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JPS6410638B2 - - Google Patents
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JPS6410638B2 - - Google Patents

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Publication number
JPS6410638B2
JPS6410638B2 JP715880A JP715880A JPS6410638B2 JP S6410638 B2 JPS6410638 B2 JP S6410638B2 JP 715880 A JP715880 A JP 715880A JP 715880 A JP715880 A JP 715880A JP S6410638 B2 JPS6410638 B2 JP S6410638B2
Authority
JP
Japan
Prior art keywords
paper
gloss
coating
parts
coated paper
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP715880A
Other languages
Japanese (ja)
Other versions
JPS56107098A (en
Inventor
Toshinobu Ogura
Masafumi Masuda
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.)
Mitsubishi Paper Mills Ltd
Original Assignee
Mitsubishi Paper Mills 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 Mitsubishi Paper Mills Ltd filed Critical Mitsubishi Paper Mills Ltd
Priority to JP715880A priority Critical patent/JPS56107098A/en
Priority to US06/203,223 priority patent/US4317849A/en
Publication of JPS56107098A publication Critical patent/JPS56107098A/en
Publication of JPS6410638B2 publication Critical patent/JPS6410638B2/ja
Granted legal-status Critical Current

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Description

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

本発明は優れた印刷適性を有する強光沢塗被紙
を安定かつ生産性良く提供しうる製造方法に関す
るものである。従来、強光沢紙の製造方法として
は、(1)湿潤塗被層を平滑な加熱仕上げ表面に圧接
して乾燥するウエツトキヤスト法(例えば特公昭
38−25160号)(2)湿潤塗被層を一旦乾燥した後、
再湿潤により塗被層を可塑化し平滑な加熱仕上げ
表面に圧接して乾燥するリウエツトキヤスト法
(例えば米国特許2759847号)(3)湿潤塗被層をゲル
状態に変え、平滑な加熱仕上げ表面に圧接して乾
燥するゲルキヤスト法(例えば特公昭38−15751
号、米国特許3377192号)等の方法が知られてい
る。 これらはいずれも鉱物質顔料及び接着剤を主体
とする塗被層が水を含んで可塑状態にある間に加
熱された仕上げ面に圧接して乾燥する点に於て原
理的に共通する方法を用している。このため塗被
層に含まれる水分を仕上げ面に圧接している間に
かなりの程度まで乾燥固化しなければならないた
めに製造速度が一般の顔料塗被紙に比べ、数十分
の一程度と数段遅くなつているのが現状である。 更に、従来高光沢度の顔料塗被紙を高速度で得
るための方法として、乾燥状態あるいはわずかに
含水状態の塗被紙を加熱されたロールないしドラ
ムを有するグロスカレンダー装置、あるいはスー
パーカレンダー装置等のロールニツプに強圧下で
通紙する方法が知られている。 スーパーカレンダー装置の使用は比較的高ニツ
プ圧力200Kg/cm前後の圧力で、スチール仕上げ
ロールの温度は70℃前後である。 本加工は塗被紙を圧縮し、そして緻密化する欠
点を有する。一方グロスカレンダーとして知られ
ている、熱カレンダー加工により紙面を仕上げる
方法は、紙面に可塑性の一時的状態を起させる温
度条件下で研摩仕上げドラムに塗被紙を押し付け
て仕上げるものである。スーパーカレンダーに比
較して嵩高い紙質を与えよつて不透明度の優れた
印刷用塗被紙が得られる。 グロスカレンダーの圧力条件はスーパーカレン
ダーに比較して一般に低く、90Kg/cm前後であ
り、温度条件は150℃前後と高い条件で使われて
いるのが一般である。 以上の如き加熱カレンダーによる場合には、塗
被層表面の光沢及び平滑性は加熱、加圧下におけ
る塗被層の軟化変形(塑性変形)によつて得られ
るものであるから塗被層自体が加熱加圧によつて
塑性変化しやすくする事が望ましく、従つて、塗
被層中の接着剤は熱可塑性であつた方が加熱加圧
下に直ちに塑性変形して金属ロール等の仕上げ表
面を写し取り良好な光沢及び平滑性を与えるのに
有利である。反面塗被層表面が仕上げロール面に
粘着する傾向が次第に増大し、微小な異物の堆積
がやがて連続運転を不可能にしてしまう。このよ
うな粘着傾向を除くために、従来、ワツクス類、
脂肪類、脂肪酸類、石けん類、界面活性剤類、シ
リコーン樹脂類等の離型剤を塗料に配合するか、
又は仕上げロールに連続して塗布する事がしばし
ば行なわれるが、仕上げロール表面に次第に離型
剤が堆積し、過剰の離型剤皮膜を形成するため塗
被紙の光沢が著しく低下する。 又離型剤の添加量の適当なコントロールが非常
に困難であり、多量の離型剤の配合は印刷適性の
低下原因ともなり、必ずしも好ましい解決策では
ない。 一方より良い光沢、平滑性を得る為に、米国特
許2293278号及び特公昭51−25482号に、加熱カレ
ンダー前に塗被紙表面に水を与えニツプ間を通す
事が記載されているがこの方法によると、最適の
水量を与える事が困難であり、更に前述の加熱カ
レンダー汚れの傾向を増大させ好ましくない。 本発明の目的はより良い光沢、平滑性を有する
印刷用塗被紙を作業性よく製造する方法を提供す
るにある。 かくして本発明は主成分が塗被用顔料と親水性
接着剤よりなる水性塗被液に於いて、該接着剤が
主にガラス転移温度(以下Tgと記す)38℃以上
の重合体ラテツクスを含有する水性塗被液を、水
との接触時間5秒後のコブサイズ度が0.4〜10
g/m2である原紙又は下塗り紙に塗布し乾燥後そ
の塗被面を、該重合体のTg以上でグロスカレン
ダーに圧接し、より高い光沢、平滑性を有する印
刷用塗被紙を製造しようとするものである。 本発明による原紙又は下塗紙のコブサイズ度を
限定する理由は以下の如くと考えられる。強光沢
を得る為に加熱面に瞬間的に圧接される際にその
塑性変形をより良く行なわしめる為には塗被層の
水分量が大きな要因である。勿論水分量の多い方
が変形に対して好ましい。しかし水分量が過剰で
あると加熱面への汚れが生じる。この水分量を圧
接時に効率よく適量塗層中に留まらせる事は、強
光沢面を作業性良く得る為に重要である。この目
的の為に原紙又は下塗紙の水との接触時間5秒後
のコブサイズ度を0.4〜10g/m2好ましくは2〜
7g/m2に限定する事は非常に有効である。 原紙及び下塗り紙の5秒後のコブサイズ度が10
g/m2を越える場合は加熱ニツプ間で塗層の塑性
変形が行なわれる間塗層中の水分が完全に留まら
ず、その結果、より良い光沢が得られない。一方
0.4g/m2よりも少ないコブサイズ度では、塗被
液中の接着剤の原紙への浸透が充分行なわれずに
塗被紙、膠着力に問題が生じる。 尚ここで云うコブサイズ度とはJIS.P.8140に示
される方法に準じ測定した値である。特に測定時
間を5秒と規定しているのは以下の如き理由によ
る。あまり長い測定時間でのコブサイズ度の場
合、測定値の差がつきにくくなり本発明でいう効
果との相関がとりにくい。この為その測定時間は
短かければ短い程良いがあまり短時間の場合、測
定誤差が大きく実用に適さない。 安定して測定が行なえ、本発明でいう効果との
相関がある測定時間として5秒間を定めている。 即ち、測定はJIS.P.8140と同一の方法であり、
水との接触時間だけ5秒間としている。 本発明におけるTgが38℃以上の熱可塑性合成
高分子エマルジヨン(重合体ラテツクス)とは、
ポリ酢酸ビニルエマルジヨン、スチレン−ブタジ
エン共重合体ラテツクス、スチレン−イソプレン
共重合体エマルジヨン、ポリスチレンエマルジヨ
ン、アクリル重合体エマルジヨン等を示すが、こ
れらに限定されるものではない。 Tgを38℃以上に限定する理由は特開昭49−
110906号で明らかな様に室温で被膜形成性がな
く、エマルジヨン粒子の不連続層を形成し、しか
る後キヤストドラム上で軟化せしめ光沢付けを行
なう事を目的としたものであり、一般に塗被紙に
使用されるTgの低い合成エマルジヨンを使用し
た場合、塗被後被膜形成性を有する為、キヤスト
ドラム上で軟化し圧着しても所望の強光沢は得ら
れいくいという理由による。 本発明の水性塗被液は上述の如き接着剤として
主にTgが38℃以上の重合体ラテツクスを用い、
他に用途に合めてTgが38℃以下の熱可塑性樹脂
及び熱硬化性樹脂を支障のない範囲において適宜
混合して使用できる。又更に用途に合わせて消泡
剤、抑泡剤、離型剤、増粘剤、流動変性剤、着色
剤等が適宜使用させる。 一方本発明において鏡面仕上げに用いられる加
熱カレンダー装置とは、グロスカレンダーやスー
パーカレンダー等の一般の光沢附与、平滑化装置
が考えられるが圧力が比較的低い事からカレンダ
ー汚れに有利である点、及び得られる塗被紙の品
質が嵩高くすぐれる事から特にグロスカレンダー
装置を用いる事が望ましい。 本発明の塗被液の紙への塗被は、塗被紙の製造
に一般に用いられている。エアーナイフコータ
ー、ロールコーター、ドクトルコーター、ブレー
ドコーター、ブラツシユコーター、カーテンコー
ター、バーコーター、グラビアコーター、チヤン
プレツクスコーター、サイズプレスコーター等の
塗被装置を設けたコーターにより一層あるいは、
多層に分けて塗被することが可能である。塗被量
は通常10〜40g/m2、好ましくは10〜30g/m2
ある。塗被後の乾燥は通常の乾燥方法、例えばガ
スヒーター、電気ヒーター、蒸気加熱ヒーター、
熱風加熱等の各種方式が用いられる。 以下に本発明の実施例を挙げて説明するが、こ
れらの例に限定されるものではない。尚実施例に
於て示す部、及び%は重量部及び重量%を意味す
る。 以下に実施例中の諸物性値の測定方法を示す。 (1) 白紙光沢度 光沢測定装置(日本理学KK製)により75゜及
び20゜光沢を測定した。% (2) 印刷光沢度 RI印刷適性試験器(明製作所製)により印
刷し乾燥後、光沢度測定装置(日本理学KK
製)にて60゜光沢を測定した。% (3) 平滑度 スムースター平滑度測定器(東英電子工業
KK製)により測定した。mmHg (4) 塗被紙表面強度 塗被紙の表面強度をRI印刷適性試験器(明
製作所)を用いて判定した。 乾:試料を一定のタツクをもつインキで印刷し
その試料表面を視感判定した。 湿:試料表面にごく少量の水を施し、直ちに一
定のタツクをもつインキで印刷し、その試料
表面を視感判定した。 5→1になる程表面強度は悪くなる。 実施例 1 カオリンクレー90部、沈降性炭酸カルシウム10
部からなる顔料をピロリン酸ソーダ0.2部によつ
て水中に分散させて固形分70%のクレースラリー
を調整した。このものにリン酸エステル化澱粉3
部、ガラス転移温度60℃のスチレン−ブタジエン
ラテツクスを15部加え、充分撹伴して全固形分含
有率が62%になるような塗被液を得た。 この塗被液を、内添サイズ剤量を変えてその5
秒後のコブサイズ度が(A)0.2g/m2 (B)1.5g/m2
(C)6g/m2 (D)9.8g/m2 (E)15g/m2である
80g/m2の坪量の各原紙に乾燥固形分が各々16
g/m2となるようにブレードコーターにて塗布
し、120〜130℃に加熱されたエアーキヤツプドラ
イヤーにて乾燥後、ニツプ圧80Kg/cm、表面温度
130℃、速度120m/minの条件でグロスカレンダ
ー掛けを行い、5種類の塗被紙を得た。 得られた塗被紙の性質を表1に記載した。
The present invention relates to a manufacturing method capable of providing highly glossy coated paper having excellent printability stably and with high productivity. Conventionally, methods for producing highly glossy paper include (1) the wet cast method (for example, the
38-25160) (2) After drying the wet coating layer,
Rewet casting method (for example, US Patent No. 2759847), in which the coating layer is plasticized by rewetting and then dried by pressing it against a smooth heated surface (for example, US Pat. No. 2,759,847). Gel cast method in which pressure is applied to dry
Methods such as No. 1, US Pat. No. 3,377,192) are known. All of these methods have a common principle in that the coating layer, which is mainly composed of mineral pigments and adhesives, is dried by pressing it against a heated finished surface while it is in a plastic state due to water content. I am using it. For this reason, the moisture contained in the coating layer must be dried and solidified to a considerable extent while being pressed against the finished surface, so the manufacturing speed is only a few tenths of that of ordinary pigment-coated paper. The current situation is that it is several steps behind. Furthermore, as a conventional method for obtaining high-gloss pigment-coated paper at high speed, dry or slightly water-containing coated paper is processed using a gloss calendering device having heated rolls or drums, a supercalendering device, etc. A method is known in which paper is passed through a roll nip under strong pressure. The use of supercalender equipment is at a relatively high nip pressure of around 200Kg/cm and the temperature of the steel finishing roll is around 70℃. This process has the disadvantage of compressing and densifying the coated paper. On the other hand, a method of finishing paper by thermal calendering, known as gloss calendering, involves pressing the coated paper against an abrasive finishing drum under temperature conditions that induce a temporary plastic state in the paper. A coated paper for printing with superior opacity and a bulkier paper quality compared to supercalenders can be obtained. The pressure conditions for gloss calenders are generally lower than those for super calenders, around 90 kg/cm, and the temperature conditions are generally high, around 150°C. In the case of using a heating calender as described above, the gloss and smoothness of the coating layer surface are obtained by softening deformation (plastic deformation) of the coating layer under heating and pressure, so the coating layer itself is heated. It is desirable for the adhesive in the coating layer to be easily plastically deformed under pressure. Therefore, if the adhesive in the coating layer is thermoplastic, it will immediately plastically deform under heat and pressure, allowing it to copy the finished surface of a metal roll, etc. Advantageous in providing good gloss and smoothness. On the other hand, the tendency of the coating layer surface to stick to the finishing roll surface gradually increases, and the accumulation of minute foreign matter eventually makes continuous operation impossible. In order to eliminate this tendency to stick, waxes,
Add release agents such as fats, fatty acids, soaps, surfactants, and silicone resins to the paint, or
Alternatively, coating is often carried out continuously on a finishing roll, but the release agent gradually accumulates on the surface of the finishing roll, forming an excessive release agent film, which significantly reduces the gloss of the coated paper. In addition, it is very difficult to appropriately control the amount of release agent added, and adding a large amount of release agent may cause a decrease in printability, which is not necessarily a preferable solution. On the other hand, in order to obtain better gloss and smoothness, U.S. Pat. According to the above method, it is difficult to apply an optimum amount of water, and furthermore, the above-mentioned tendency for heating calender staining increases, which is undesirable. An object of the present invention is to provide a method for producing coated printing paper having better gloss and smoothness with good workability. Thus, the present invention provides an aqueous coating liquid whose main components are a coating pigment and a hydrophilic adhesive, in which the adhesive mainly contains a polymer latex having a glass transition temperature (hereinafter referred to as Tg) of 38°C or higher. The aqueous coating fluid has a bump size of 0.4 to 10 after 5 seconds of contact with water.
g/m 2 on base paper or undercoated paper, and after drying, the coated surface is pressed against a gloss calendar at a temperature higher than the Tg of the polymer to produce coated paper for printing with higher gloss and smoothness. That is. The reasons for limiting the knob size of the base paper or undercoated paper according to the present invention are considered to be as follows. The moisture content of the coated layer is a major factor in achieving better plastic deformation when it is instantaneously pressed against a heated surface to obtain strong gloss. Of course, the higher the moisture content, the better against deformation. However, if the amount of moisture is excessive, stains will occur on the heating surface. Efficiently retaining an appropriate amount of this moisture in the coating layer during pressure welding is important in order to obtain a highly glossy surface with good workability. For this purpose, the lump size of the base paper or undercoated paper after 5 seconds of contact with water is adjusted to 0.4 to 10 g/m2, preferably 2 to 10 g/m2.
Limiting it to 7g/m 2 is very effective. Cob size degree of base paper and undercoat paper after 5 seconds is 10
If it exceeds g/m 2 , the moisture in the intercoating layer, which undergoes plastic deformation between the heating nips, will not be completely retained, and as a result, better gloss will not be obtained. on the other hand
If the cob size is less than 0.4 g/m 2 , the adhesive in the coating liquid will not penetrate sufficiently into the base paper, causing problems in the adhesive strength of the coated paper. Incidentally, the degree of bump size mentioned here is a value measured according to the method shown in JIS.P.8140. In particular, the reason why the measurement time is specified as 5 seconds is as follows. If the degree of bump size is measured over a too long measurement time, it will be difficult to differentiate between the measured values and it will be difficult to correlate with the effect referred to in the present invention. Therefore, the shorter the measurement time, the better; however, if the measurement time is too short, the measurement error will be large and it is not suitable for practical use. Five seconds is defined as a measurement time that allows stable measurement and has a correlation with the effects referred to in the present invention. In other words, the measurement is the same method as JIS.P.8140,
The contact time with water is set to 5 seconds. In the present invention, the thermoplastic synthetic polymer emulsion (polymer latex) with a Tg of 38°C or higher means:
Examples include, but are not limited to, polyvinyl acetate emulsion, styrene-butadiene copolymer latex, styrene-isoprene copolymer emulsion, polystyrene emulsion, acrylic polymer emulsion, and the like. The reason for limiting Tg to 38℃ or higher is JP-A-49-
As is clear from No. 110906, it does not form a film at room temperature, and its purpose is to form a discontinuous layer of emulsion particles, which is then softened and glossed on a cast drum, and is generally used on coated paper. This is because when using a synthetic emulsion with a low Tg, which is used for coating, it has a film-forming property after coating, so even if it is softened and pressed on a cast drum, the desired strong gloss cannot be obtained. The aqueous coating liquid of the present invention mainly uses a polymer latex with a Tg of 38°C or higher as the adhesive as described above,
In addition, thermoplastic resins and thermosetting resins having a Tg of 38° C. or less can be appropriately mixed and used as long as there is no problem. Furthermore, antifoaming agents, foam inhibitors, mold release agents, thickeners, flow modifiers, coloring agents, etc. may be used as appropriate depending on the purpose. On the other hand, the heating calender device used for mirror finishing in the present invention may be a general glossing or smoothing device such as a gloss calender or a super calender, but the pressure is relatively low, so it is advantageous for preventing calendar stains. In particular, it is desirable to use a gloss calender device because the quality of the resulting coated paper is high and bulky. Coating paper with the coating liquid of the present invention is generally used in the production of coated paper. A coater equipped with a coating device such as an air knife coater, roll coater, doctor coater, blade coater, brush coater, curtain coater, bar coater, gravure coater, triplex coater, size press coater, etc.
It is possible to apply the coating in multiple layers. The coating amount is usually 10 to 40 g/m 2 , preferably 10 to 30 g/m 2 . Drying after coating is done using a normal drying method, such as a gas heater, electric heater, steam heater,
Various methods such as hot air heating are used. The present invention will be described below with reference to examples, but it is not limited to these examples. In addition, parts and percentages shown in Examples mean parts by weight and percentages by weight. Methods for measuring various physical property values in Examples are shown below. (1) White paper glossiness 75° and 20° gloss was measured using a gloss measuring device (manufactured by Nippon Rigaku KK). % (2) Printing glossiness After printing with an RI printing aptitude tester (manufactured by Mei Seisakusho) and drying, the glossiness measurement device (Nihon Rigaku KK) was used.
60° gloss was measured using % (3) Smoothness Smoother smoothness measuring device (Toei Electronics Industry Co., Ltd.)
(manufactured by KK). mmHg (4) Coated paper surface strength The surface strength of the coated paper was determined using an RI printability tester (Mei Seisakusho). Dry: A sample was printed with ink having a certain tack, and the surface of the sample was evaluated visually. Wet: A very small amount of water was applied to the surface of the sample, immediately printed with ink having a certain tack, and the surface of the sample was evaluated visually. As the ratio increases from 5 to 1, the surface strength becomes worse. Example 1 Kaolin clay 90 parts, precipitated calcium carbonate 10 parts
A clay slurry with a solids content of 70% was prepared by dispersing the pigment consisting of 1.0 parts in water with 0.2 parts of sodium pyrophosphate. This stuff contains 3 phosphate esterified starches.
15 parts of styrene-butadiene latex having a glass transition temperature of 60 DEG C. were added thereto and sufficiently stirred to obtain a coating liquid having a total solids content of 62%. This coating liquid was prepared by changing the amount of internal sizing agent.
The bump size after seconds is (A) 0.2g/m 2 (B) 1.5g/m 2
(C) 6g/m 2 (D) 9.8g/m 2 (E) 15g/m 2
Each base paper with a basis weight of 80 g/ m2 has a dry solids content of 16
g/m 2 with a blade coater, and dried with an air cap dryer heated to 120-130°C, with a nip pressure of 80 kg/cm and a surface temperature of
Gloss calendering was performed at 130° C. and a speed of 120 m/min to obtain five types of coated papers. The properties of the coated paper obtained are listed in Table 1.

【表】 表1に示す如くS−No.2、3、4の物質値、特
にS−No.3は優れ、本発明の効果は顕著である。 実施例 2 カオリンクレー90部、沈降性炭酸カルシウム10
部からなる顔料を、ピロリン酸ソーダ0.2部によ
つて水中に分散させ、固形分70%のクレースラリ
ーを調整した。このものにリン酸エステル化澱粉
3部、ガラス転移温度 (F)40℃ (G)0℃のスチレ
ン−ブタジエンラテツクス15部加え、充分撹伴し
て全固形分含有率が62%になるような塗被液を得
た。 この塗被液をカオリン50部、重質炭酸カルシウ
ム50部、酸化澱粉10部、スチレン−ブタジエンラ
テツクス15部なる組成を有する塗被液を下塗液と
して75g/m2原紙に片面6g/m2ゲートロールコ
ーターにて塗工した下塗り紙に乾燥固形分が16
g/m2となるようにブレードコーターにて塗布
し、120〜130℃に加熱されたエアーキヤツプドラ
イヤーにて乾燥後ニツプ圧80Kg/cm、表面温度
130℃、速度120m/minの条件でグロスカレンダ
ー掛けを行い、塗被紙を得た。尚使用した下塗紙
の5秒後のコブサイズ度は7g/m2であつた。 得られた塗被紙の性質を表2に記載した。
[Table] As shown in Table 1, the material values of S-No. 2, 3, and 4, especially S-No. 3, are excellent, and the effect of the present invention is remarkable. Example 2 Kaolin clay 90 parts, precipitated calcium carbonate 10 parts
A clay slurry with a solids content of 70% was prepared by dispersing the pigment consisting of 1.0 parts in water with 0.2 parts of sodium pyrophosphate. To this, add 3 parts of phosphoric acid esterified starch and 15 parts of styrene-butadiene latex with a glass transition temperature (F) of 40°C (G) of 0°C, and stir thoroughly until the total solids content reaches 62%. A coating liquid was obtained. This coating liquid was applied as an undercoating liquid with a composition of 50 parts of kaolin, 50 parts of heavy calcium carbonate, 10 parts of oxidized starch, and 15 parts of styrene-butadiene latex to 75 g/m 2 of base paper, 6 g/m 2 on one side. The dry solid content of the base coated paper coated with a gate roll coater is 16
g/m 2 with a blade coater, and dried with an air cap dryer heated to 120-130℃, with a nip pressure of 80 kg/cm and a surface temperature of
Gloss calendering was performed at 130°C and a speed of 120 m/min to obtain coated paper. The nob size of the undercoated paper used after 5 seconds was 7 g/m 2 . The properties of the coated paper obtained are listed in Table 2.

【表】 表2より本発明の効果は明らかである。【table】 From Table 2, the effects of the present invention are clear.

Claims (1)

【特許請求の範囲】[Claims] 1 主成分が塗被用顔料と親水性接着剤よりなる
水性塗被液に於いて、該接着剤が主にガラス転移
温度38℃以上の重合体ラテツクスを含有する水性
塗被液を、水との接触時間5秒後のコブサイズ度
が0.4〜10g/m2である原紙又は下塗り紙に塗布
し乾燥後その塗被面を該重合体ラテツクスのガラ
ス転移温度以上でグロスカレンダーに圧接する事
を特徴とする印刷用強光沢紙の製造方法。
1. In an aqueous coating liquid whose main components are a coating pigment and a hydrophilic adhesive, the adhesive mainly contains a polymer latex with a glass transition temperature of 38°C or higher. It is characterized in that it is applied to a base paper or undercoated paper with a bump size of 0.4 to 10 g/m 2 after a contact time of 5 seconds, and after drying, the coated surface is pressed against a gloss calender at a temperature higher than the glass transition temperature of the polymer latex. A method for producing highly glossy printing paper.
JP715880A 1979-11-06 1980-01-24 Production of high gloss paper for printing Granted JPS56107098A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP715880A JPS56107098A (en) 1980-01-24 1980-01-24 Production of high gloss paper for printing
US06/203,223 US4317849A (en) 1979-11-06 1980-10-31 Process for producing high-gloss coated paper

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP715880A JPS56107098A (en) 1980-01-24 1980-01-24 Production of high gloss paper for printing

Publications (2)

Publication Number Publication Date
JPS56107098A JPS56107098A (en) 1981-08-25
JPS6410638B2 true JPS6410638B2 (en) 1989-02-22

Family

ID=11658257

Family Applications (1)

Application Number Title Priority Date Filing Date
JP715880A Granted JPS56107098A (en) 1979-11-06 1980-01-24 Production of high gloss paper for printing

Country Status (1)

Country Link
JP (1) JPS56107098A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5834198B2 (en) * 1976-07-08 1983-07-25 日本住宅公団 Sewage treatment equipment

Also Published As

Publication number Publication date
JPS56107098A (en) 1981-08-25

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