JPH0122399B2 - - Google Patents

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Publication number
JPH0122399B2
JPH0122399B2 JP57140807A JP14080782A JPH0122399B2 JP H0122399 B2 JPH0122399 B2 JP H0122399B2 JP 57140807 A JP57140807 A JP 57140807A JP 14080782 A JP14080782 A JP 14080782A JP H0122399 B2 JPH0122399 B2 JP H0122399B2
Authority
JP
Japan
Prior art keywords
coating
coating liquid
paper
coated paper
coated
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
Application number
JP57140807A
Other languages
Japanese (ja)
Other versions
JPS5930992A (en
Inventor
Masato Nakamura
Teiji Kamioka
Noritoshi Watanabe
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kanzaki Paper Manufacturing Co Ltd
Original Assignee
Kanzaki Paper Manufacturing Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kanzaki Paper Manufacturing Co Ltd filed Critical Kanzaki Paper Manufacturing Co Ltd
Priority to JP14080782A priority Critical patent/JPS5930992A/en
Priority to DE19833328064 priority patent/DE3328064A1/en
Priority to FR8313285A priority patent/FR2531731B1/en
Publication of JPS5930992A publication Critical patent/JPS5930992A/en
Publication of JPH0122399B2 publication Critical patent/JPH0122399B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は塗被紙の製造方法に関するものであ
り、特定されたカオリンと重質炭酸カルシウムと
を顔料として含有する高固形分濃度の塗被液を、
特定の塗工方法によつて塗工することを特徴とす
る塗被加工紙の製造方法に関するものである。 顔料と接着剤とを含有する塗被液を、基紙に塗
布して乾燥することからなる塗被紙の製造法に於
て、63〜80wt%といつた高固形分濃度の塗被液
を塗工するブレードコーテイング法は、塗被液層
の乾燥速度が速いため、乾燥に要する設備、エネ
ルギー、経費を節減できるばかりでなく、塗被液
層が基紙の凹凸面に沿つて移動する以前に固化す
るため、優れた光沢度と平滑性を塗被紙に付与で
きる利点を備えている。 しかしながら、かかる高固形分濃度を有する塗
被液の塗工は、塗工に伴う種々の技術的問題点及
び得られる塗被紙の品質上の欠陥がいまだ解決さ
れておらず、工業的規模では殆ど実施されていな
いのが実情である。 例えば、63wt%以上、より好ましくは65wt%
以上の高固形分濃度塗被液を得るために、従来、
紙塗工に使われている塗被液の固形分濃度を単に
高めるだけでは粘度が高くなり、高剪断流動性も
悪く、保水性の低下した塗被液となつてしまう。
そのため塗工の際ストリーク、スタラクタイトな
どの条跡トラブルを引き起し易い。塗工適性を改
善するために比較的平均粒子径の大きな重質炭酸
カルシウムを顔料として併用する方法(特公昭46
−43244号)や、粒度分布を規制した微粒の重質
炭酸カルシウムを単独に顔料成分として用いる方
法(特開昭55−62296号)なども提案されている
が、いずれも塗工適性の改善に伴つて得られる塗
被紙の光沢度、平滑性が低下するという欠点が付
随する。 さらに、今日一般的に用いられているブレード
コータにおいては高固形分濃度塗被液の塗工に関
し上記の如き塗被液の塗工適性のみならず、次の
ような難点が付随する。即ち、フラデツドニツプ
タイプのロールアプリケート機構やフアウンテン
アプリケート機構を有するトレーリングブレード
方式にあつては、 塗工量が付き過ぎるため、ブレードの加圧機
構でのコントロールが難しく、しかも均一な塗
工量を得ることが至難である。 塗工量をコントロールするために、ブレード
圧力を強くすると塗工面ががさつき平滑性が悪
くなる。又紙切れが起り易く操業性も悪化す
る。 基紙に過剰の塗被液を供給した後、余剰の塗
被液を掻き落とすまでの時間が長い(例:ベロ
イト社フラデツドニツプコーターでコーター速
度1000m/分の場合0.024秒)ために、塗被液
層から基紙中への塗被液の浸透が進み、高濃度
であることも相俟つて脱水による塗被液層の保
水性の低下を来たし、塗被液層のゲル化、レベ
リング不良を引き起す。そのため塗工面が不均
一になるのみならず、ストリーク、スタラクタ
イトなどの条跡トラブルを起し易い。 またポンドタイプのパドルコーターではブレー
ドで掻き落とされた塗被液の自己クリーニング効
果が乏しいために、ストリーク、スタラクタイト
などが発生し易く、高固形分濃度塗被液の塗工に
は適しておらず、しかも紙切れ時などの操業性が
悪いという欠点がある。 かかる現状に鑑み、本発明者らは高固形分濃度
塗被液及び塗工方法において指摘される上記の如
き欠点を解消するべき鋭意研究の結果、特定され
た粒径を有するカオリンと重質炭酸カルシウムと
を顔料として併用することにより塗被液の塗工適
性を改善し、更にこれに基紙に過剰の塗被液を供
給して後、余剰の塗被液を掻き落とすまでの時間
を短くした特定の塗工方法を組み合せることによ
り高固形分濃度塗被液の塗工を可能とし、しかも
高品質の塗被加工紙を与え得る塗被紙の製造方法
を見い出したものである。 本発明は、顔料と接着剤を含有する高固形分濃
度の塗被液を基紙に塗被することにより塗被紙を
製造する方法に於て、(a)顔料として1μm以下の
粒子含有率が50wt%以上であるカオリンを全顔
料の10〜80wt%、2μm以下の粒子含有率が70〜
100wt%で、1μm以下の粒子含有率が55〜95wt%
である重質炭酸カルシウムを全顔料の20〜90wt
%含有し、かつ固形分濃度が63〜80wt%である
塗被液を、(b)ブレードコーターのアプリケート機
構で基紙に過剰に供給した後、0.0005〜0.015秒
の間にブレード機構で余剰の塗被液を掻き落とす
ことを特徴とする塗被紙の製造方法である。 本発明において用いられる塗被液に於て、その
顔料成分として使用されるカオリンは、主として
塗被紙の光沢度及び平滑性に寄与する成分であつ
て、これには1μm以下の粒子含有率が50wt%以
上であるカオリンが用いられる。カオリンの使用
量は全顔料の10〜80wt%の範囲であることを可
とし、10wt%未満では塗被紙に充分な光沢度と
平滑性を付与することができず、80wt%を越え
ると塗被液の塗工適性が悪化する。 上記のカオリンと共に顔料成分として使用され
る重質炭酸カルシウムは、主として塗被液の塗工
適性に寄与する成分である。しかし、前述の特公
昭46−43244号の如く、余り粗い重質炭酸カルシ
ウムを使用すると、塗工時にストリークやスクラ
ツチなどの条跡トラブルが発生しやすくなるばか
りではなく、白紙の光沢度、平滑性さらには印刷
後のインキ光沢も低下するため、本発明では2μ
m以下の粒子含有率が70〜100wt%、好ましくは
80〜100wt%であり、1μm以下の粒子含有率が55
〜95wt%、好ましくは60〜95wt%である微細な
重質炭酸カルシウムを使用する。重質炭酸カルシ
ウムの使用量は全顔料の20〜90wt%の範囲にあ
り、20wt%未満では塗被液の高剪断粘度が増大
して塗工時にトラブルが発生し、90wt%を越え
た場合は塗被紙の光択度及び平滑性が悪化し印刷
後のインキ光沢も低下する。 本発明で用いられる塗被液中の顔料成分は、主
として上記したカオリンと重質炭酸カルシウムで
構成されるが、必要に応じて他の顔料成分、例え
ば軽質炭酸カルシウム、サチンホワイト、二酸化
チタン、パイロフイライトクレー、亜硫酸カルシ
ウム、硫酸カルシウム、水酸化アルミニウム、酸
化亜鉛、タルク、ゼオライト、硫酸バリウム、無
定形シリカ、プララスチツクピグメトなどを配合
することもできる。しかし、それらの配合量は全
顔料の50wt%以下に抑えるべきであつて、一般
的には20wt%以下であるのが好ましい。 本発明で用いられる塗被液に於て、その接着剤
成分としては、スチレン−ブタジエン系、スチレ
ン−アクリル系、酢ビ−アクリル系、エチレン−
酢ビ系、ブタジエン−メチルメタクリル系、酢ビ
−ブチルアクリレート系等の各種共重合体および
ポリ酢酸ビニルなどのアルカリ感応性又はアルカ
リ非感応性接着剤、さらにはポリビニルアルコー
ル、無水マレイン酸−スチレン共重合体、イソブ
テン−無水マレイン酸共重合体、アクリル酸−メ
チルメタクリレート系共重合体などの合成系接着
剤、酸化澱粉、エーテル化澱粉、エステル化澱
粉、酸素変性澱粉やそれらをフラツシユドライし
て得られる冷水化溶性澱粉、カゼイン、大豆蛋白
などの天然系接着剤など一般に知られた接着剤を
用いることが出来るが、63wt%以上の高固形分
濃度で、かつレオロジー特性の良好な塗被液を得
るためには、上記共重合体のラテツクス単独、若
しくはこれに冷水可溶性澱粉を併用するのが好ま
しく、接着剤の総使用量も対顔料3〜20wt%の
範囲内に留めるのが望ましい。そして、他の天然
系接着剤など増粘傾向の強い接着剤の使用は最小
量とするのが好ましい。なお、必要に応じて分散
剤、増粘剤、保水剤、消泡剤、耐水化剤、滑剤、
染料、PH調節剤など各種の助剤を適宜配合するこ
とができる。 かくして得られる塗被液は、特定のカオリンと
重質炭酸カルシウムとを顔料として併用すること
により、固形分濃度63〜80wt%好ましくは65〜
80wt%に調整でき、しかも、低粘度で高剪断流
動性も良好なブレードコーター塗工適性に優れた
ものとなる。 本発明の方法に於ては、かかる特定の高固形分
濃度塗被液を特定の塗工方法と組み合せるもので
あるが、かかる特定の塗工方法とは、ブレードコ
ーターに於て基紙に目的とする塗工量の15〜30
倍、好ましくは10〜20倍程度の過剰の塗被液を供
給して後、余剰の塗被液を掻き落とすまでの時間
を0.0005〜0.015秒、より好ましくは0.001〜0.01
秒と極めて短くした塗工方法のことである。一般
に、かかる塗工方法は塗被液を基紙へ転移させる
アプリケート機構から、余剰の塗被液を掻き落と
すブレード機構までの距離を0.5〜16cm程度の範
囲、好ましくは0.5〜12cm、最も好ましくは0.5〜
7cmの範囲に調節することにより達成される。な
お、高固形分濃度塗被液を0.015秒以上経過後に
ブレードで掻き落とした場合にはストリーク、ス
タラクタイトなどの条跡トラブルが発生し易くな
つてしまう。また、0.0005秒よりも短い条件とは
コーター速度が3000m/分以上を意味するもので
あり、現状では安定操業が難しい。なお、本発明
の方法を適用して好ましい効果の得られるコータ
ー速度は、100〜2000m/分、より好ましくは100
〜1500m/分程度であ。 本発明において好ましく用いることのできる塗
工方法の一種が特開昭57−84770号に記載されて
いるが、そこでは全て固形分濃度が60wt%以下
の塗被液が用いられており、比較的軽量のコーテ
イングに関する技術が開示されているにすぎな
い。しかしながら本発明の方法では、当該塗工方
法に前述の如き優れたレオロジー特性を有する特
定の塗被液を組合せるものであり、かくすること
により63wt%以上、好ましくは65〜80wt%とい
つた高固形分濃度の塗被液をベベル型、ベント型
など任意のブレードにより、低いブレード圧で基
紙の片面あるいは両面に安定して塗工可能ならし
めるものである。しかも片面あたりの塗工量も乾
燥重量で3〜30g/m2といつた広範囲での調節が
可能となる。しかし塗工量が6g/m2未満では得
られる塗被紙の光沢度、平滑性、印刷後のインキ
光沢が不充分となり、逆に30g/m2を越えるとス
トリーク、スクラツチなどの条跡トラブルが起り
易くなるので本発明においては塗工量を6〜30
g/m2、好ましくは8〜20g/m2の範囲に留める
のが望ましく、またシングルコートのみならずダ
ブルコートも当然可能である。なお、基紙として
は一般に高歩留パルプ又はメカニカルパルプを用
いて酸性又は中性で抄紙された中質コート用原紙
や漂白パルプを用いた上質コート用原紙が用いら
れる。 かくして本発明の方法によれば、従来の高固形
分濃度塗被液塗工で認められた技術的問題点が効
果的に改善され、塗被液の選択吸収や塗工量ムラ
が少なく、塗工量のプロフアイル調節も容易とな
り、均一な塗被層が形成され、高固形分濃度塗被
液の塗工により期待される塗被加工紙特性、即ち
白紙の光沢度、平滑性、印刷後のインキ光沢など
が著しく改良されるものである。 さらに、本発明の方法によれば従来要求されて
いた塗被液の保水性もさほど必要とはされず、基
紙へ塗被された後の塗被液層の保水性の低下を最
小限に保つことができ、流動性が失われずに、し
かも低いブレード圧力で塗工できるために、スト
リーク、スタラクタイト、スクラツチなどの条跡
トラブルや、紙切れが少なくなり、塗工操業性も
著しく改良されるものである。勿論、高固形分濃
度塗工により達せられる乾燥設備、エネルギー経
費の節減は当然の効果として得られるものであ
る。 本発明の方法により得られる塗被紙は、スーパ
ーキヤレンダー、グロスキヤレンダーなどの仕上
げ装置を経て製品化された場合に本発明の優れた
特性が顕著に発揮されるが、軽い仕上げ処理又は
仕上げ処理なしにマツト調の塗被加工紙としても
使用できる。そして塗被紙に対する印刷方式はオ
フセツト印刷、グラビア印刷、活版印刷、フレキ
ソ印刷の何れもが採用可能であり、枚葉又は巻取
りの何れでも使用可能である。 以下に実施例を挙げて本発明を更に具体的に説
明するが、本発明はこれらの実施例によつて限定
されるものではない。尚実施例において示す部お
よび%は特に記載のない限り重量部及び重量%を
意味する。 実施例1〜8、比較例4〜8 NBKP20部及びLBKP80部から成るパルプ組
成にロジンサイズ0.3部、抄紙用タルク15部を添
加し、硫酸バンドで抄紙PH4.5に調整して、長網
抄紙機にて抄紙し、酸化変成澱粉を両面で1.5
g/m2付着するようにサイズプレス処理を行い、
米坪55g/m2の塗被加工紙用原紙を得た。 コーレス分散機にて、表に記載した如き顔料、
接着剤及び助剤から成る塗被液組成に、分散剤と
してポリアクリル酸ソーダ0.2部、滑剤としてス
テアリン酸カルシウム0.3部を加えて混合分散し、
表に記載した如き性質の塗被液を調整した。 これらの塗被液は、上記原紙に、シヨートドウ
エルブレードコーターにて実施例1〜7、比較例
4〜8は片面で15g/m2、両面で30g/m2、また
実施例8は片面で8g/m2、両面で16g/m2とな
るように両面塗工された。この時実施例2のコー
ター速度は300m/分、実施例1、3、5〜8、
比較例4〜8のコーター速度は900m/分、また
実施例4のコーター速度は1400m/分で塗工さ
れ、その各々の塗被液を基紙に塗布し、ブレード
で掻き落とすまでの時間(表中にはドウエルタイ
ムと記載)は表に記載した如くであつた。 得られた塗被紙はスーパーキヤレンダー掛けを
行い、塗被加工紙を製造した。塗工操作性、塗被
加工紙の白紙及び印刷後品質は表に記載した如く
であつた。 比較例 1〜3 実施例1〜8、比較例4〜8と同じ原紙、及び
同様の塗料調整法により表に記載した如き性質の
塗被液を得た。 次にフラデツドニツプブレードコーターにて片
面で15g/m2、両面で30g/m2となるように両面
塗工され、その後スーパーキヤレンダー掛けを行
い塗被加工紙を製造した。 この時、比較例1のコーター速度は300m/分、
また比較例2、3のコーター速度は900m/分で
塗工され、その各々のドウエルタイムは表に記載
した如くであつた。 塗工操業性、塗被加工紙の白紙及び印刷後の品
質は表に記載した如くであつた。 実施例9、比較例9 SGP50部及びNBKP50部から成パルプ組成に、
ロジンサイズ0.2部、抄紙用タルク20部を添加し、
硫酸バンドで抄紙PH4.5に調整して長網抄紙機に
て抄紙し、米坪40g/m2の塗被加工紙用原紙を得
た。 次に実施例1〜8、比較例1〜8と同様の塗料
調整法により表に記載した如き性質の塗被液を得
た。 これらの塗被液は、上記原紙に、シヨートドウ
エルブレードコーターにて片面で15g/m2、両面
で30g/m2となるように両面塗工され、スーパー
キヤレンダー掛けを行い、塗被加工紙を製造し
た。 この時のコーター速度は900m/分で塗工され、
ドウエルタイムは表に記載した如きであつた。 塗工操業性、塗被加工紙の白紙及びグラビア印
刷後品質は表に記載した如くであつた。 以上の実施例により明らかなように、本発明の
塗被紙の製造方法は、高固形分濃度塗工の利点を
充分に発揮させるべく改良されており、塗被液の
レオロジー特性、塗工操業性に優れ、得られた塗
被加工紙の品質はいずれも白紙光沢度、平滑性に
優れ、またオフセツト印刷、グラビア印刷後の品
質にも優れた印刷用塗被加工紙であつた。
The present invention relates to a method for producing coated paper, in which a coating liquid with a high solid content concentration containing specified kaolin and heavy calcium carbonate as pigments,
The present invention relates to a method for producing coated paper, which is characterized by coating by a specific coating method. In the method of manufacturing coated paper, which involves applying a coating liquid containing pigments and adhesives onto a base paper and drying it, a coating liquid with a high solid content concentration of 63 to 80 wt% is used. The blade coating method allows the coating liquid layer to dry quickly, which not only saves equipment, energy, and expenses required for drying, but also allows the coating liquid layer to dry quickly before moving along the uneven surface of the base paper. It has the advantage of imparting excellent gloss and smoothness to coated paper. However, various technical problems associated with coating and defects in the quality of the resulting coated paper have not yet been solved, and coating solutions with such high solids concentrations have not been applied on an industrial scale. The reality is that it is almost never implemented. For example, 63wt% or more, more preferably 65wt%
In order to obtain a coating liquid with a high solid content concentration, conventionally,
Simply increasing the solid content concentration of a coating liquid used for paper coating will result in a coating liquid with increased viscosity, poor high shear fluidity, and reduced water retention.
Therefore, it is easy to cause streak problems such as streaks and stalactite during coating. A method of using heavy calcium carbonate, which has a relatively large average particle size, as a pigment in order to improve coating suitability.
-43244) and a method in which fine grained heavy calcium carbonate with a controlled particle size distribution is used solely as a pigment component (Japanese Unexamined Patent Publication No. 1983-62296), but none of these methods improve coating suitability. An accompanying drawback is that the gloss and smoothness of the coated paper obtained are reduced. Furthermore, in the blade coater commonly used today, in addition to the above-mentioned suitability for coating a coating liquid with a high solid content concentration, the following problems are also involved. In other words, in the case of a trailing blade method that has a flattened nip type roll applicator mechanism or a fountain applicator mechanism, the coating amount is too large, making it difficult to control with the blade's pressure mechanism, and moreover, it is difficult to control the coating uniformly. It is extremely difficult to obtain a sufficient coating amount. If the blade pressure is increased to control the coating amount, the coated surface will become rough and the smoothness will deteriorate. In addition, paper breaks easily occur, and operability deteriorates. After supplying excess coating liquid to the base paper, it takes a long time to scrape off the excess coating liquid (e.g., 0.024 seconds when using a Beloit Co., Ltd. Fradetsu nip coater at a coater speed of 1000 m/min). The penetration of the coating liquid from the coating liquid layer into the base paper progresses, and combined with the high concentration, the water retention capacity of the coating liquid layer decreases due to dehydration, resulting in gelation and leveling of the coating liquid layer. cause defects. This not only makes the coated surface non-uniform, but also tends to cause streak troubles such as streaks and stalactite. In addition, pound-type paddle coaters have a poor self-cleaning effect on the coating liquid scraped off by the blade, so streaks and stalactite are likely to occur, making them unsuitable for coating high solids concentration coating liquids. Moreover, it has the disadvantage of poor operability when running out of paper. In view of the current situation, the present inventors conducted extensive research to eliminate the above-mentioned drawbacks pointed out in high solids concentration coating liquids and coating methods, and as a result, the present inventors developed kaolin and heavy carbonate having a specified particle size. By using calcium as a pigment, the coating suitability of the coating liquid is improved, and the time required to scrape off the excess coating liquid after supplying excess coating liquid to the base paper is shortened. By combining the specific coating methods described above, we have discovered a method for producing coated paper that enables the coating of a coating liquid with a high solid content concentration and that also provides coated paper of high quality. The present invention provides a method for producing coated paper by coating a base paper with a coating liquid containing a pigment and an adhesive and having a high solid content concentration. Kaolin with a content of 50wt% or more is 10-80wt% of the total pigment, and the particle content of 2 μm or less is 70-80wt% of the total pigment.
100wt%, particle content of 1μm or less is 55-95wt%
20~90wt of total pigment is heavy calcium carbonate
% and has a solid content concentration of 63 to 80 wt%, is supplied to the base paper in excess by the application mechanism of the (b) blade coater, and then the excess is removed by the blade mechanism within 0.0005 to 0.015 seconds. This is a method for producing coated paper characterized by scraping off the coating liquid. Kaolin, which is used as a pigment component in the coating liquid used in the present invention, is a component that mainly contributes to the gloss and smoothness of the coated paper, and it contains particles with a particle content of 1 μm or less. Kaolin with a content of 50 wt% or more is used. The amount of kaolin used can range from 10 to 80 wt% of the total pigment. If it is less than 10 wt%, it will not be possible to impart sufficient gloss and smoothness to the coated paper, and if it exceeds 80 wt%, it will not be possible to impart sufficient gloss and smoothness to the coated paper. The coating suitability of the liquid to be applied deteriorates. Heavy calcium carbonate, which is used as a pigment component together with the above-mentioned kaolin, is a component that mainly contributes to the coating suitability of the coating liquid. However, as in the above-mentioned Japanese Patent Publication No. 46-43244, using too coarse heavy calcium carbonate not only tends to cause problems with streaks and scratches during coating, but also reduces the gloss and smoothness of the white paper. Furthermore, since the ink gloss after printing also decreases, the present invention uses 2μ
Particle content below m is 70-100wt%, preferably
80-100wt%, and the particle content of 1μm or less is 55
~95 wt%, preferably 60-95 wt% of finely ground calcium carbonate is used. The amount of heavy calcium carbonate used is in the range of 20 to 90 wt% of the total pigment. If it is less than 20 wt%, the high shear viscosity of the coating liquid will increase and trouble will occur during coating, and if it exceeds 90 wt%, The photoselectivity and smoothness of the coated paper deteriorate, and the gloss of the ink after printing also decreases. The pigment components in the coating liquid used in the present invention are mainly composed of the above-mentioned kaolin and heavy calcium carbonate, but other pigment components may be added as necessary, such as light calcium carbonate, satin white, titanium dioxide, and pyrocarbonate. Fiberite clay, calcium sulfite, calcium sulfate, aluminum hydroxide, zinc oxide, talc, zeolite, barium sulfate, amorphous silica, plastic pigment, and the like can also be blended. However, their blending amount should be limited to 50 wt% or less of the total pigments, and is generally preferably 20 wt% or less. In the coating liquid used in the present invention, adhesive components include styrene-butadiene, styrene-acrylic, vinyl acetate-acrylic, and ethylene-butadiene.
Various copolymers such as vinyl acetate, butadiene-methyl methacrylate, and vinyl acetate-butyl acrylate, and alkali-sensitive or alkali-insensitive adhesives such as polyvinyl acetate, as well as polyvinyl alcohol, maleic anhydride-styrene, etc. Synthetic adhesives such as polymers, isobutene-maleic anhydride copolymers, acrylic acid-methyl methacrylate copolymers, oxidized starches, etherified starches, esterified starches, oxygen-modified starches, and flat-dried them. Generally known adhesives such as natural adhesives such as cold-water soluble starch, casein, and soybean protein can be used, but coating liquids with a high solids concentration of 63 wt% or more and good rheological properties can be used. In order to obtain this, it is preferable to use the copolymer latex alone or in combination with cold water-soluble starch, and it is desirable to keep the total amount of adhesive used within the range of 3 to 20 wt% based on the pigment. It is also preferable to minimize the amount of adhesives that tend to thicken, such as other natural adhesives. In addition, dispersants, thickeners, water retention agents, antifoaming agents, waterproofing agents, lubricants,
Various auxiliary agents such as dyes and PH regulators can be added as appropriate. The coating liquid obtained in this way has a solid content concentration of 63 to 80 wt%, preferably 65 to 80%, by using a specific kaolin and heavy calcium carbonate as pigments.
It can be adjusted to 80wt%, and has low viscosity and good high shear fluidity, making it highly suitable for application with a blade coater. In the method of the present invention, such a specific coating liquid with a high solid content concentration is combined with a specific coating method, and this specific coating method is a combination of coating liquid with a high solids concentration and a specific coating method. 15-30 of the desired coating amount
After supplying excess coating liquid, preferably about 10 to 20 times, the time required to scrape off the excess coating liquid is 0.0005 to 0.015 seconds, more preferably 0.001 to 0.01 seconds.
This is a coating method that is extremely short, taking just seconds. In general, such a coating method requires that the distance from the applicator mechanism that transfers the coating liquid to the base paper to the blade mechanism that scrapes off excess coating liquid range from about 0.5 to 16 cm, preferably from 0.5 to 12 cm, and most preferably from about 0.5 to 12 cm. is 0.5~
This is achieved by adjusting the range to 7 cm. Note that if a high solids concentration coating liquid is scraped off with a blade after 0.015 seconds or more has elapsed, streak problems such as streaks and stalactite are likely to occur. Furthermore, the condition shorter than 0.0005 seconds means that the coater speed is 3000 m/min or more, and stable operation is currently difficult. The coater speed at which a preferable effect can be obtained by applying the method of the present invention is 100 to 2000 m/min, more preferably 100 m/min.
~1500m/min. One type of coating method that can be preferably used in the present invention is described in JP-A-57-84770, in which coating liquids with a solid content concentration of 60 wt% or less are used, which is relatively Only techniques relating to lightweight coatings are disclosed. However, in the method of the present invention, a specific coating liquid having excellent rheological properties as described above is combined with the coating method, thereby achieving a concentration of 63 wt% or more, preferably 65 to 80 wt%. It is possible to stably coat one or both sides of a base paper with a low blade pressure using any blade such as a bevel type or bent type with a coating liquid having a high solid content concentration. Furthermore, the amount of coating per side can be adjusted over a wide range of 3 to 30 g/m 2 in terms of dry weight. However, if the coating amount is less than 6g/ m2 , the resulting coated paper will have insufficient gloss, smoothness, and ink gloss after printing, while if it exceeds 30g/ m2 , streaks such as streaks and scratches will occur. In the present invention, the coating amount is set at 6 to 30%.
g/m 2 , preferably within the range of 8 to 20 g/m 2 , and not only single coating but also double coating is of course possible. In addition, as the base paper, generally used is a medium-quality base paper for coating made using acidic or neutral paper using high-yield pulp or mechanical pulp, or high-quality base paper for coating using bleached pulp. Thus, according to the method of the present invention, the technical problems observed in the conventional high solids concentration coating liquid coating are effectively improved, and selective absorption of the coating liquid and coating amount unevenness are reduced, and coating is possible. It is easier to adjust the profile of the work load, a uniform coating layer is formed, and the coated paper properties expected by coating with a high solids concentration coating liquid, such as white paper gloss, smoothness, and after printing, are improved. The gloss of the ink is significantly improved. Furthermore, according to the method of the present invention, the water retention property of the coating liquid, which was conventionally required, is not required so much, and the decrease in the water retention property of the coating liquid layer after being coated on the base paper is minimized. Because coating can be performed with low blade pressure without loss of fluidity, streak problems such as streaks, stalactite, and scratches, as well as paper breakage, are reduced, and coating operability is significantly improved. It is something. Of course, the savings in drying equipment and energy costs that can be achieved by coating with a high solid content concentration are a natural effect. The coated paper obtained by the method of the present invention exhibits the excellent characteristics of the present invention significantly when it is made into a product through finishing equipment such as a super calender or a gloss calender. It can also be used as coated matte paper without treatment. Any of offset printing, gravure printing, letterpress printing, and flexo printing can be used as the printing method for coated paper, and either sheet or roll printing can be used. The present invention will be described in more detail below with reference to Examples, but the present invention is not limited to these Examples. Note that parts and percentages shown in the examples mean parts by weight and percentages by weight unless otherwise specified. Examples 1 to 8, Comparative Examples 4 to 8 0.3 parts of rosin size and 15 parts of papermaking talc were added to the pulp composition consisting of 20 parts of NBKP and 80 parts of LBKP, and the papermaking pH was adjusted to 4.5 with sulfuric acid band to make fourdrinier paper. Paper is made using a machine, and oxidized modified starch is added to 1.5% on both sides.
Perform size press treatment to adhere to g/ m2 ,
A base paper for coated paper having a weight of 55 g/m 2 was obtained. Using a Coles disperser, pigments as listed in the table,
Add 0.2 parts of sodium polyacrylate as a dispersant and 0.3 parts of calcium stearate as a lubricant to a coating liquid composition consisting of an adhesive and an auxiliary agent, mix and disperse,
A coating solution was prepared with the properties listed in the table. These coating liquids were applied to the above base paper using a short dwell blade coater in Examples 1 to 7, Comparative Examples 4 to 8 at 15 g/m 2 on one side, 30 g/m 2 on both sides, and Example 8 on one side. Both sides were coated so that the weight was 8 g/m 2 and the weight was 16 g/m 2 on both sides. At this time, the coater speed of Example 2 was 300 m/min, Examples 1, 3, 5 to 8,
The coater speed of Comparative Examples 4 to 8 was 900 m/min, and the coater speed of Example 4 was 1400 m/min. The dwell time (described as dwell time in the table) was as described in the table. The obtained coated paper was subjected to super calendering to produce coated processed paper. The coating operability, the blank paper of the coated paper and the quality after printing were as shown in the table. Comparative Examples 1 to 3 Using the same base paper and the same coating preparation method as in Examples 1 to 8 and Comparative Examples 4 to 8, coating liquids having properties as described in the table were obtained. Next, the paper was coated on both sides using a flattened nip blade coater at a coating weight of 15 g/m 2 on one side and 30 g/m 2 on both sides, and then subjected to super calendering to produce a coated paper. At this time, the coater speed of Comparative Example 1 was 300 m/min.
Further, the coater speed of Comparative Examples 2 and 3 was 900 m/min, and the respective dwell times were as shown in the table. The coating operability, the quality of the coated paper and the quality after printing were as shown in the table. Example 9, Comparative Example 9 Pulp composition from 50 parts of SGP and 50 parts of NBKP,
Add 0.2 parts of rosin size and 20 parts of talc for paper making,
The pH of the paper was adjusted to 4.5 using sulfuric acid band, and paper was made using a Fourdrinier paper machine to obtain base paper for coated processed paper with a weight of 40 g/m 2 . Next, coating liquids having the properties shown in the table were obtained by the same coating preparation method as in Examples 1 to 8 and Comparative Examples 1 to 8. These coating liquids were coated on both sides of the above base paper using a short dwell blade coater at a coating density of 15 g/m 2 on one side and 30 g/m 2 on both sides, followed by super calendering and coating processing. produced paper. The coater speed at this time was 900 m/min.
Dwell time was as listed in the table. The coating operability, the white paper of the coated paper and the quality after gravure printing were as shown in the table. As is clear from the above examples, the method for producing coated paper of the present invention has been improved to fully utilize the advantages of high solids concentration coating, and the rheological properties of the coating liquid and the coating operation The obtained coated processed paper was excellent in white paper gloss and smoothness, and was also excellent in quality after offset printing and gravure printing.

【表】【table】

【表】 実施例、比較例で使用した塗被液原料の説明 実施例1〜5、7、8、比較例1〜5、7で使
用したカオリンは商品名アマゾン88(The
Caulim da Amazonia Ltda.社製)。 実施例6で使用したカオリンは商品名HT
(EMC社製)。 実施例9、比較例9で使用したカオリンは商品
名ウルトラホワイト90(EMC社製)。 比較例6で使用したカオリンは商品名
Klondyke(EMC社製)。 実施例1〜6、8、9、比較例1〜6、8、9
で使用した重質炭酸カルシウムは商品名カービタ
ル90(富士カオリン社製)。 実施例7で使用した重質炭酸カルシウムは、商
品名ソフトン1800(備北粉化工業社製)を、分散
剤としてポリアクリル酸ソーダを対顔料0.4部用
いてスラリー化した後、西独ドライスベルケ社製
サンドミル(パールミル)にて微粉砕し製造し
た。 比較例7で使用した重質炭酸カルシウムは商品
名ソフトン1800。 実施例1〜8、比較例1〜8で使用したラテツ
クスAはスチレン−ブタジエン共重合ラテツクス
商品名SN307(住友ノーガタツク社製)。 実施例9、比較例9で使用したラテツクスBは
アルカリ増粘型スチレン−ブタジエン−ブチルア
クリレート−メチルメタアクリレート共重合ラテ
ツクス商品名L−1953(旭ダウ社製)。 実施例1〜4、6〜8、比較例1〜3、6〜8
で使用した澱粉Aは商品名ハイコースターPC11
(三和澱粉社製)。 比較例4で使用した澱粉Bは商品名エースA
(王子コーンスターチ社製)。 表中の注 注1 粒度分布:セデイグラフ5000−01型(島
津製作所製)により測定し、百分率(%)で
示す。 注2 B型粘度:ブルツクフイールド型粘度計
のNo.1スピドル60rpmに於ける粘度値をセン
チポイズ(cps)で示す。 注3 高剪断粘度:ハーキユレス高剪断粘度計
(熊谷理機工業製)によりBob E、
8000rpm、即ち8.4×104sec-1に於ける粘度値
をポイズ(cps)で示す。 注4 塗工操業性:ストリーク、スクラツチ、
スタラクタイトの条跡欠陥及び塗工面の均一
性により評価した。 (良好◎ 〇 △ ×(操作不可) 注5 白紙光沢度:材上式光沢度計により
75゜/75゜に於ける測定値を%で示す。 注6 白紙平滑性:目視にて評価した。 (良好)◎ 〇 △ ×(劣る) 注7 印刷光沢度:明製作所製RI型印刷試験
機を使用し墨インキ0.3c.c.にて印刷後注5と
同様に光沢度の測定値を%で示す。 注8 グラビア適性:熊谷理機工業製 グラビア印刷試験機により印刷後網点再現
性を目視にて評価した。 (良好)◎ 〇 △ ×(劣る)
[Table] Description of coating liquid raw materials used in Examples and Comparative Examples The kaolin used in Examples 1 to 5, 7, and 8 and Comparative Examples 1 to 5, and 7 was manufactured under the trade name Amazon 88 (The
Caulim da Amazonia Ltda.). The kaolin used in Example 6 has the trade name HT.
(Manufactured by EMC). The kaolin used in Example 9 and Comparative Example 9 was under the trade name Ultra White 90 (manufactured by EMC). The kaolin used in Comparative Example 6 is the trade name
Klondyke (manufactured by EMC). Examples 1-6, 8, 9, Comparative Examples 1-6, 8, 9
The heavy calcium carbonate used was the product name Carbital 90 (manufactured by Fuji Kaolin Co., Ltd.). The heavy calcium carbonate used in Example 7 was obtained by slurrying the product name Softon 1800 (manufactured by Bihoku Funka Kogyo Co., Ltd.) using 0.4 parts of sodium polyacrylate as a dispersant, and then milling it in a sand mill manufactured by Dreiswerke, Germany. (Pearl Mill). The heavy calcium carbonate used in Comparative Example 7 had the trade name Softon 1800. Latex A used in Examples 1 to 8 and Comparative Examples 1 to 8 was a styrene-butadiene copolymer latex brand name SN307 (manufactured by Sumitomo Naugatak Co., Ltd.). The latex B used in Example 9 and Comparative Example 9 was an alkali-thickened styrene-butadiene-butyl acrylate-methyl methacrylate copolymer latex trade name L-1953 (manufactured by Asahi Dow Co., Ltd.). Examples 1-4, 6-8, Comparative Examples 1-3, 6-8
The starch A used in is the product name Hi-Coaster PC11.
(manufactured by Sanwa Starch Co., Ltd.). Starch B used in Comparative Example 4 has the trade name Ace A.
(manufactured by Oji Cornstarch Company). Notes in the table Note 1 Particle size distribution: Measured using Sedaygraph Model 5000-01 (manufactured by Shimadzu Corporation) and expressed in percentage (%). Note 2 Type B viscosity: The viscosity value measured at 60 rpm on the No. 1 spindle of a Bruckfield viscometer in centipoise (cps). Note 3 High shear viscosity: Bob E, determined by Hercules high shear viscometer (manufactured by Kumagai Riki Kogyo)
The viscosity value at 8000 rpm, that is, 8.4×10 4 sec -1 is expressed in poise (cps). Note 4 Coating operability: streaks, scratches,
The evaluation was based on the streak defects of stalactite and the uniformity of the coated surface. (Good ◎ 〇 △ × (unoperable) Note 5 White paper gloss: measured by on-board gloss meter
The measured value at 75°/75° is shown in %. Note 6 Blank paper smoothness: Visually evaluated. (Good) ◎ 〇 △ × (Poor) Note 7 Print gloss: After printing with 0.3 cc of black ink using an RI type printing tester manufactured by Mei Seisakusho, the measured value of gloss is shown in % as in Note 5. Note 8 Gravure suitability: Halftone dot reproducibility after printing was visually evaluated using a gravure printing tester manufactured by Kumagai Riki Kogyo. (Good) ◎ 〇 △ × (Poor)

Claims (1)

【特許請求の範囲】[Claims] 1 顔料と接着剤を含有する高固形分濃度の塗被
液を基紙に塗被することにより塗被紙を製造する
方法に於て、(a)顔料として1μm以下の粒子含有
率が50w%以上であるカオリンを全顔料の10〜
80w%、2μm以下の粒子含有率が70〜100w%で、
1μm以下の粒子含有率が55〜95w%である重質炭
酸カルシウムを全顔料の20〜90w%含有し、かつ
固形分濃度が63〜80w%である塗被液を、(b)ブレ
ードコーターのアプリケート機構で基紙に過剰に
供給した後、0.0005〜0.015秒の間にブレード機
構で余剰の塗被液を掻き落とすことを特徴とする
塗被紙の製造方法。
1. In a method of manufacturing coated paper by coating a base paper with a high solids concentration coating liquid containing pigments and adhesives, (a) the content of particles of 1 μm or less as pigments is 50w%; Kaolin is more than 10% of the total pigment
80w%, particle content of 2μm or less is 70-100w%,
A coating liquid containing 20 to 90 w% of the total pigment, with a particle content of 55 to 95 w% of particles of 1 μm or less, and a solid content concentration of 63 to 80 w%, is applied to (b) a blade coater. A method for producing coated paper, which comprises supplying excess coating liquid to the base paper using an applicator mechanism and then scraping off excess coating liquid using a blade mechanism within 0.0005 to 0.015 seconds.
JP14080782A 1982-08-12 1982-08-12 Production of coated paper Granted JPS5930992A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP14080782A JPS5930992A (en) 1982-08-12 1982-08-12 Production of coated paper
DE19833328064 DE3328064A1 (en) 1982-08-12 1983-08-03 Process for the manufacture of coated paper
FR8313285A FR2531731B1 (en) 1982-08-12 1983-08-12 PROCESS FOR PRODUCING PAPER COATED WITH A COATING, PARTICULARLY FOR PRINTING

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14080782A JPS5930992A (en) 1982-08-12 1982-08-12 Production of coated paper

Publications (2)

Publication Number Publication Date
JPS5930992A JPS5930992A (en) 1984-02-18
JPH0122399B2 true JPH0122399B2 (en) 1989-04-26

Family

ID=15277189

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14080782A Granted JPS5930992A (en) 1982-08-12 1982-08-12 Production of coated paper

Country Status (1)

Country Link
JP (1) JPS5930992A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006152528A (en) * 2004-10-26 2006-06-15 Oji Paper Co Ltd Pigment-coated paper

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0692724B2 (en) * 1984-09-28 1994-11-16 株式会社日立製作所 Reactor isolation cooling system
JPS61252393A (en) * 1985-04-26 1986-11-10 本州製紙株式会社 Coating composition for flexographic printing paper
WO2004030917A1 (en) * 2002-10-01 2004-04-15 Sappi Netherlands Services B.V. Coated printing sheet and process for making same
JP5328454B2 (en) * 2009-03-31 2013-10-30 日本製紙株式会社 Gravure / offset rotary printing paper

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55142794A (en) * 1979-04-17 1980-11-07 Kanzaki Paper Mfg Co Ltd Production of medium quality coated paper for offfwheel
JPS55152895A (en) * 1979-05-11 1980-11-28 Kanzaki Paper Mfg Co Ltd Production of medium grade coat paper for graphic wheel
JPS56159395A (en) * 1980-05-14 1981-12-08 Sanyo Kokusaku Pulp Co Production of pigment coated paper
JPS5766196A (en) * 1980-10-11 1982-04-22 Kanzaki Paper Mfg Co Ltd Production of medium quality coated paper for offset
JPS5766195A (en) * 1980-10-03 1982-04-22 Oji Paper Co Coating liquid composition
JPS5784770A (en) * 1980-11-04 1982-05-27 Cons Paper Inc Method of adding coating liquid to moving paper web and applicator for said method

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55142794A (en) * 1979-04-17 1980-11-07 Kanzaki Paper Mfg Co Ltd Production of medium quality coated paper for offfwheel
JPS55152895A (en) * 1979-05-11 1980-11-28 Kanzaki Paper Mfg Co Ltd Production of medium grade coat paper for graphic wheel
JPS56159395A (en) * 1980-05-14 1981-12-08 Sanyo Kokusaku Pulp Co Production of pigment coated paper
JPS5766195A (en) * 1980-10-03 1982-04-22 Oji Paper Co Coating liquid composition
JPS5766196A (en) * 1980-10-11 1982-04-22 Kanzaki Paper Mfg Co Ltd Production of medium quality coated paper for offset
JPS5784770A (en) * 1980-11-04 1982-05-27 Cons Paper Inc Method of adding coating liquid to moving paper web and applicator for said method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006152528A (en) * 2004-10-26 2006-06-15 Oji Paper Co Ltd Pigment-coated paper

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Publication number Publication date
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