyl alcohol, olefin-maleic anhydride resin, melamine resin, etc. One or more types of common adhesives for coated paper, such as synthetic resin adhesives, starches such as oxidized starch, positive starch, esterified starch, and dextrin, and cellulose derivatives such as carboxymethyl cellulose and hydroxyethyl cellulose. are selected and used as appropriate.
【0028】なお、接着剤は顔料100重量部に対して
4〜50重量部、より好ましくは10〜30重量部程度
の範囲で配合される。また塗液中には必要に応じて消泡
剤、着色剤、離型剤、流動変性剤などの各助剤が適宜配
合される。そして、本発明では先に述べたように、架橋
剤を全顔料に対して0.05〜5.0重量%、状況に応
じて添加することが重要である。The adhesive is blended in an amount of 4 to 50 parts by weight, more preferably 10 to 30 parts by weight, based on 100 parts by weight of the pigment. In addition, various auxiliary agents such as an antifoaming agent, a coloring agent, a mold release agent, and a flow modifier are suitably blended into the coating liquid as required. In the present invention, as described above, it is important to add the crosslinking agent in an amount of 0.05 to 5.0% by weight based on the total pigment depending on the situation.
【0029】本発明の方法で用いられる塗被機としては
、一般の塗被紙製造に用いられる、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、ビルブレードコータ
ー、カーテンコーター、ダイスロットャーター、グラビ
アコーター、チャンプレックスコーター、サイズプレス
コーターなどの両面または片面塗被装置を設けたオンマ
シンあるいはオフマシンコーターによって塗被液が原紙
上に一層または多層に塗被される。Coating machines used in the method of the present invention include those used in general coated paper production, such as blade coaters, air knife coaters, roll coaters, reverse roll coaters, bar coaters, bill blade coaters, and curtain coaters. The coating liquid is coated on the base paper in one layer or in multiple layers by an on-machine or off-machine coater equipped with a double-sided or single-sided coating device such as a die slot coater, a gravure coater, a Champlex coater, or a size press coater.
【0030】その際の塗被液の固形分濃度は一般に40
〜75重量%程度であるが、操業性を考慮すると45〜
70重量%の範囲が好ましい。[0030] The solid content concentration of the coating liquid at that time is generally 40
〜75% by weight, but considering operability, it is 45〜75% by weight.
A range of 70% by weight is preferred.
【0031】また、湿潤塗被層を乾燥する方法としては
、従来から知られている蒸気加熱、熱風加熱、ガスヒー
ター加熱、高周波加熱、電気ヒーター加熱、赤外線ヒー
ター加熱、レーザー加熱、電子線加熱などの各種乾燥方
式が適宜採用できる。[0031] Methods for drying the wet coating layer include conventionally known steam heating, hot air heating, gas heater heating, high frequency heating, electric heater heating, infrared heater heating, laser heating, electron beam heating, etc. Various drying methods can be adopted as appropriate.
【0032】本発明の方法においては、かくして得られ
た塗被紙を、飽和蒸気を噴霧してカレンダー処理を行う
ものであるが、その蒸気量およびカレンダー圧力、ニッ
プ数については特に限定されず、要求される品質に応じ
て適宜選択される。本発明におけるカレンダーとしては
、例えばスーパーカレンダー、グロスカレンダー、ソフ
トコンパクトカレンダーなどの各種カレンダーがオンマ
シンやオフマシンの形態で使用される。そして、ここで
言うオンマシンカレンダーは、抄紙機に限らず塗工機に
組み込まれたオンコーターマシンカレンダーも含まれる
。In the method of the present invention, the coated paper thus obtained is calendered by spraying saturated steam, but the amount of steam, calender pressure, and number of nips are not particularly limited. It is selected as appropriate depending on the required quality. As the calendar in the present invention, various types of calendars such as a super calendar, a gross calendar, and a soft compact calendar are used in on-machine or off-machine formats. The on-machine calendar referred to herein is not limited to a paper machine, but also includes an on-coater machine calendar built into a coating machine.
【0033】[0033]
【実施例】以下に実施例を挙げて本発明をより具体的に
説明するが、勿論その範囲に限定するものではない。な
お例中の部および%は、特に断らない限りそれぞれ重量
部および重量%を示す。[Examples] The present invention will be explained in more detail with reference to Examples below, but of course the scope is not limited thereto. Note that parts and % in the examples indicate parts by weight and % by weight, respectively, unless otherwise specified.
【0034】実施例1〜3
全顔料中カオリン(商品名;UW−90、EMC社製)
70部、微粒化重質炭酸カルシウム25部、サチンホワ
イト分散液(商品名;サチンホワイト、白石工業社製)
5部(固形分)、と全顔料に対してポリアクリル酸ソー
ダ0.2%(固形分)をコーレス分散機を用いて分散し
、固形分濃度66%のスラリーを調製した。このスラリ
ーに全顔料100部に対して酸化澱粉4部(固形分)、
スチレン−ブタジエン共重合体ラテックス12部(固形
分)、および架橋剤を表1に示す種類と添加率(対全顔
料%)に基づきそれぞれ加え、さらに水を加えて固形分
濃度56%の塗被液を調製した。Examples 1 to 3 Kaolin in all pigments (trade name: UW-90, manufactured by EMC)
70 parts, 25 parts of atomized heavy calcium carbonate, Sachin White dispersion (trade name: Sachin White, manufactured by Shiraishi Kogyo Co., Ltd.)
5 parts (solid content) and 0.2% (solid content) of sodium polyacrylate based on the total pigment were dispersed using a Coles disperser to prepare a slurry with a solid content concentration of 66%. In this slurry, 4 parts of oxidized starch (solid content) per 100 parts of total pigment,
12 parts (solid content) of styrene-butadiene copolymer latex and a crosslinking agent were added based on the type and addition rate (% of total pigment) shown in Table 1, and then water was added to form a coating with a solid content concentration of 56%. A liquid was prepared.
【0035】この塗被液を、原紙の動的濡れ値が−0.
20g(実施例1)、−0.05g(実施例2)、+0
.10g(実施例3)、に調節して抄紙された米坪80
g/m2 の原紙に、片面当り乾燥重量で15g/m2
になるようにブレードコーターで両面塗被を行い、12
0℃の熱風乾燥機で乾燥して、水分5.8%の両面塗被
紙を得た。This coating liquid was applied to the base paper when the dynamic wetting value was -0.
20g (Example 1), -0.05g (Example 2), +0
.. 10g (Example 3)
g/m2 base paper, 15 g/m2 dry weight per side
Coat both sides with a blade coater so that
It was dried in a hot air dryer at 0°C to obtain a double-sided coated paper with a moisture content of 5.8%.
【0036】このようにして得られた両面塗被紙を、金
属ロールと弾性ロールで構成されるカレンダーで、金属
ロールの表面温度を40℃として、飽和蒸気を噴霧して
通紙し平滑化処理した。この時の線圧は250Kg/c
mで、速度は400m/minであった。The thus obtained double-sided coated paper was passed through a calender consisting of a metal roll and an elastic roll, with the surface temperature of the metal roll set to 40°C, and saturated steam was sprayed to smooth the paper. did. The linear pressure at this time is 250Kg/c
m, and the speed was 400 m/min.
【0037】実施例1〜3の各条件、即ち原紙の動的濡
れ値・塗被液の架橋剤の種類と添加率・連続操業性およ
び塗被紙の品質評価結果を表1に示した。Table 1 shows the conditions of Examples 1 to 3, namely, the dynamic wetting value of the base paper, the type and addition rate of the crosslinking agent in the coating liquid, the continuous operability, and the quality evaluation results of the coated paper.
【0038】実施例4
カレンダーの金属ロール表面温度を110℃・線圧を1
50Kg/cmとし、表1に示す架橋剤とした以外は、
実施例1と同様の方法で行った。この時の各条件と結果
を表1に示した。Example 4 The surface temperature of the metal roll of the calender was 110°C and the linear pressure was 1
50Kg/cm, except that the crosslinking agent shown in Table 1 was used.
The same method as in Example 1 was used. Table 1 shows the conditions and results at this time.
【0039】実施例5
カレンダーが塗被機の乾燥機の直後に組み込まれている
1ニップカレンダーで、金属ロール表面温度を90℃・
線圧を200Kg/cmとし、表1に示す架橋剤の種類
と添加率とした以外は、実施例1と同様の方法で行い、
各条件と結果を表1に示した。Example 5 A 1-nip calender was installed in the coater immediately after the dryer, and the surface temperature of the metal roll was kept at 90°C.
It was carried out in the same manner as in Example 1, except that the linear pressure was 200 kg/cm and the type and addition rate of the crosslinking agent were as shown in Table 1.
Table 1 shows each condition and result.
【0040】比較例1
実施例2において、動的濡れ値が+0.30gの原紙を
用いた以外は同様にして両面塗被紙を得た。この時の連
続操業性、および塗被紙の品質評価結果を表1に示した
。Comparative Example 1 A double-sided coated paper was obtained in the same manner as in Example 2, except that a base paper with a dynamic wetting value of +0.30 g was used. Table 1 shows the continuous operation performance and the quality evaluation results of the coated paper.
【0041】比較例2
実施例2において、動的濡れ値が−0.35gの原紙を
用いた以外は同様にして両面塗被紙を得た。この時の結
果を表1に示した。Comparative Example 2 A double-sided coated paper was obtained in the same manner as in Example 2, except that a base paper with a dynamic wetting value of -0.35 g was used. The results are shown in Table 1.
【0042】比較例3〜4
表1に示す架橋剤の種類と添加率とした以外は実施例1
と同様にして行い、結果を表1に示した。Comparative Examples 3 to 4 Example 1 except that the type and addition rate of the crosslinking agent were as shown in Table 1.
The results are shown in Table 1.
【0043】〔測定方法、評価方法〕
光沢度 ;JIS−P8142に準じて測定した
。
数値が大きい程光沢が良い。
連続操業性;○・・・10時間以上の連続操業が可能。
×・・・塗被層よりラテックスや顔料接着剤などが剥離
してカレンダーロール表面に付着し10時間以上の連続
操業が不可能。[Measurement method and evaluation method] Glossiness: Measured according to JIS-P8142. The higher the number, the better the gloss. Continuous operation: ○: Continuous operation for 10 hours or more is possible. ×: Latex, pigment adhesive, etc. peeled off from the coating layer and adhered to the calender roll surface, making continuous operation for 10 hours or more impossible.
【0044】[0044]
【表1】[Table 1]
【0045】[0045]
【発明の効果】表1に示す実施例の結果から明らかなよ
うに、本発明の方法で得られた印刷用塗被紙は、連続操
業性に優れ、且つ塗被紙光沢度に優れたものであった。[Effects of the Invention] As is clear from the results of the examples shown in Table 1, the coated paper for printing obtained by the method of the present invention has excellent continuous operability and coated paper gloss. Met.
Claims (6)
組成物を塗被乾燥し、飽和蒸気を紙に噴霧してカレンダ
ー処理を行う印刷用塗被紙の製造方法において、原紙の
動的濡れ値が−0.30〜+0.20gの原紙を使用し
、且つ塗被組成物中に架橋剤を全顔料に対して0.05
〜5.0重量%含有させることを特徴とする印刷用塗被
紙の製造方法。[Claim 1] A method for producing coated paper for printing, which comprises coating a base paper with a coating composition containing a pigment and an adhesive as main components, drying the base paper, and then calendering the paper by spraying the paper with saturated steam. A base paper with a dynamic wetting value of -0.30 to +0.20 g is used, and the coating composition contains a crosslinking agent of 0.05 g based on the total pigment.
A method for producing coated paper for printing, characterized in that the content is 5.0% by weight.
0℃である請求項1記載の印刷用塗被紙の製造方法。[Claim 2] The surface temperature of the calender roll is 50 to 25.
The method for producing coated paper for printing according to claim 1, wherein the temperature is 0°C.
項1記載の印刷用塗被紙の製造方法。3. The method for producing coated paper for printing according to claim 1, wherein the reactive group of the crosslinking agent is an aldehyde group.
1記載の印刷用塗被紙の製造方法。4. The method for producing coated paper for printing according to claim 1, wherein the reactive group of the crosslinking agent is an epoxy group.
1記載の印刷用塗被紙の製造方法。5. The method for producing coated paper for printing according to claim 1, wherein the crosslinking agent is a zirconium compound.
込まれたカレンダーである請求項1記載の印刷用塗被紙
の製造方法。6. The method for producing coated paper for printing according to claim 1, wherein the calendar is a calendar installed immediately after the coater drying device.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9844391A JPH04327295A (en) | 1991-04-30 | 1991-04-30 | Production of coated paper for printing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9844391A JPH04327295A (en) | 1991-04-30 | 1991-04-30 | Production of coated paper for printing |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04327295A true JPH04327295A (en) | 1992-11-16 |
Family
ID=14219899
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9844391A Pending JPH04327295A (en) | 1991-04-30 | 1991-04-30 | Production of coated paper for printing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04327295A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5789031A (en) * | 1995-03-30 | 1998-08-04 | Oji Paper Co., Ltd. | Process for manufacturing coated paper |
JP2006193864A (en) * | 2005-01-14 | 2006-07-27 | Nippon Paper Industries Co Ltd | Method for producing coated paper for printing |
JP2006200109A (en) * | 2004-12-22 | 2006-08-03 | Nippon Paper Industries Co Ltd | Method for producing coated paper for printing and coated paper |
JP2007169874A (en) * | 1995-10-05 | 2007-07-05 | Metso Paper Inc | Apparatus for coating moving paper or cardboard web |
JP2010070872A (en) * | 2008-09-17 | 2010-04-02 | Oji Paper Co Ltd | Coated paper |
-
1991
- 1991-04-30 JP JP9844391A patent/JPH04327295A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5789031A (en) * | 1995-03-30 | 1998-08-04 | Oji Paper Co., Ltd. | Process for manufacturing coated paper |
JP2007169874A (en) * | 1995-10-05 | 2007-07-05 | Metso Paper Inc | Apparatus for coating moving paper or cardboard web |
JP2006200109A (en) * | 2004-12-22 | 2006-08-03 | Nippon Paper Industries Co Ltd | Method for producing coated paper for printing and coated paper |
JP2006193864A (en) * | 2005-01-14 | 2006-07-27 | Nippon Paper Industries Co Ltd | Method for producing coated paper for printing |
JP4645199B2 (en) * | 2005-01-14 | 2011-03-09 | 日本製紙株式会社 | Method for producing coated paper for printing |
JP2010070872A (en) * | 2008-09-17 | 2010-04-02 | Oji Paper Co Ltd | Coated paper |
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