JP2717177B2 - Manufacturing method of lightweight cast coated paper - Google Patents
Manufacturing method of lightweight cast coated paperInfo
- Publication number
- JP2717177B2 JP2717177B2 JP62035795A JP3579587A JP2717177B2 JP 2717177 B2 JP2717177 B2 JP 2717177B2 JP 62035795 A JP62035795 A JP 62035795A JP 3579587 A JP3579587 A JP 3579587A JP 2717177 B2 JP2717177 B2 JP 2717177B2
- Authority
- JP
- Japan
- Prior art keywords
- cast
- pigment
- coated paper
- coating
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000000576 coating method Methods 0.000 claims description 48
- 239000011248 coating agent Substances 0.000 claims description 46
- 239000000049 pigment Substances 0.000 claims description 25
- 239000011230 binding agent Substances 0.000 claims description 19
- 238000010521 absorption reaction Methods 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 14
- 239000010410 layer Substances 0.000 description 26
- 230000035699 permeability Effects 0.000 description 14
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 238000005266 casting Methods 0.000 description 8
- 230000007547 defect Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 239000005995 Aluminium silicate Substances 0.000 description 4
- 239000005909 Kieselgur Substances 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 235000012211 aluminium silicate Nutrition 0.000 description 4
- 239000011247 coating layer Substances 0.000 description 4
- 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 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- -1 satin white Chemical compound 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 229920002472 Starch 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
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 230000001965 increasing effect Effects 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000004078 waterproofing Methods 0.000 description 2
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- 241000257465 Echinoidea Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black 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
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- PGZIKUPSQINGKT-UHFFFAOYSA-N dialuminum;dioxido(oxo)silane Chemical compound [Al+3].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O PGZIKUPSQINGKT-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Thermal Transfer Or Thermal Recording In General (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Paper (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Color Printing (AREA)
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は軽量キャストコート紙に関するものである。
(従来の技術)
従来、キャストコート紙は湿潤状態のコーティング層
を加熱ドラム面に圧接して光沢仕上げするウェットキャ
スト法,湿潤状態のコーティング層をゲル状態にして加
熱ドラム面に圧接して光沢仕上げするゲル化キャスト
法、湿潤状態のコーティング層を一旦乾燥又は半乾燥し
た後再湿潤により可塑化で加熱ドラム面に圧接するリウ
ェットキャスト法等によって製造されている。また原紙
上に顔料及び結着剤を主体とする下塗り層を形成した後
に、上塗り層を形成しこの上塗り層が湿潤状態にある間
に加熱ドラム面に圧接して光沢仕上げする方法も提案さ
れている。
(発明が解決しようとする問題点)
これらのキャスト法はいづれも湿潤状態にある顔料及
び結着剤を主成分とするコーティング層を加熱ドラム面
に圧接乾燥後剥離する点で共通しており、塗布量は一般
に15〜35g/m2であり、塗工速度は直径3.6mのドラムドラ
イヤーを用いた場合50m/min前後と低速であり、本発明
者等が確認したところ、高速で乾燥するとキャスト表面
にピンホール等を生じ不満足な表面となることが判明し
た。
(問題点を解決するための手段)
本発明者等は表面性良好なキャストコート紙を高速で
製造すべく鋭意検討した結果本発明を完成するに到っ
た。
すなわち、本発明は
1.紙支持体上に、顔料及び結着剤を主成分とし、吸油
量(JIS K5101)50m1/100g以上の顔料を10〜80重量%含
有するアンダーコート層を設けた、透気度(JIS P811
7)300秒以下の基紙上に、顔料、熱可融性物質及び結着
剤を主成分とするキャストコート層を設けることを特徴
とする軽量キャストコート紙の製造方法。
2.キャストコート層の塗布量が0.5〜10g/m2であるこ
とを特徴とする上記1記載の軽量キャストコート紙の製
造方法。
3.キャストコート層の主成分が、顔料20〜60重量%、
熱可融性物質10〜50重量%、結着剤10〜40重量%である
ことを特徴とする上記1または2記載の軽量キャストコ
ート紙の製造方法。
である。
アンダーコート層に使用される顔料としては、カオリ
ン,クレー,炭酸カルシウム,炭酸マグネシウム,酸化
マグネシウム,酸化チタン,酸化亜鉛,水酸化アルミニ
ウム,硫酸バリウム,タルク,サチンホワイト,硫酸カ
ルシウム,シリカなどの無機顔料,ポリスチレン,尿
素,ホルムアルデヒド樹脂,デンプン粒等の有機顔料が
用いられるが、アンダーコート層を設けた基紙の透気度
を300秒以下とするには吸油量(JIS K5101)が50ml/100
g以上の顔料を用いるのが好適であり、該吸油量50ml/10
0g以上の顔料の含有量としてはアンダーコート層重量に
対して10〜80重量%であることが望ましい。10重量%未
満であると透気性が低下し、キャスト塗工時に水分の蒸
発が遅くなり操業速度が低下したり、キャストコート面
にピンホール状の欠陥が発生する。80重量%を越えると
接着性が悪くなり、キャスト塗工時にドラムドライヤー
との剥離が悪くなりドラムドライヤーにカスが付着す
る。
又、吸油量50ml/mg以上の顔料を用いない場合は通気
性が不均一になり通気性の悪い部分はキャストコート塗
液水分の蒸発によってフクレが生じたりピンホール等の
欠陥が発生する。吸油量50ml/mg以上好ましくは80ml/mg
以上の顔料を用いることにより通気性の均一性が保持さ
れキャストコート面の表面性を良好な状態とすることが
できる。
吸油量50ml/mg以上の好ましい顔料としては例えば以
下のようなものがある。但し、( )内数値は吸油量
(ml/100g)を示す。ケイソウ土(110〜210)、焼成ケ
イソウ土(130〜140)、融剤焼成ケイソウ土(120〜16
0)、焼成クレー(50〜57)、天然黒鉛微粉末(50〜10
0)、天然土状黒鉛(50〜120)、カーボンブラック(50
〜150)、ホワイトカーボン(50〜300)、微粒子状無水
シリカ(100〜300)、微粒子状無水酸化アルミニウム
(100〜250)、微粒子状酸化チタン(50〜120)、炭酸
マグネシウム(50〜150)、ケイ酸アルミン酸マグネシ
ウム(300〜340)、顔料を物理的又は化学的に処理して
50ml/100g以上の吸油量を保持せしめるようにしたも
の、例えば針柱状炭酸カルシウム粒子を三次元的に組み
合せてウニ状の形状とし吸油量を60ml/100g以上とした
もの。
又、アンダーコート層に使用される結着剤としては澱
粉,変性澱粉,カゼイン,プロティン,ゼラチン,セル
ロース類,ポリビニルアルコール,変性ポリビニルアル
コール,スチレン,ブタジエン共重合体,スチレン・ア
クリロニトリル共重合体,スチレン・アクリル共重合
体,ポリアクリルアミド等の各種天然及び合成の結着剤
が水溶液又はラテックス,エマルジョンの形で用いられ
る。結着剤は種類によって接着強度が異なるので結着剤
量は面一的ではないが通常塗液固形分の5〜30重量%程
度使用され、通気性を著しく阻害しない程度に顔料相互
間あるいは原紙またはキャストコート層との接着に必要
な最低量で用いるのが良い。
アンダーコート塗液中には必要に応じて分散剤,耐水
化剤,消泡剤,防腐剤,染料,熱可融性物質等が適宜含
有し得るものであり、エアナイフコーター、ブレードコ
ーター、バーコーター、ロールコーター、ブラシコータ
ー、グラビアコーターなどの塗工機によって紙支持体上
に乾燥塗布量3〜10g/m2になるように塗工され、更に必
要に応じてマシンキャレンダー,スーパーキャレンダー
等のキャレンダー処理が施される。アンダーコート塗布
量が3g/m2未満であるとキャストコート紙の表面性が悪
く、又、10g/m2を超えると効果は向上せず生産性が低下
し、経済的にもコストアップし、好ましくない。
アンダーコート層を設けた基紙の透気度(JIS P811
7)は300秒以下好ましくは200秒以下であることが重要
であり、300秒を超えて通気性が悪くなると塗工速度を
低下させないと、十分乾燥できず更にはキャストコート
表面にピンホール等の欠陥が出来表面性が損われる。
キャストコート層に用いられる顔料・結着剤としては
前述のアンダーコート層と同じものが使用できる。熱可
融性物質としてはステアリン酸亜鉛,ステアリン酸カル
シウム等の金属石ケン,カルナパワックス,みつろう,
モンタンワックス等の天然ワックス,パラフィンワック
ス,マイクロワックス等の石油ワックス,ポリエチレン
ワックス,脂肪酸アミド,脂肪酸エステル等の合成物が
使用できる。
顔料,熱可融性物質,結着剤の使用量は夫々使用する
薬品の種類によって性質が異なるので面一的ではない
が、通常、キャストコート塗液組成は乾燥重量として顔
料は20〜60重量%、熱可融性物質は10〜50重量%、結着
剤は10〜40重量%のものが使用される。顔料はインク受
理性、光沢度等を考慮して種類・使用量を決定するが20
重量%より少ないとインク受理性が悪くなり、50重量%
より多過ぎると表面性が悪くなる。熱可融性物質は湿潤
状態で加熱ドラム面に圧接・乾燥されるときキャストコ
ート層の可塑性を増し、低塗布量でも充分良好なキャス
ト表面が得られる。熱可融性物質が10重量%より少ない
とその効果が不充分となり表面性が悪くなり、50重量%
より多過ぎるとインク受理性等が悪くなる。
結着剤は顔料,熱可融性物質の残余であり、各成分を
互いに接着し、アンダーコート層との接着をするに充分
な量が用いられる。
キャストコート塗液中には必要に応じて分散剤,消泡
剤,各種界面活性剤,耐水化剤,防腐剤,染料,螢光顔
料,螢光増白剤等が適宜含有し得るものであり、ウェッ
トキャスト法,リウェットキャスト法,ゲル化キャスト
法等のキャスト法によって乾燥塗布量0.5〜10g/m2にな
るように塗工される。キャストコート塗布量が0.5g/m2
未満ではアンダーコート層表面を埋めきれず表面性が不
充分となり、10g/m2以上では乾燥に時間がかかり塗工速
度が低下する。
(作用及び効果)
本発明のように、紙支持体上に顔料,結着剤を主成分
とするアンダーコート層を設けた基紙の透気度を300秒
以下とし、該基紙上に顔料,熱可融性物質,結着剤を主
成分とするキャストコート層を設けることにより、コー
ト層の塗布量が15g/m2以下の表面性良好な軽量キャスト
コート紙を得ることができ、塗工速度を著しく高めるこ
とができる。
すなわち、本発明はアンダーコート層を設けることに
よりキャストコート表面を良好にするものであり、その
際基紙の透気度を300秒以下とすることによりキャスト
コート塗液の水分が基紙を通過して裏面より蒸発するの
を促進して乾燥性を高めたものであり、更にはキャスト
コート層中に含有した熱可融性物質の可塑性増加効果に
よりキャストコート層の低塗布量化を達成し、乾燥性の
良好な軽量キャストコート紙を提供できるに到ったもの
である。
本発明の軽量キャストコート紙は印刷用紙に用いられ
るだけでなく、アンダーコート層あるいはキャスト層に
用いる薬品を工夫することにより熱転写受容シート、感
圧受容シート、感熱記録シート、インクジェット用記録
紙磁気記録シート用原紙等の情報関連用紙、化粧シート
等への応用が可能であり非常に有用な技術と考えられ
る。
(実施例)
次に本発明を実施例によってさらに具体的に説明する
が、本発明はこれらの実施例の記載に限定されるもので
はない。実施例中の部は固形分の重量部を示す。
実施例1
ケイソウ土(セライトスーパークロス吸油量125:ジョ
ンズマンビル社製)40部、軽質炭酸カルシウム(ソネッ
クスE吸油量40:白石工業(株)製)30部、酸化澱粉(M
S・3800日本食品(株)製)15部、変性アクリル樹脂エ
マルジョン(モビニールL−8010:ヘキスト合成(株)
製)15部からなる固形分濃度35%のアンダーコート塗液
を調製した。
カオリン40部、軽質炭酸カルシウム20部、ステアリン
酸亜鉛15部、ポリビニルアルコール10部、変性アクリル
樹脂エマルジョン15部からなる固形分濃度30%のキャス
トコート塗液を調製した。
第1図に示す装置を用いて、50g/m2の原紙にアンダー
コート塗液を乾燥塗布量6g/m2となるようにエアナイフ
コーターで塗工・乾燥した後、キャストコート塗液を乾
燥塗布量3g/m2となるように塗布し、90℃に加熱された
キャストドラムにてキャスト仕上げを行なった。
このようにして得られた軽量キャストコート紙の表面
は欠陥がなく良好であり、最高塗工速度は150m/minであ
った。尚、アンダーコートを施した基紙の透気度は80秒
であった。
実施例2
実施例1のアンダーコート塗液のケイソウ土を針柱状
炭酸カルシウムの三次元ウニ状粒子(カルライトSA吸油
量60:白石工業(株)製)に、キャストコート塗液のス
テアリン酸亜鉛をパラフィンワックスに代えた以外は実
施例1と同様にして軽量キャストコート紙を得た。この
ようにして得られた軽量キャストコート紙の表面は欠陥
がなく良好であり、最高塗工速度は130m/minであった。
尚、アンダーコートを施した基紙の透気度は200秒であ
った。
比較例1
実施例1においてアンダーコート塗液のケイソウ土を
カオリン(アストラブライト吸油量40:ジョージアカオ
リン社製)に代えた以外は実施例1と同様にして軽量キ
ャストコート紙を作製したが、キャストコート塗液の乾
燥が遅く最高塗工速度は90m/minであり、キャストコー
ト表面にピンホールが目立ち表面性不良であった。表面
性を良好にするにはキャストコート層の乾燥塗布量が10
g/m2以上必要であり、最高塗工速度は60m/min以下にな
った。尚、アンダーコートを施した基紙の透気度は500
秒であった。
比較例2
カオリン(アストラブライト吸油量40)45部、重質炭
酸カルシウム(エスカロン#1500吸油量28:三共精粉
(株)製)20部、ポリビニルアルコール(コーセノール
N−300日本合成化学(株)製)15部、スチレン・ブタ
ジエンラテックス(JSR 0561日本合成ゴム(株)製)20
部からなる固形分濃度45%のアンダーコート塗液を調製
した。このアンダーコート塗液と実施例1のキャストコ
ート塗液を用いて実施例1と同様にして軽量キャストコ
ート紙を作製した。このときのアンダーコートを施した
基紙の透気度は1000秒以上であり、キャストコート塗液
の乾燥が遅く最高塗工速度は40m/minであり、キャスト
ドラム面にキャストコート塗液が部分的に付着し、キャ
ストコート表面の欠陥が著しく多く表面性が劣ってい
た。
比較例3
実施例1においてキャストコート塗液中のステアリン
酸亜鉛を除いた以外は実施例1と同様にして軽量キャス
トコート紙を作製した。このときの最高塗工速度は150m
/minであり、キャストコート表面はピンホール,コート
ムラ等の欠陥が目立った。キャストコート表面を良くす
るにはキャストコート層の乾燥塗布量が10g/m2以上必要
であり最高塗工速度は80m/min以下になった。The present invention relates to a lightweight cast-coated paper. (Prior art) Conventionally, cast-coated paper has a wet coating method in which the wet coating layer is pressed against the heating drum surface to produce a glossy finish. The wet coating layer is made into a gel state and pressed against the heating drum surface to produce a glossy finish. It is manufactured by a gel casting method, a wet coating method in which a wet coating layer is once dried or semi-dried, and then re-wet to plasticize and press against a heating drum surface. Also, a method has been proposed in which after forming an undercoat layer mainly composed of a pigment and a binder on a base paper, a top coat layer is formed, and while this overcoat layer is in a wet state, is pressed against a heating drum surface to perform a gloss finish. I have. (Problems to be Solved by the Invention) These casting methods are common in that a coating layer mainly containing a pigment and a binder in a wet state is peeled off after being pressed against a heating drum surface and dried. the coating amount is generally 15 to 35 g / m 2, coating speed is 50 m / min before and after the low-speed when using the drum dryer with a diameter of 3.6 m, when the present inventors or the like is confirmed, and dried in a high speed casting It was found that pinholes and the like occurred on the surface, resulting in an unsatisfactory surface. (Means for Solving the Problems) The present inventors have made intensive studies to produce cast-coated paper having good surface properties at high speed, and as a result, have completed the present invention. That is, the present invention provides: 1. an undercoat layer containing 10 to 80% by weight of a pigment having a pigment and a binder as main components and an oil absorption (JIS K5101) of 50 m1 / 100 g or more, on a paper support; Air permeability (JIS P811
7) A method for producing a lightweight cast-coated paper, comprising providing a cast coat layer containing pigment, a heat-fusible substance and a binder as main components on a base paper of 300 seconds or less. 2. The method for producing a lightweight cast-coated paper according to the above item 1, wherein the coating amount of the cast coat layer is 0.5 to 10 g / m 2 . 3. The main component of the cast coat layer is pigment 20 ~ 60% by weight,
3. The method for producing a lightweight cast-coated paper according to the above item 1 or 2, wherein the content is 10 to 50% by weight of a heat-fusible substance and 10 to 40% by weight of a binder. It is. Examples of pigments used in the undercoat layer include inorganic pigments such as kaolin, clay, calcium carbonate, magnesium carbonate, magnesium oxide, titanium oxide, zinc oxide, aluminum hydroxide, barium sulfate, talc, satin white, calcium sulfate, and silica. Organic pigments such as polystyrene, urea, formaldehyde resin, starch granules, etc. are used. In order to keep the air permeability of the base paper with an undercoat layer below 300 seconds, the oil absorption (JIS K5101) must be 50 ml / 100.
g or more of the pigment is preferable, and the oil absorption is 50 ml / 10.
The content of the pigment of 0 g or more is desirably 10 to 80% by weight based on the weight of the undercoat layer. If it is less than 10% by weight, the air permeability decreases, the evaporation of water slows down during casting, the operating speed decreases, and pinhole-like defects occur on the cast coat surface. If it exceeds 80% by weight, the adhesiveness becomes poor, the peeling off from the drum dryer during cast coating becomes poor, and scum adheres to the drum dryer. When a pigment having an oil absorption of 50 ml / mg or more is not used, the air permeability becomes non-uniform, and in areas where the air permeability is poor, swelling or defects such as pinholes occur due to evaporation of the cast coat coating solution water. Oil absorption 50ml / mg or more, preferably 80ml / mg
By using the above pigment, the uniformity of air permeability is maintained, and the surface property of the cast coat surface can be improved. Preferred pigments having an oil absorption of 50 ml / mg or more include, for example, the following. However, the values in parentheses indicate the oil absorption (ml / 100g). Diatomaceous earth (110-210), calcined diatomaceous earth (130-140), flux calcined diatomaceous earth (120-16
0), calcined clay (50-57), natural graphite fine powder (50-10
0), natural earth graphite (50-120), carbon black (50
~ 150), white carbon (50 ~ 300), fine anhydrous silica (100 ~ 300), fine anhydrous aluminum oxide (100 ~ 250), fine titanium oxide (50 ~ 120), magnesium carbonate (50 ~ 150) , Magnesium aluminate silicate (300-340), pigment is physically or chemically treated
Those having an oil absorption of 50 ml / 100 g or more, for example, those having needle-column-shaped calcium carbonate particles three-dimensionally combined to form a sea urchin shape and having an oil absorption of 60 ml / 100 g or more. Examples of the binder used in the undercoat layer include starch, modified starch, casein, protein, gelatin, celluloses, polyvinyl alcohol, modified polyvinyl alcohol, styrene, butadiene copolymer, styrene / acrylonitrile copolymer, and styrene. -Various natural and synthetic binders such as acrylic copolymer and polyacrylamide are used in the form of an aqueous solution, latex or emulsion. Since the adhesive strength varies depending on the type of the binder, the amount of the binder is not uniform. However, usually about 5 to 30% by weight of the solid content of the coating liquid is used. Alternatively, it is preferable to use a minimum amount necessary for adhesion to the cast coat layer. The undercoat coating liquid may contain a dispersant, a water-proofing agent, an antifoaming agent, a preservative, a dye, a heat-fusible substance, and the like, as necessary, and may include an air knife coater, a blade coater, and a bar coater. , A roll coater, a brush coater, a gravure coater, etc., coated on a paper support to a dry coating amount of 3 to 10 g / m 2 , and if necessary, a machine calender, a super calender, etc. Is performed. Undercoat coating amount is poor surface properties of the cast-coated paper is less than 3 g / m 2, also effect exceeds 10 g / m 2 was decreased productivity without improvement, also cost economical, Not preferred. Air permeability of base paper with undercoat layer (JIS P811
It is important that 7) is 300 seconds or less, preferably 200 seconds or less, and if the air permeability exceeds 300 seconds, the coating speed cannot be reduced unless the coating speed is reduced. Defects and surface properties are impaired. As the pigment / binder used in the cast coat layer, the same pigments and binders as those described above for the undercoat layer can be used. Examples of the heat-fusible material include metal soaps such as zinc stearate and calcium stearate, carnapa wax, beeswax,
Natural waxes such as montan wax, petroleum waxes such as paraffin wax and micro wax, polyethylene waxes, and synthetic compounds such as fatty acid amides and fatty acid esters can be used. The amount of the pigment, the heat-fusible substance, and the binder is not uniform because the properties vary depending on the type of the chemical used. %, The heat-fusible substance is 10 to 50% by weight, and the binder is 10 to 40% by weight. The type and amount of the pigment are determined in consideration of ink acceptability, glossiness, etc.
If the amount is less than 50% by weight, ink receptivity becomes poor,
If the amount is too large, the surface properties deteriorate. The heat-fusible substance increases the plasticity of the cast coat layer when pressed and dried on the surface of the heating drum in a wet state, and a sufficiently good cast surface can be obtained even with a low coating amount. If the content of the heat-fusible substance is less than 10% by weight, the effect is insufficient and the surface property is deteriorated, and 50% by weight.
If the amount is too large, ink acceptability and the like deteriorate. The binder is a residue of the pigment and the heat-fusible substance, and is used in an amount sufficient to adhere the components to each other and adhere to the undercoat layer. The coating liquid of the cast coat may contain a dispersing agent, a defoaming agent, various surfactants, a water-proofing agent, a preservative, a dye, a fluorescent pigment, a fluorescent brightener, etc. as necessary. It is applied to a dry coating amount of 0.5 to 10 g / m 2 by a casting method such as a wet casting method, a rewetting casting method, and a gelling casting method. 0.5 g / m 2 of cast coat
If less than 10 g / m 2 , drying takes a long time and the coating speed is reduced. (Function and Effect) As in the present invention, the air permeability of a base paper having an undercoat layer containing a pigment and a binder as main components on a paper support is set to 300 seconds or less, and the pigment, By providing a cast coat layer containing a heat-fusible substance and a binder as main components, it is possible to obtain a lightweight cast-coated paper with good surface properties with a coating amount of 15 g / m 2 or less. Speed can be significantly increased. That is, the present invention is to improve the cast coat surface by providing an undercoat layer, in which case the moisture of the cast coat coating solution passes through the base paper by setting the air permeability of the base paper to 300 seconds or less. It promotes evaporation from the back side to enhance the drying property, and further achieves a low coating amount of the cast coat layer by the plasticity increasing effect of the heat fusible substance contained in the cast coat layer, Thus, it is possible to provide a lightweight cast-coated paper having good drying properties. The lightweight cast-coated paper of the present invention is used not only for printing paper, but also for thermal transfer receiving sheets, pressure-sensitive receiving sheets, heat-sensitive recording sheets, and inkjet recording paper magnetic recording by devising chemicals used for undercoat layers or cast layers. It can be applied to information-related paper such as sheet base paper, decorative sheets, etc., and is considered to be a very useful technology. (Examples) Next, the present invention will be described more specifically with reference to examples, but the present invention is not limited to the description of these examples. Parts in the examples indicate parts by weight of the solid content. Example 1 Diatomaceous earth (Celite Supercross Oil Absorption 125: manufactured by Johns Manville Co.) 40 parts, light calcium carbonate (Sonex E oil absorption 40: manufactured by Shiraishi Industry Co., Ltd.) 30 parts, oxidized starch (M
15 parts of S.3800 Nippon Shokuhin Co., Ltd., modified acrylic resin emulsion (Movinyl L-8010: Hoechst Gosei Co., Ltd.)
Co., Ltd.) and an undercoat coating solution having a solid content concentration of 35% was prepared. A cast coat coating liquid having a solid content concentration of 30%, comprising 40 parts of kaolin, 20 parts of light calcium carbonate, 15 parts of zinc stearate, 10 parts of polyvinyl alcohol, and 15 parts of a modified acrylic resin emulsion, was prepared. Using the apparatus shown in FIG. 1, after coating and drying in air knife coater so that an undercoat coating solution and a dry coating amount of 6 g / m 2 base paper of 50 g / m 2, dry coating and cast coating a coating liquid The composition was applied so as to have an amount of 3 g / m 2, and was cast-finished by a cast drum heated to 90 ° C. The surface of the light-weight cast-coated paper thus obtained was good without defects, and the maximum coating speed was 150 m / min. The air permeability of the undercoated base paper was 80 seconds. Example 2 The diatomaceous earth of the undercoat coating liquid of Example 1 was applied to three-dimensional needle-shaped calcium carbonate urchin-like particles (callite SA oil absorption 60: manufactured by Shiraishi Industry Co., Ltd.) with zinc stearate of the cast coating liquid. A lightweight cast-coated paper was obtained in the same manner as in Example 1 except that paraffin wax was used. The surface of the light-weight cast coated paper thus obtained was good without defects, and the maximum coating speed was 130 m / min.
The air permeability of the undercoated base paper was 200 seconds. Comparative Example 1 A lightweight cast-coated paper was prepared in the same manner as in Example 1 except that diatomaceous earth in the undercoat coating solution was changed to kaolin (Astrabright oil absorption 40: manufactured by Georgia Kaolin Co.). Drying of the coating solution was slow and the maximum coating speed was 90 m / min, and pinholes were conspicuous on the surface of the cast coat, resulting in poor surface properties. To improve surface properties, the dry coating amount of the cast coat layer should be 10
g / m 2 or more was required, and the maximum coating speed became 60 m / min or less. The air permeability of the undercoated base paper is 500
Seconds. Comparative Example 2 45 parts of kaolin (Astrabright oil absorption 40), 20 parts of heavy calcium carbonate (Escalon # 1500 oil absorption 28: manufactured by Sankyo Seiko Co., Ltd.), polyvinyl alcohol (Kosenol N-300 Nippon Synthetic Chemical Co., Ltd.) 15 parts, styrene-butadiene latex (JSR 0561, Japan Synthetic Rubber Co., Ltd.) 20
An undercoat coating liquid having a solid content concentration of 45% was prepared. Using this undercoat coating solution and the cast coating solution of Example 1, a lightweight cast-coated paper was produced in the same manner as in Example 1. At this time, the air permeability of the undercoated base paper is 1000 seconds or more, the drying of the cast coat coating solution is slow, and the maximum coating speed is 40 m / min. And the surface of the cast coat had remarkable defects and poor surface properties. Comparative Example 3 A light-weight cast-coated paper was produced in the same manner as in Example 1 except that zinc stearate in the cast coat coating liquid was removed. The maximum coating speed at this time is 150m
/ min, and defects such as pinholes and uneven coating were noticeable on the surface of the cast coat. In order to improve the cast coat surface, the dry coating amount of the cast coat layer was required to be 10 g / m 2 or more, and the maximum coating speed became 80 m / min or less.
【図面の簡単な説明】 第1図は実施例で使用したコーターの概略図である。[Brief description of the drawings] FIG. 1 is a schematic view of a coater used in the embodiment.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭55−76198(JP,A) 特開 昭49−118906(JP,A) 特開 昭57−117694(JP,A) 特開 昭62−95285(JP,A) 特開 昭54−23545(JP,A) 特開 昭62−173293(JP,A) ────────────────────────────────────────────────── ─── Continuation of front page (56) References JP-A-55-76198 (JP, A) JP-A-49-118906 (JP, A) JP-A-57-117694 (JP, A) JP-A-62-95285 (JP, A) JP-A-54-23545 (JP, A) JP-A-62-173293 (JP, A)
Claims (1)
量(JIS K5101)50m1/100g以上の顔料を10〜80重量%含
有するアンダーコート層を設けた、透気度(JIS P811
7)300秒以下の基紙上に、顔料、熱可融性物質及び結着
剤を主成分とするキャストコート層を設けることを特徴
とする軽量キャストコート紙の製造方法。 2.キャストコート層の塗布量が0.5〜10g/m2であるこ
とを特徴とする特許請求の範囲第1項記載の軽量キャス
トコート紙の製造方法。 3.キャストコート層の主成分が、顔料20〜60重量%、
熱可融性物質10〜50重量%、結着剤10〜40重量%である
ことを特徴とする特許請求の範囲第1項または第2項記
載の軽量キャストコート紙の製造方法。(57) [Claims] An undercoat layer containing a pigment and a binder as main components and containing 10 to 80% by weight of a pigment having an oil absorption (JIS K5101) of 50 m1 / 100 g or more is provided on a paper support.
7) A method for producing a lightweight cast-coated paper, comprising providing a cast coat layer containing pigment, a heat-fusible substance and a binder as main components on a base paper of 300 seconds or less. 2. 2. The method for producing a lightweight cast-coated paper according to claim 1, wherein the coating amount of the cast coat layer is 0.5 to 10 g / m < 2 >. 3. The main component of the cast coat layer is pigment 20 to 60% by weight,
3. The method for producing a lightweight cast-coated paper according to claim 1, wherein the content is 10 to 50% by weight of a heat-fusible substance and 10 to 40% by weight of a binder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62035795A JP2717177B2 (en) | 1987-02-20 | 1987-02-20 | Manufacturing method of lightweight cast coated paper |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62035795A JP2717177B2 (en) | 1987-02-20 | 1987-02-20 | Manufacturing method of lightweight cast coated paper |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63211394A JPS63211394A (en) | 1988-09-02 |
JP2717177B2 true JP2717177B2 (en) | 1998-02-18 |
Family
ID=12451856
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62035795A Expired - Fee Related JP2717177B2 (en) | 1987-02-20 | 1987-02-20 | Manufacturing method of lightweight cast coated paper |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2717177B2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0345800A (en) * | 1989-07-14 | 1991-02-27 | Nitto Denko Corp | Air-permeable laminated paper for screen printing |
JP3402514B2 (en) * | 1993-06-24 | 2003-05-06 | 三菱製紙株式会社 | Inkjet recording sheet |
AU2216797A (en) | 1996-03-26 | 1997-10-17 | International Group, Inc., The | Repulpable moisture resistant coated articles and methods of making and repulping the same |
JP4978404B2 (en) * | 2007-09-28 | 2012-07-18 | 大日本印刷株式会社 | Thermal transfer image receiving sheet |
JP5308223B2 (en) * | 2009-04-24 | 2013-10-09 | 大王製紙株式会社 | Coated paper |
FR3062660B1 (en) * | 2017-02-03 | 2019-06-07 | Ahlstrom-Munksjö Oyj | DECORATION PAPER FOR LAMINATES |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS575916B2 (en) * | 1973-03-24 | 1982-02-02 | ||
JPS5576198A (en) * | 1978-11-27 | 1980-06-09 | Kanzaki Paper Mfg Co Ltd | Production of casted coat paper |
-
1987
- 1987-02-20 JP JP62035795A patent/JP2717177B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPS63211394A (en) | 1988-09-02 |
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