JPH01139895A - Production of cast coat paper - Google Patents
Production of cast coat paperInfo
- Publication number
- JPH01139895A JPH01139895A JP29172787A JP29172787A JPH01139895A JP H01139895 A JPH01139895 A JP H01139895A JP 29172787 A JP29172787 A JP 29172787A JP 29172787 A JP29172787 A JP 29172787A JP H01139895 A JPH01139895 A JP H01139895A
- Authority
- JP
- Japan
- Prior art keywords
- latex
- paper
- cast
- temperature
- glass transition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000004816 latex Substances 0.000 claims abstract description 48
- 229920000126 latex Polymers 0.000 claims abstract description 48
- 239000011248 coating agent Substances 0.000 claims abstract description 27
- 238000000576 coating method Methods 0.000 claims abstract description 27
- 239000007788 liquid Substances 0.000 claims abstract description 23
- 239000000853 adhesive Substances 0.000 claims abstract description 12
- 230000001070 adhesive effect Effects 0.000 claims abstract description 12
- 230000009477 glass transition Effects 0.000 claims abstract description 10
- 239000000049 pigment Substances 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims description 30
- 239000012752 auxiliary agent Substances 0.000 claims description 7
- 238000001035 drying Methods 0.000 abstract description 15
- 238000003825 pressing Methods 0.000 abstract description 4
- 239000002075 main ingredient Substances 0.000 abstract 1
- 238000007761 roller coating Methods 0.000 abstract 1
- 239000011247 coating layer Substances 0.000 description 31
- 229920000642 polymer Polymers 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000005266 casting Methods 0.000 description 10
- 239000010410 layer Substances 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 6
- 230000008859 change Effects 0.000 description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical class [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- -1 amide compound Chemical class 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000005018 casein Substances 0.000 description 4
- 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 4
- 235000021240 caseins Nutrition 0.000 description 4
- 239000008199 coating composition Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229910052749 magnesium Chemical class 0.000 description 4
- 239000011777 magnesium Chemical class 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000015271 coagulation Effects 0.000 description 3
- 238000005345 coagulation Methods 0.000 description 3
- 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 3
- 235000018102 proteins Nutrition 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 108010073771 Soybean Proteins Proteins 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 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
- 230000008901 benefit Effects 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000701 coagulant Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 150000004675 formic acid derivatives Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 239000006082 mold release agent Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 2
- 235000019710 soybean protein Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 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
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Landscapes
- Paper (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はキャストコート紙の製造方法、特にリウェツト
法の改良に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for producing cast coated paper, particularly to improvements in the rewetting method.
キャストコート紙と呼ばれる印刷用強光沢塗被紙の製造
方法としては、湿潤状態の塗被層を加熱ドラム面に圧接
して光沢仕上げする直接法、湿潤状態の塗被層を凝固剤
溶液と接触させゲル化させてから、加熱ドラム面に圧接
して光沢仕上げする凝固法、湿潤状態の塗被層を一旦乾
燥又は半乾燥した後、再湿潤によシ可塑化して加熱ドラ
ム面に圧接するリウェツト・キャスト法等が知られてい
る。There are two methods of manufacturing highly glossy coated paper for printing called cast coated paper: the direct method, in which a wet coating layer is pressed against the surface of a heated drum for a glossy finish, and the wet coating layer is brought into contact with a coagulant solution. A coagulation method in which the wet coating layer is dried or semi-dried and then plasticized by rewetting and then pressed against the heated drum surface.・Cast method etc. are known.
これらのキャスト仕上げ方法に、いずれも可塑状態にあ
る塗被層を加熱ドラム面に圧接乾燥し、離型させる点で
共通しているが、塗被層の可塑状態の違いによって、操
業性及び得られるキャスト塗被紙の品質に差が生ずる。All of these cast finishing methods have in common that the coating layer in a plastic state is pressed against the surface of a heated drum and then released from the mold, but the differences in the plasticity of the coating layer affect operability and yield. There is a difference in the quality of cast coated paper.
即ち、直接法でに、加熱ドラムの表面温度を100℃以
上にすると、塗被液の沸騰が起り塗被層が破壊されてし
まうので、ドラム温度1100℃以下とせざるを得すキ
ャストスピードは低速となる。In other words, in the direct method, if the surface temperature of the heating drum is increased to over 100°C, the coating liquid will boil and the coating layer will be destroyed, so the drum temperature must be kept below 1100°C and the casting speed must be slow. becomes.
凝固法では、塗被層がゲル化されているため、加熱ドラ
ム面の温度を100℃以上に上げることも可能であるが
、塗被層中に含まれる水分が多くドラムからの剥離性が
悪いこと、また、塗被層の凝固の度合を調節するのも困
難ななめ実際ににあtb高速での仕上が出来ない。In the coagulation method, since the coating layer is gelatinized, it is possible to raise the temperature of the heating drum surface to over 100℃, but the coating layer contains a lot of water and has poor peelability from the drum. In addition, it is difficult to control the degree of coagulation of the coated layer, so finishing at high speed is not possible.
ま九、リウェツト法では、塗被層を一旦乾燥させる九め
、加熱ドラム面の温度t−90〜180℃まで上げるこ
とも可能であるが、−旦乾燥された塗被層を再湿潤する
念めに可塑化の度合が他の方法に比較して著しく低い。In the rewetting method, it is possible to dry the coating layer once and then raise the temperature of the heating drum surface to t-90 to 180℃, but it is necessary to rewet the coating layer once it has been dried. Therefore, the degree of plasticization is significantly lower than that of other methods.
再湿潤による可塑化を容易にするため再湿潤液にアミド
化合物を含有せしめる(q#開昭59−f 92797
号公報)等の工夫がなされているが、それでもな訃可塑
化の程度は低く、そのため塗被層が加熱ドラム面に均一
に密着されず、低速度下での操業に於てに比較的均質な
強光沢の塗被紙が得られるものの、高速度操業になるに
従って、光沢ムラやピンホール状の斑点等が発生し、塗
被面の均質性が急激に失われてしまう。In order to facilitate plasticization by rewetting, the rewetting liquid contains an amide compound (q# Kaisho 59-f 92797
However, the degree of plasticization is still low, and as a result, the coating layer does not adhere uniformly to the surface of the heating drum, resulting in a relatively homogeneous coating during operation at low speeds. Although coated paper with a strong gloss can be obtained, as the speed of operation increases, uneven gloss, pinhole-like spots, etc. occur, and the uniformity of the coated surface is rapidly lost.
又、塗被層の加熱ドラムへの密着を良くするため、再湿
潤する前の塗被層をスーパーカレンダー掛けして平滑化
しておく方法や、塗被層を仕上げ面に圧接する際のプレ
スロール圧を高圧にする方法も提案されているが、これ
らの方法に一方でキャスト塗被紙の特徴である低緊度で
嵩高という利点を著しく損なってしまう。In addition, in order to improve the adhesion of the coating layer to the heated drum, there is a method of smoothing the coating layer by applying a super calender before rewetting it, and a method of smoothing the coating layer before it is re-wetted, and a method of using a press roll when pressing the coating layer to the finished surface. Methods of increasing the pressure have also been proposed, but on the other hand, these methods significantly impair the advantages of cast coated paper, which are low tension and high bulk.
又、塗被層をポーラスにして加熱ドラムへの密着を良く
するように亜鉛、アルミニウム、マグネシュウムの塩類
を塗被液に添加する方法(特開昭60−146097号
公報)も提案されているが、この方法は、出来上つ九キ
ャスト塗被紙の表面強度が弱くなり接着剤を増す必要が
あり、このために、塗被層の可塑化はそれ程良くならな
い。Additionally, a method has been proposed in which salts of zinc, aluminum, and magnesium are added to the coating liquid to make the coating layer porous and improve adhesion to the heating drum (Japanese Patent Laid-Open No. 146097/1983). However, this method reduces the surface strength of the finished cast coated paper and requires an increase in adhesive, so that the plasticization of the coated layer is not as good.
本発明ハリウェットキャスト法に於て再湿液による塗被
層の可塑化を容易にし、従って、ピンホール状の斑点、
光沢ムラ等の発生をともなうことなく高速で操業可能と
し、かつ、表面強度も強いキャスト紙を製造することを
目的とするものである。In the Hariwet casting method of the present invention, the re-wetting solution makes it easy to plasticize the coating layer, thus eliminating pinhole-like spots.
The purpose of this paper is to produce cast paper that can be operated at high speed without causing uneven gloss, and has a strong surface strength.
本発明者等は、高品質の中ヤストコート紙を高速度で製
造する方法について鋭意研究し九結果、塗被層温度がキ
ャスト塗被液に添加するラテックスのガラス転移温度(
T、G、)−)−50℃を越えない温度条件下で塗被層
を乾燥し、再湿液で再湿潤し死後ラテックスのτ、G、
+30℃を越える温度に加熱したキャスト・ドラムに圧
接してキャスト仕上することによシ、高速度で表面強度
の強い品質のキャスト紙を製造しうること見出し本発明
をなすに至った。The present inventors have conducted extensive research on a method for producing high-quality medium cast coated paper at high speed, and have determined that the coating layer temperature is the glass transition temperature of the latex added to the cast coating liquid.
T, G, )-) The coated layer is dried under a temperature condition not exceeding -50°C, re-wetted with a re-wetting solution, and the post-mortem latex τ, G,
The present inventors have discovered that high-quality cast paper with high surface strength can be produced at high speed by press-contacting the paper to a cast drum heated to a temperature exceeding +30° C., thereby achieving the present invention.
本発明に、顔料、接着剤及び助剤を主成分とする塗被層
を乾燥后再湿潤し、加熱された鏡面ドラムに圧接して強
光沢仕上げするキャストコート紙の製造方法において、
T、G(ガラス転移温度)が20℃以上のラテックスを
全ラテックスのうちの30憾以上接着剤として含有する
塗被液を原紙に塗被層、塗膜の温度がラテックスのT、
G+30℃を越えない条件で乾燥し、再湿潤した后、T
、G+50℃を越える温度望ましくはT、G+50℃以
上に加熱されたキャスト・ドラムに圧接して仕上げるキ
ャスト・コート紙の製造方法である。The present invention provides a method for producing cast coated paper, in which a coating layer mainly composed of pigments, adhesives, and auxiliary agents is re-wetted after drying, and is pressed against a heated mirror drum to give a high gloss finish.
A coating layer is coated on the base paper with a coating liquid containing 30 or more latexes with a glass transition temperature of 20° C. or more as an adhesive out of all the latexes, and the temperature of the coating film is T of the latex.
After drying and rewetting at temperatures not exceeding G+30°C, T
, G + 50° C. or higher, preferably T, G + 50° C. or higher, and press-contacts the paper to a cast drum for finishing.
以下、本発明の詳細な説明する。The present invention will be explained in detail below.
本発明においてに、ラテックスとしてスチレン−ブタジ
ェン重合体、メチルメタクリレート−ブタジェン共重合
体等の共役ジエン系重合体ラテックス、アクリル酸エス
テル及び/又にメタクリル酸エステルの重合体又は共重
合体等のアクリル系重合体ラテックス、エチレン−酢酸
ビニル共重合体等のビニル系重合ラテックス或いはこれ
らの各種重合体をカルボキシルMeの官能基含有単量体
により官能基変性し次アルカリ溶解性、或いはアルカリ
非溶解性の重合体ラテックスのうちT、Gが20℃以上
のラテックス或イd、T、G i 2つ以上有するラテ
ックスに於ては1つ以上のT、Gが20℃以上のラテッ
クスを単独で又は併°用して、あるいは更に下記の接着
剤と併用してキャスト塗被液に添加使用する。In the present invention, the latex may be a conjugated diene polymer latex such as a styrene-butadiene polymer or a methyl methacrylate-butadiene copolymer, or an acrylic latex such as a polymer or copolymer of an acrylic acid ester and/or a methacrylic acid ester. Polymer latex, vinyl polymer latex such as ethylene-vinyl acetate copolymer, or various polymers thereof are functionally modified with a monomer containing a carboxyl Me functional group, and then alkali-soluble or alkali-insoluble polymers are prepared. Among the combined latexes, latexes with T and G of 20°C or higher, or latexes with two or more of d, T, and Gi, use one or more latexes with T and G of 20°C or higher alone or in combination. It can be added to a cast coating solution, or in combination with the following adhesives.
上記ラテックスと併用される接着剤としてはカゼイン、
大豆蛋白、合成蛋白等の蛋白質、陽性澱粉、酸化澱粉等
の澱粉類、カルボ中ジメチルセルロース、ヒドロキシエ
チルセルロース等のセルロース誘導体、ホリビニルアル
コール、オレフィン−無水マレイン酸共重合樹脂、′メ
ラミン樹脂等の合成樹脂系接着剤、スチレン−ブタジェ
ン重合体、メチルメタクリレート−ブタジェン共重合体
等の共役ジエン系重合体ラテックス、アクリル酸エステ
ル及び/又にメタクリル酸エステルの重合体又は、共重
合体等のアクリル系重合体ラテックス、エチレン−酢酸
ビニル共重合体等のビニル系重合ラテックス或いはこれ
らの各種重合体をカルホキクル基等の官能基含有単量体
により官能基変性したアルカリ溶解性、或いはアルカリ
非溶解性の重合体ラテックスのうちT、Gが20℃以下
のラテックス等を用いうる。Adhesives used in combination with the above latex include casein,
Synthesis of proteins such as soybean protein and synthetic proteins, starches such as positive starch and oxidized starch, cellulose derivatives such as dimethyl cellulose and hydroxyethyl cellulose, hollyvinyl alcohol, olefin-maleic anhydride copolymer resin, and melamine resin, etc. Resin adhesives, conjugated diene polymer latex such as styrene-butadiene polymer, methyl methacrylate-butadiene copolymer, acrylic polymer such as acrylic ester and/or methacrylic ester polymer or copolymer Polymer latex, vinyl polymer latex such as ethylene-vinyl acetate copolymer, or alkali-soluble or alkali-insoluble polymers obtained by functionally modifying various polymers thereof with functional group-containing monomers such as carphocyclyl groups. Among latexes, latexes in which T and G are 20° C. or less may be used.
T、Gが20℃以上或いにT、Gを2つ以上有するラテ
ックスに於てrllつ以上のT、Qが20℃以上のラテ
ックス1j:T、Gが20℃以下のラテックス及び/又
はカゼイン、大豆蛋白等のタン白、澱粉等と併用する場
合にij、T、Gが20℃以上のラテックス或いd、T
、Gft2つ以上有するラテックスで1つ以上の?、G
が20℃以上のラテックスの全ラテックスに占める割合
は30係以上とすることが望ましい。Latex with T and G of 20°C or higher or two or more of T and G, including latex with two or more T and Q of 20°C or higher 1j: Latex and/or casein with T and G of 20°C or lower , latex with ij, T, G of 20℃ or higher when used in combination with protein such as soybean protein, starch, etc., or d, T.
, one or more latex with two or more Gft? ,G
It is desirable that the ratio of latex having a temperature of 20°C or higher to the total latex is 30% or higher.
接着剤は、顔料100重量部当シ5〜50重量部、一般
には10〜30重量部の範囲で使用される。又、ラテッ
クスの構造としては、均質構造、断続構造、連続2層構
造その他どのような構造のものを用いてもよい。The adhesive is used in an amount of 5 to 50 parts by weight, generally 10 to 30 parts by weight, per 100 parts by weight of the pigment. Further, the structure of the latex may be a homogeneous structure, an intermittent structure, a continuous two-layer structure, or any other structure.
又、本発明は、上記ラテックスを含む塗被液に助剤とし
てアルミニウム、マグネシュウム、亜鉛の硫酸塩、硝酸
塩、酢酸塩、又はギ酸塩を少なくとも一種含有せしめ、
ラテックスのT、G+30℃以下の温度で乾燥層再湿潤
し、ラテックスのT、G+30℃以上温度に望ましくは
T、G+50℃以上の温度に加熱され念キャスト・ドラ
ムに圧接して仕上げる方法も、含むものである。又、本
発明に於ては再湿潤液の組成に無関係に効果を発揮する
。Further, the present invention includes at least one kind of sulfate, nitrate, acetate, or formate of aluminum, magnesium, or zinc as an auxiliary agent in the coating liquid containing the latex,
It also includes a method of rewetting the dry layer at a temperature of latex T, G + 30°C or lower, heating the latex to a temperature of T, G + 30°C or higher, preferably T, G + 50°C or higher, and pressing it against a cast drum for finishing. It is something that Furthermore, the present invention exhibits its effects regardless of the composition of the rewetting liquid.
リウェツト・キャスト法に於ては、塗被液を塗被−乾燥
層に再湿液で再湿潤し、加熱ドラムに圧接して仕上げる
が、再湿温石の塗被層の可塑化をいかに容易にするか又
、いかにドラムへの密着性を容易にするかが問題となシ
、前述のごとく、再湿潤液の種類を変えたり、乾燥層の
塗被層を平滑にしたシ、あるいは塗被液に凝固剤を添加
し九〕シて問題の解決t−はかることが検討されている
が、本発明者等はこの問題を根本的に解・決するために
ラテックスの持つ造膜の性質を検討し効果のある方法を
見出した。In the rewet casting method, the coated-dry layer is rewetted with a rewetting solution and finished by being pressed against a heated drum. Also, the problem is how to make the adhesion to the drum easier.As mentioned above, it is necessary to change the type of rewetting liquid, smoothen the coating layer of the dry layer, or change the coating liquid. Although it has been considered to solve the problem by adding a coagulant to the latex, the present inventors investigated the film-forming properties of latex in order to fundamentally solve this problem. I found a method that works.
すなわち、ラテックスはラテックス個有の造膜温度を有
し、造膜温度以下では皮膜を作らないという性質に注目
した。That is, latex has its own film-forming temperature, and we focused on the property that it does not form a film below the film-forming temperature.
ラテックスのガラス転移温度(T、G)はポリマーのセ
グメントがガラス状がらゴム状態へ移る点であり、T、
Gを越え九温度でラテックスを乾燥すると、ドライ強度
、耐水性が発現され始め、被膜も部分的に出来る。τ、
Gft越えてさらに温度を上昇して行くに従ってドライ
強度、耐水性は大となシ、造膜μよシ進むが完全な被膜
を形成するにに時間と温度と圧力が影響すると考えられ
る。従って塗工層がラテックスのT、G+30℃以下の
温度になるような乾燥条件で塗工層を乾燥すれば通常の
塗工紙製造における乾燥時間であれば、塗工層中のラテ
ックスは完全な皮膜とならずにドライ強度は弱く、耐水
性も発揮されずそのため再湿液で再湿する時に塗被層は
容易に可塑化され得るものと推定される。The glass transition temperature (T, G) of latex is the point at which the segments of the polymer transition from a glassy state to a rubbery state;
When latex is dried at a temperature exceeding G9, dry strength and water resistance begin to develop, and a film is partially formed. τ,
As the temperature is further increased beyond Gft, the dry strength and water resistance increase, and the film formation μ increases, but it is thought that time, temperature, and pressure influence the formation of a complete film. Therefore, if the coating layer is dried under drying conditions such that the temperature of the coating layer is below T and G of the latex + 30°C, the latex in the coating layer will be completely removed if the drying time is normal for coated paper manufacturing. It does not form a film, has low dry strength, and does not exhibit water resistance, so it is presumed that the coated layer can be easily plasticized when rewetting with a rewetting solution.
再湿後にTO+30℃以上の温度に加熱されたキャスト
・ドラムに圧接すると、ラテックスは熱を受け、皮膜の
形成が進み、面質の良いキャスト・コート紙となり、又
、ラテックスの皮膜形成によシ、塗被層の表面強度も十
分に発揮される。When the latex is pressed against a cast drum heated to a temperature of TO + 30°C or higher after rewetting, the latex receives heat and forms a film, resulting in cast coated paper with good surface quality. The surface strength of the coating layer is also fully demonstrated.
顔料としては、例えば、クレー、カオリン、水酸化アル
ミニウム、炭酸カルシュウA1酸化チタン、硫酸バリウ
ム、酸化亜鉛、サテンホワイト、プラスチックピグメン
ト等、一般の塗被紙用顔料が用いられる。As the pigment, common pigments for coated paper such as clay, kaolin, aluminum hydroxide, calshu carbonate A1 titanium oxide, barium sulfate, zinc oxide, satin white, and plastic pigments are used.
又、助剤として、亜鉛、アルミニウム、マグネシュウム
の硫酸塩、硝酸塩、酢酸塩又はギ酸塩等の塩類を用いて
も良い。Further, as an auxiliary agent, salts such as sulfates, nitrates, acetates, or formates of zinc, aluminum, and magnesium may be used.
ま之、消泡剤、着色剤、流動変性剤、離型剤等の各種助
剤を必要に応じて適宜使用出来る。However, various auxiliary agents such as antifoaming agents, coloring agents, flow modifiers, and mold release agents can be used as appropriate.
本発明においては塗被液は一般に塗被紙製造に用いられ
るブレードコーター、エアーナイフコーター、ロールコ
ータ+、フラV*−1−、カーテンコーター、チャンプ
レックスコーター、バーゴーター、グラビアコーター、
サイズブレスフ−ター等の塗被装置を設けたオンマシン
或いはオフマシンコーターによって、原紙上に一層或い
に、多層に分けて塗被される。In the present invention, the coating liquid is a blade coater, air knife coater, roll coater +, Fura V*-1-, curtain coater, champlex coater, bar coater, gravure coater, etc., which are generally used in the production of coated paper.
The base paper is coated in one layer or in multiple layers using an on-machine or off-machine coater equipped with a coating device such as a size breather footer.
その際の塗被組成物の固形分濃度は、一般に35〜70
重量係であるが、操業性を考慮すると45〜65重量係
の範囲の量が好ましい。At that time, the solid content concentration of the coating composition is generally 35 to 70.
Although it is based on weight, an amount in the range of 45 to 65 weight is preferable in consideration of operability.
原紙としては一般の印刷用塗被紙やキャスト塗被紙に用
いられる米坪30〜40017m”のペーパーペース或
いはポードベースの原紙カ用いられる。これらは、酸性
或いは、アルカリ性抄紙法で抄紙される原紙であシ、高
歩留パルプを約10重量係以上含む中質原紙も勿論使用
出来る。また予備塗工あるいに、キャスト塗被層の裏面
に一般の顔料コーティングを設は念ような塗被紙も原紙
として使用可能″′Cのる。The base paper used is paper pace or pod-based base paper with a weight of 30 to 40,017 m, which is used for general printing coated paper and cast coated paper.These base papers are made using acidic or alkaline papermaking methods. Of course, medium-quality base paper containing high-yield pulp of about 10% or more by weight can also be used.Also, pre-coated or coated paper with a general pigment coating on the back side of the cast coating layer can be used. Can also be used as base paper.
かかる原紙への塗被組成物の塗被量に、乾燥重量で10
〜5017m”程度であるが、得られるキャスト塗被紙
の白紙品質、キャスト塗被速度の改良効果の点で15〜
3517m”の範囲で調節されるのが最も好ましい。The coating amount of the coating composition on such base paper is 10% by dry weight.
〜5017 m'', but in terms of improving the quality of the resulting cast coated paper and the cast coating speed, it is 15~
Most preferably, it is adjusted within a range of 3517 m''.
リウェツト−キャスト法では原紙上に塗被され念塗被組
成物を一旦乾燥するが、その乾燥に ゛は、熱風ドライ
ヤー、エアーホイルドライヤー、エアーギャップドライ
ヤー、シリンダードライヤー、赤外線ドライヤー、電子
線ドクイヤー等通常の塗被紙用乾燥装置が使用される。In the rewet casting method, the final coating composition is coated onto the base paper and dried once, and the drying process is usually carried out using a hot air dryer, air foil dryer, air gap dryer, cylinder dryer, infrared dryer, electron beam dryer, etc. Drying equipment for coated paper is used.
塗被紙の乾燥程度は原紙の種類、塗被組成物の種類等に
よって異なるが、一般に紙水分として1〜15%程度、
よシ好ましくは5〜10暢程度の範囲に乾燥される。乾
燥時の塗被層の温度は前記のとお)ラテックスのT、G
+lO℃を越えないように注意深く乾燥する。The degree of drying of coated paper varies depending on the type of base paper, the type of coating composition, etc., but generally the paper moisture content is about 1 to 15%.
It is preferably dried to a dryness of about 5 to 10 degrees. The temperature of the coating layer during drying is as described above) Latex T, G
Dry carefully not to exceed +10°C.
乾燥后の塗被紙に、必要に応じてマシンキヤノンダー、
スーパーキャレンダー等の”F flt 化処理が行わ
れるが、キャスト塗被紙の特徴である嵩高さや硬度を著
しく損なうような過度の処理に当然避ける必要がある。After drying, apply a machine canonder to the coated paper as needed.
Although "F flt" processing such as super calender is carried out, it is necessary to avoid excessive processing that significantly impairs the bulk and hardness characteristic of cast coated paper.
そして、通常のりウェットキャスト法に従って、塗被層
を再湿潤し、加熱された鏡面ドラムに圧接して強光沢仕
上されるものであるが、本発明の方法に特に鏡面ドラム
を塗被液に使用するラテックスのT、GOうち最も高い
T、G+50℃以上よシ好ましくdT、G+50℃以上
の温度にしてキャスト仕上する。The coating layer is then re-wetted according to the normal glue wet casting method and pressed against a heated mirror drum to achieve a strong gloss finish. In the method of the present invention, the mirror drum is particularly used as the coating liquid. Casting is finished at a temperature of dT, G + 50°C or higher, preferably dT, G + 50°C or higher, which is the highest of T and GO of the latex.
なお、再湿潤液については特に限定されるものではなく
、例えば清水、温水、熱水、離型剤を含有し死水溶液、
ジシアンジアミド尿素等アミン類を含有する水溶液等通
常の再湿潤液が用いられる。Note that the rewetting liquid is not particularly limited, and includes, for example, fresh water, hot water, hot water, a dead water solution containing a mold release agent,
Conventional rewetting fluids such as aqueous solutions containing amines such as dicyandiamide urea are used.
以下に実施例を挙げて本発明をとり具体的に説明するが
、勿論これらに限定されるものではない。なお、列中の
部及び%は特に断らない限シそれぞれ、重量部及び重量
sl示す。The present invention will be specifically explained below with reference to Examples, but it is of course not limited to these. Note that parts and percentages in the columns indicate parts by weight and weight sl, respectively, unless otherwise specified.
実施例1〜4、比較例1〜3
カオリン80部、軽質炭カル20部、ポリアクリル酸ソ
ーダ(14部をセリ二社製プリッタ−を用いて水中に分
散し、固形分濃度55憾の顔料スラリーを調成し九。Examples 1 to 4, Comparative Examples 1 to 3 80 parts of kaolin, 20 parts of light carbon, and 14 parts of sodium polyacrylate were dispersed in water using a splitter manufactured by Serini, and a pigment with a solid content concentration of 55. Prepare slurry 9.
これに消泡剤としてトリブチル7オスフエート14部、
接着剤としてアンモニアを用いて溶解した15%のカゼ
イン水溶液10部(固形分)及び第1表に示すラテック
スを加え、更に離型剤トシてポリエチレンワックスエマ
ルジョン1.5部(固形分)t−0加え、最后にアンモ
ニア及び水を加えて固形分−度を45係、pHを9.5
に調節して6種類の塗被液を得た。In addition to this, 14 parts of tributyl 7 phosphate as an antifoaming agent,
10 parts (solid content) of a 15% casein aqueous solution dissolved using ammonia as an adhesive and the latex shown in Table 1 were added, and a release agent was added to form a polyethylene wax emulsion of 1.5 parts (solid content) t-0. Finally, ammonia and water were added to bring the solid content to 45 and the pH to 9.5.
Six types of coating liquids were obtained.
この塗被液を用いて第1図に示す装置によってリウェツ
トキャストを行った。即ち、米坪60 f/yH”の原
紙1に乾燥重量が25 f/wr”となるように上記塗
被液をクールコーター2で塗被し、乾燥機3で第1表に
示すような条件下で水分が6csになるように乾燥した
。次いでゴムロール4とクロムメツキし九キャストード
ラム5で形成されるプレスニップ6に通紙しここでノズ
ル7から供給された再湿潤液で塗被層表面を再湿潤し之
后、第1表に示すドラム温度条件で回転スピード100
m/分のキャスト・ドラム5にプレス圧150 kg/
cnsで圧接し、乾燥后テークオフ・ロール8でキャス
ト・ドラムから剥離してキャスト塗被紙9t−製造した
。得られたキャスト塗被紙の品質を第1表に示す。Using this coating liquid, rewet casting was performed using the apparatus shown in FIG. That is, the above coating liquid was applied to base paper 1 with a dry weight of 60 f/yH'' using a cool coater 2 so that the dry weight was 25 f/wr'', and the coating was applied in a dryer 3 under the conditions shown in Table 1. It was dried at the bottom to a moisture content of 6 cs. Next, the paper is passed through a press nip 6 formed by a rubber roll 4 and a chrome-plated cast drum 5, where the surface of the coated layer is re-wetted with a re-wetting liquid supplied from a nozzle 7, and then the drum shown in Table 1 Rotation speed 100 under temperature conditions
Pressing pressure 150 kg/min on cast drum 5
The paper was pressed with cns, and after drying, it was peeled off from the cast drum with a take-off roll 8 to produce 9 tons of cast coated paper. Table 1 shows the quality of the cast coated paper obtained.
表面性及び白紙光沢度の測定に下記のとおシとしな。Follow the instructions below to measure surface properties and white paper gloss.
〔表面性〕 O・・・良好
(表面欠陥) Δ・ ・ ・やや良好×・・・不良
〔白紙光沢] グロスメーター(75°)で測定。(日
本電色工業LLoVG
−10型グロスメーター)
実施例5〜6.比較例4〜5
カオリン80部、軽質炭カル20部、ポリアクリル酸ソ
ーダ(14部をセリ二社製プリッタ−を用いて水中に分
散し、固形分濃度55係の顔料スラリーを調成した。[Surface properties] O...Good (surface defects) Δ... Slightly good ×...Poor [White paper gloss] Measured with a gloss meter (75°). (Nippon Denshoku Kogyo LLoVG-10 type gloss meter) Examples 5 to 6. Comparative Examples 4 to 5 80 parts of kaolin, 20 parts of light coal, and 14 parts of sodium polyacrylate were dispersed in water using a splitter manufactured by Serini Co., Ltd. to prepare a pigment slurry with a solid content concentration of 55.
これに消泡剤としてトリブチル7オスフエートα4部、
接着剤として、アンモニアを用いて溶解した15esの
カゼイン水溶液10部(固形分)及び第2表に示すラテ
ックスを加え、次に離型剤としてボリエ、チVンワック
スエマルジョン1.5部(固形分)を加え、更に助剤と
して、硫酸亜鉛の10%水溶液を13係(固形分)を添
加し、−鍛冶に、アンモニア及び水を加えて固形分濃度
t−45憾、pHft、9.5に調節して4種類の塗被
液を得た。In addition, 4 parts of tributyl 7-osphate α as an antifoaming agent,
As an adhesive, 10 parts (solid content) of a 15es casein aqueous solution dissolved using ammonia and the latex shown in Table 2 were added, and then 1.5 parts of Bolier and Chin Vine wax emulsion (solid content) were added as a release agent. ), and further added 10% aqueous solution of zinc sulfate (solid content) as an auxiliary agent, and then added ammonia and water to the forge to a solid content concentration of t-45 and pH ft of 9.5. Adjustments were made to obtain four types of coating liquids.
この塗被液を用いて第1図に示す装置によってリウェツ
ト・キャストを行った。即ち、米坪6017m” (D
K紙I K乾燥f[jl125t/、* トなるよう
に上記塗被液をロールコータ−2で塗被し、乾燥機3で
第2表に示すよダな条件下で水分が6%になるように乾
燥した。次いでプレス・ロール4とのクロムメツキした
キャスト・ドラム5で形成されるプレス・ニップ6に通
紙し、ここでノズル7から供給された再湿液で塗被層表
面を再湿潤した后、第2表に示すドラム温度条件で回転
スピード100m/分のキャスト・ドラム5にプレス圧
15’ Oky / cpsで圧接し、乾燥后テークオ
フ・四−ル8でキャスト・ドラムから剥離してキャスト
塗被紙9を製造した。Using this coating liquid, rewet casting was performed using the apparatus shown in FIG. In other words, 6017m” (D
K paper I K drying f [jl125t/, * Coat the above coating liquid with roll coater 2 so that the moisture content becomes 6% in dryer 3 under the better conditions shown in Table 2. So dry. The paper is then passed through a press nip 6 formed by a chrome-plated cast drum 5 with a press roll 4, where the surface of the coating layer is rewetted with a rewetting liquid supplied from a nozzle 7, and then a second Under the drum temperature conditions shown in the table, it was pressed against a cast drum 5 at a rotation speed of 100 m/min at a press pressure of 15'Oky/cps, and after drying, it was peeled off from the cast drum using a take-off four-wheel 8 to form a cast coated paper 9. was manufactured.
得られ念キャスト塗被紙の品質を第2表に示す。The quality of the obtained cast coated paper is shown in Table 2.
〔発明の効果]
各実施列の結果から明らかなように、本発明の方法でに
、先に記述したように、再湿潤液で再湿する時に塗被層
に容易に可塑イヒされ、キャスト・ドラムに密着性が良
く従って欠陥の少ないキャスト面が得られる。又塗被液
に助剤(アルミニウム、マグネシュウム、カルシウム、
亜鉛の硫酸塩、硝酸塩、酢酸塩又はギ酸塩)を使わなく
ても良いし、或いは少量の添加で良いため塗被層の表面
強度に弱くならない利点カニある。[Effects of the Invention] As is clear from the results of each series of implementations, the method of the present invention can easily plasticize the coating layer when rewetting with the rewetting solution as described above, making it easier to cast. A cast surface with good adhesion to the drum and fewer defects can be obtained. Also, auxiliary agents (aluminum, magnesium, calcium,
It has the advantage that it does not require the use of zinc sulfates, nitrates, acetates or formates, or only requires the addition of a small amount, so the surface strength of the coating layer is not weakened.
従って、再湿法キャストニ、本発明によシ容易に実施出
来、キャスト・スピードも大巾に上げることが出来る。Therefore, the rewetting method of casting can be easily carried out according to the present invention, and the casting speed can be greatly increased.
第1図は本発明を実施するための装置のフロー概略図を
示す。
1・・・原Wc、2−・ロールコーjl−15・−・乾
燥WA、4−・・プレスロール、5−・・キャストドラ
ム、6−・・プレスニップ、8・・・テークオフ0−ル
、9・−キャスト塗被紙
手 続 補 正 書
昭和65年3月25日
特許庁長官 小 川 邦 夫 殿
1、事件の表示 昭和62年特許頼第291727号
λ発明の名称 キャストコート紙の製造方法五補正を
する者
事件との関係 特許出願人
住 所 東京都中央区銀座4丁目7番5号名 称 王
子製紙株式会社
代表者 河 毛 二 部
1補正命令の日付 自発補正
&補正の対象
2補正の内容
(1) 明細書6頁18行〜19行の「或いは一一一
ラテックス」を削除する。
(2)同6頁20行の「を単独で又は併用して、あるい
は更に」を「を単独で、又Itt4 を楠り1゜(3)
同7頁末行〜8頁2行の「或いは一−−−T、Gが20
℃以上」を削除する。
(4)同8頁5行〜7行の「或いは、T、G−−−−T
、Gが20℃以上のラテックス」を削除する。
(5)同8頁11行〜13行の「又、ラテックスの構造
としては、−一一一を用いていてもよい。」を削除する
。
(6)同14頁8行の「実施例1〜4」を「実施例1〜
3」と補正する。
(7)同16頁表1中の「〃3」の欄(実施例30tm
>を削除し、「14」を「13」と補正する。
(8)同17頁9行の「実施例5〜6」を「実施例4〜
5」と補正する。
(9)同19頁第2表の「実施例5」を「実施例4」と
補正し、「〃6」を「〃5」と補正する。FIG. 1 shows a flow diagram of an apparatus for carrying out the invention. 1... Raw Wc, 2-... Roll roll jl-15... Drying WA, 4-... Press roll, 5-... Cast drum, 6-... Press nip, 8... Take-off 0-roll, 9.-Cast Coated Paper Procedures Amendment Written on March 25, 1986 Kunio Ogawa, Commissioner of the Patent Office 1. Indication of the case Patent Request No. 291727 of 1988 λ Name of the invention Method for manufacturing cast coated paper 5 Relationship with the case of the person making the amendment Patent applicant Address 4-7-5 Ginza, Chuo-ku, Tokyo Name Oji Paper Co., Ltd. Representative Kawage 2 Date of Part 1 amendment order Voluntary amendment & Subject of amendment 2 Amendment Contents (1) Delete "or 111 latex" on page 6, lines 18 and 19 of the specification. (2) On page 6, line 20, change “alone or in combination, or in addition” to “alone, or Itt4” 1゜(3)
From the last line of page 7 to line 2 of page 8, “or one---T, G is 20
℃ or more” is deleted. (4) On page 8, lines 5 to 7, “Or, T, G---T
, Latex with G of 20°C or higher" is deleted. (5) Delete "Also, -111 may be used as the structure of latex" in lines 11 to 13 of page 8. (6) Change “Examples 1 to 4” on page 14, line 8 to “Examples 1 to 4”
3”. (7) Column “3” in Table 1 on page 16 (Example 30tm
> and correct "14" to "13". (8) Change “Examples 5 to 6” on page 17, line 9 to “Examples 4 to 6”
5”. (9) In Table 2 on page 19, "Example 5" is corrected to "Example 4" and "〃6" is corrected to "〃5".
Claims (1)
後再湿潤し、加熱された鏡面ドラムに圧接して強光沢仕
上げするキャストコート紙の製造方法において、ガラス
転移温度が 20℃以上のラテックスを全ラテックスの 30重量%以上含有するラテックスを接着剤として含有
する塗被液を原紙に塗被した後、塗膜の温度がラテック
スのガラス転移温度+30℃を越えない条件で乾燥し、
再湿潤した後ガラス転移温度+30℃以上の温度に加熱
されたキャスト・ドラムに圧接することを特徴とするキ
ャストコート紙の製造方法。[Scope of Claims] 1. A method for manufacturing cast coated paper, in which a coated layer mainly composed of pigments, adhesives, and auxiliary agents is dried, re-wetted, and then pressed against a heated mirror drum to give a strong gloss finish. After coating a base paper with a coating liquid containing latex as an adhesive containing 30% by weight or more of the total latex with a glass transition temperature of 20°C or higher, the temperature of the coating film is the glass transition temperature of the latex + 30°C. Dry under conditions not exceeding
A method for producing cast-coated paper, which comprises press-contacting the paper to a cast drum heated to a glass transition temperature +30° C. or higher after being re-wetted.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62291727A JPH0674558B2 (en) | 1987-11-20 | 1987-11-20 | Cast coated paper manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62291727A JPH0674558B2 (en) | 1987-11-20 | 1987-11-20 | Cast coated paper manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01139895A true JPH01139895A (en) | 1989-06-01 |
JPH0674558B2 JPH0674558B2 (en) | 1994-09-21 |
Family
ID=17772614
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62291727A Expired - Fee Related JPH0674558B2 (en) | 1987-11-20 | 1987-11-20 | Cast coated paper manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0674558B2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54125712A (en) * | 1978-03-17 | 1979-09-29 | Mitsubishi Paper Mills Ltd | Production of high glazed coated paper |
JPS60146097A (en) * | 1983-12-29 | 1985-08-01 | 神崎製紙株式会社 | Production of cast coated paper |
-
1987
- 1987-11-20 JP JP62291727A patent/JPH0674558B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54125712A (en) * | 1978-03-17 | 1979-09-29 | Mitsubishi Paper Mills Ltd | Production of high glazed coated paper |
JPS60146097A (en) * | 1983-12-29 | 1985-08-01 | 神崎製紙株式会社 | Production of cast coated paper |
Also Published As
Publication number | Publication date |
---|---|
JPH0674558B2 (en) | 1994-09-21 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |