JPS5953956B2 - Manufacturing method of matte coated paper - Google Patents
Manufacturing method of matte coated paperInfo
- Publication number
- JPS5953956B2 JPS5953956B2 JP7449578A JP7449578A JPS5953956B2 JP S5953956 B2 JPS5953956 B2 JP S5953956B2 JP 7449578 A JP7449578 A JP 7449578A JP 7449578 A JP7449578 A JP 7449578A JP S5953956 B2 JPS5953956 B2 JP S5953956B2
- Authority
- JP
- Japan
- Prior art keywords
- coated paper
- paper
- gloss
- weight
- roll
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000007788 roughening Methods 0.000 claims description 26
- 239000000049 pigment Substances 0.000 claims description 17
- 238000000576 coating method Methods 0.000 claims description 16
- 239000011248 coating agent Substances 0.000 claims description 15
- 230000003746 surface roughness Effects 0.000 claims description 13
- 239000004816 latex Substances 0.000 claims description 10
- 229920000126 latex Polymers 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 9
- 239000000853 adhesive Substances 0.000 claims description 8
- 230000001070 adhesive effect Effects 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 3
- 238000007639 printing Methods 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 229920002472 Starch Polymers 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 150000001993 dienes Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- -1 lake Substances 0.000 description 2
- 238000013441 quality evaluation Methods 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229910000967 As alloy Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 108010058643 Fungal Proteins Proteins 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000004826 Synthetic adhesive Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000000227 bioadhesive Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 description 1
- 235000010261 calcium sulphite Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 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
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 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 1
- 239000012669 liquid formulation Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 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
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229940050271 potassium alum Drugs 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000001040 synthetic pigment Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Paper (AREA)
Description
【発明の詳細な説明】
本発明は艶消し塗被紙の製造方法に関し、特に白紙光沢
は低いが印刷後のインキ光沢が高く、しかもインキ受理
性の良好な艶消し塗被紙の製造方法に関するものである
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing matte coated paper, and in particular to a method for producing matte coated paper which has low white paper gloss but high ink gloss after printing and has good ink receptivity. It is something.
艶消し塗被紙は高度の光沢を有する塗被紙に比較して上
品で落ちついたイメージを与えるため、本文用紙のよう
な単色印刷物から各種多色印刷物まで塗被紙の重要なグ
レードの1つとして汎用されている。Matte coated paper gives an elegant and calm image compared to highly glossy coated paper, so it is one of the important grades of coated paper for everything from monochrome prints such as text paper to various multicolor prints. It is commonly used as.
しかし、かかる艶消し塗被紙は白紙光沢を下げるために
、通常の印刷用塗被紙に用いられる顔料より比較的粗に
顔料を多量に配合した塗液を基紙に塗布しており、しか
も平滑化のためのキヤレンダー処理も極く軽度ないしは
全<行つていない為インキの受理性が悪く、インキ平滑
性が悪いために印刷後のインキ光沢が低い欠点を有して
いる。このような欠点を改良するために、例えば特公昭
47−85号には硬質粗面化ロールをプラスチック製の
弾性ローールから成るキヤレンダーで塗被紙を処理する
方法が提案されている。However, in order to reduce the gloss of the white paper, such matte coated paper is coated with a coating liquid containing a relatively coarser amount of pigment than that used in ordinary coated printing paper, and moreover, Calender treatment for smoothing is either very light or not performed at all, resulting in poor ink receptivity and poor ink smoothness, resulting in low ink gloss after printing. In order to improve these drawbacks, for example, Japanese Patent Publication No. 47-85 proposes a method of treating coated paper with a calender consisting of a hard roughening roll and an elastic roll made of plastic.
しかしこのようなキヤレンダーを用いても、平滑性を良
くするために粗面化ロールの表面粗さを細かくすると白
紙光沢が著しく上昇してしまい、逆に粗面化ロールの表
面粗さを粗くすると充分な平滑性が得られず結果的にイ
ンキ受理性インキ平滑性が悪く、印刷後のインキ光沢の
低い艶消し塗被紙しか得られないのが現状である。本発
明者等は、かかる現状に鑑み艶消し塗被紙の塗液の組成
、および粗面化処理条件について鋭意研究した結果、従
来、軽いキヤレンダー掛けで高度の白紙光沢が得られる
ため艶消し塗被紙には用いられていない顔料であるサチ
ンホワイトの優フれた性質を、特定の粗面化処理によつ
て有効に利用することに着目し本発明を達成するに至つ
た。However, even if such a calender is used, if the surface roughness of the roughening roll is made finer to improve smoothness, the white paper gloss will increase significantly, and conversely, if the surface roughness of the roughening roll is made rougher, At present, sufficient smoothness cannot be obtained, resulting in poor ink receptivity and ink smoothness, and only matte coated paper with low ink gloss after printing can be obtained. In view of the current situation, the present inventors conducted intensive research on the composition of the coating liquid for matte coated paper and the roughening treatment conditions. The present invention was achieved by focusing on the effective use of the excellent properties of Sachin White, a pigment that is not used in paper coverings, through a specific surface roughening treatment.
本発明の目的は従来技術の欠点を改良し、JISP−8
142に基き測定される白紙光沢は10〜40%と低い
が印刷後のインキ光沢が高く、しかも優5れたインキ受
理性を有する艶消し塗被紙の製造方法を提供することで
ある。The purpose of the present invention is to improve the drawbacks of the prior art and to comply with JISP-8 standards.
The object of the present invention is to provide a method for producing a matte coated paper which has a low white paper gloss of 10 to 40% as measured based on 142, but has a high ink gloss after printing and has excellent ink receptivity.
本発明のかかる目的は、(a)3〜25重量%のサチツ
ボワイドを含む塗被紙用顔料と、(b)接着剤を主成分
とする塗液を基紙に塗被乾燥して得られる塗被紙を、J
ISBO65lで定義される表面粗さ(Rmax)が1
.2〜20μである硬質粗面化ロールにより処理するこ
とによつて達成される。The object of the present invention is to coat a base paper with a coating liquid containing (a) a pigment for coated paper containing 3 to 25% by weight of Sachitsubo Wide and (b) an adhesive and drying it. cover paper, J
Surface roughness (Rmax) defined by ISBO65l is 1
.. This is achieved by processing with a hard roughening roll having a roughness of 2 to 20 microns.
本発明において用いられるサチンホワイトとは、一般に
スルフオアルミン酸カルシウムとして知られ、石灰乳と
硫酸バンドあるいはカリ明バン等を反応させて得られる
針状あるいは板状の合成顔料であり、炭酸カルシウム、
塩化カルシウム、硅素、亜鉛等の一種以上の化合物を含
むものをも包含するものである。Sachin white used in the present invention is generally known as calcium sulfoaluminate, and is an acicular or plate-like synthetic pigment obtained by reacting milk of lime with sulfuric acid, potassium alum, etc.
It also includes those containing one or more compounds such as calcium chloride, silicon, and zinc.
サチンホワイトを塗被層中に含有する塗被紙はキヤレン
ダ一掛けによつて容易に高度の白紙光沢が賦与されるた
め、通常サチンホワイトは高度の白紙光沢を有する塗被
紙用の顔料としては用いられているが、艶消し塗被紙に
は使用されていない。本発明においてはかかるサチンホ
ワイト・を他の通常の塗被紙用顔料と特定の割合で併用
し、しかも得られた塗被紙を特定の条件下で粗面化処理
することによつて塗被紙に高度の白紙光沢を賦与するこ
となく白色度、平滑度、印刷後のインキ光沢さらにはイ
ンキ受理性を改善するものである。Coated paper containing Sachin White in its coating layer can easily be given a high white gloss by applying a calender, so Sachin White is usually not used as a pigment for coated papers with a high white gloss. used, but not for matte coated paper. In the present invention, such Sachin White is used in combination with other ordinary pigments for coated paper in a specific ratio, and the coated paper obtained is subjected to surface roughening treatment under specific conditions. It improves whiteness, smoothness, ink gloss after printing, and ink receptivity without imparting a high degree of white gloss to paper.
而してサチンホワイトはその配合割合が全顔料の3重量
%より少ないと得られる塗被紙のインキ光沢、インキ受
理性の改善効果において不充分であり、逆に25重量%
を越えると本発明の特殊な粗面化処理方法をもつてして
も得られる塗被紙の白紙光沢が40%以上になつてしま
うため、全顔料の3〜25重量%、好ましくは5〜15
重量%を占めるよ.うな割合で配合される。本発明にお
いてサチンホワイトと併用される塗被紙用顔料としては
、例えばカオリン、クレー、炭酸カルシウム、酸化チタ
ン、水酸化アルミニウム、酸化亜鉛、硫酸バリウム、硫
酸カルシウム、j亜硫酸カルシウム、タルク、シリカ、
活性白土、酸性白土、珪素土、レーキ、プラスチツクピ
グメント等が挙げられる。However, when the proportion of Sachin White is less than 3% by weight of the total pigment, it is insufficient in improving the ink gloss and ink receptivity of coated paper;
If it exceeds 3 to 25% by weight, preferably 5 to 25% by weight of the total pigment, the white paper gloss of the coated paper obtained even with the special surface roughening treatment method of the present invention will be 40% or more. 15
It accounts for % by weight. It is mixed in the same ratio. Pigments for coated paper used in combination with Sachin White in the present invention include, for example, kaolin, clay, calcium carbonate, titanium oxide, aluminum hydroxide, zinc oxide, barium sulfate, calcium sulfate, calcium sulfite, talc, silica,
Examples include activated clay, acid clay, silicon clay, lake, and plastic pigment.
本発明において用いられる接着剤としては、カゼイン、
大豆蛋白、酵母蛋白、澱粉、酸化澱粉、tエステル澱粉
、エーテル澱粉、カチオン澱粉、酵素変性澱粉、などの
変性澱粉、セルロース誘導体等の天然接着剤およびスチ
レン・ブタジエン系共重合体、メチルメタクリレート・
ブタジエン系共重合体などの共役ジエン系重合体ラテツ
クス、アクリル酸エステル、メタクリル酸エステル重合
体ないしは共重合体などのアクリル系重合体ラテツクス
、エチレン・酢酸ビニル共重合体などの酢酸ビニル系重
合体ラテツクス、ポリビニルアルコール等の合成接着剤
が挙げられる。The adhesive used in the present invention includes casein,
Modified starches such as soybean protein, yeast protein, starch, oxidized starch, t-ester starch, ether starch, cationic starch, enzyme-modified starch, natural adhesives such as cellulose derivatives, styrene-butadiene copolymers, methyl methacrylate, etc.
Conjugated diene polymer latex such as butadiene copolymer, acrylic polymer latex such as acrylic acid ester, methacrylic acid ester polymer or copolymer, vinyl acetate polymer latex such as ethylene/vinyl acetate copolymer and synthetic adhesives such as polyvinyl alcohol.
本発明においては、これらの接着剤の1種以上が一般に
顔料100重量部に対して3〜30重量部の割合で配合
されるが、本発明者等の検討によれば特に最低造膜温度
が20℃以上である重合体ラテツクスを特定の割合で用
いた場合には本発明の効果が顕著に得られることが明ら
かとなつた。即ち、一般に、接着剤として重合体ラテツ
クスを用いた塗被紙は印刷によつてインキ光沢の高い印
刷物を与えるが、反面キヤレンダ一掛けによつて白紙光
沢も容易に高くなる為、艶消し塗被紙においては以下に
説明する本発明の特殊な粗面化処理法によつても、なお
粗面化ロールの注意深い温度コントロールや比較的粗い
顔料の塗料への配合を必要とするものである。然に、2
0℃以上の最低造膜温度を有する重合体ラテツクスを特
定の割合で用いた場合には、白紙光沢を高くすることな
く印刷後のインキ光沢及びインキ受理性が効率良く改善
されることが明らかとなつた。かかる20℃以上の最低
造膜温度を有する重合体ラテツクスの使用割合は、顔料
100重量部に対して3重量部より少ないと印刷後のイ
ンキ光沢、インキ受理性に対する改善効果が少なく、又
25重量部を越えると白紙光沢が出易くなる為3〜25
重量部、より好ましくは5〜15重量部の範囲で使用す
るのが望ましい。最低造膜温度が20℃以上である重合
体ラテツクスとしては、I5〜30重量%の共役ジエン
、Ii全単量体の少なくとも2重量%を構成し得るメタ
クリル酸を含む2〜15重量%のエチレン性不飽和力ル
ボン酸とIii残部を形成するiおよびIiと共重合可
能なエチレン性不飽和単量体から成る共重合体ラテツク
スが例示される。In the present invention, one or more of these adhesives is generally blended at a ratio of 3 to 30 parts by weight per 100 parts by weight of the pigment, but according to studies by the present inventors, the minimum film forming temperature is particularly high. It has become clear that the effects of the present invention can be significantly obtained when a polymer latex having a temperature of 20° C. or higher is used in a specific ratio. That is, coated paper using polymer latex as an adhesive generally gives prints with high ink gloss when printed, but on the other hand, the gloss of the white paper can easily increase with one coat of calender, so it is difficult to coat with a matte coating. Even with the special roughening treatment method of the present invention described below, paper still requires careful temperature control of the roughening roll and the incorporation of relatively coarse pigments into the paint. Naturally, 2
It is clear that when a specific ratio of polymer latex having a minimum film-forming temperature of 0°C or higher is used, the ink gloss and ink receptivity after printing can be efficiently improved without increasing the white paper gloss. Summer. If the proportion of the polymer latex having a minimum film-forming temperature of 20° C. or higher is less than 3 parts by weight based on 100 parts by weight of pigment, the effect of improving ink gloss and ink receptivity after printing will be small; 3 to 25, as white paper tends to become glossy if it exceeds 3 to 25%.
It is desirable to use it in parts by weight, more preferably in the range of 5 to 15 parts by weight. A polymer latex having a minimum film forming temperature of 20° C. or higher includes 5 to 30% by weight of conjugated diene I, and 2 to 15% by weight of ethylene containing methacrylic acid that may constitute at least 2% by weight of the total monomers. An example is a copolymer latex consisting of an ethylenically unsaturated monomer copolymerizable with the ethylenically unsaturated carboxylic acid and i and Ii forming the remainder Iiii.
なお、上記1成分の共役ジエンとしてはブタジエン、イ
ソプレン、クロロプレンなどが、Ii成分のメタクリル
酸以外のエチレン性不飽和カルボン酸としてはアクリル
酸、クロトン酸、イタコン酸、フマル酸、マレイン酸な
どのモノあるいはジカルボン酸が、さらにIii成分の
エチレン性不飽和単量体としてはスチレン、α−メチル
スチレン、ジビニルベンゼンなどの芳香族ビニル化合物
、メチルアクリレート、エチルアクリレート、ブチルア
クリレート、メチルメタクリレート、エチルメタタリレ
ートなどのエチレン性不飽和カルボン酸エステルアクリ
ルアミド、シアン化ビニル単量体等が例示される。The above-mentioned conjugated dienes as one component include butadiene, isoprene, chloroprene, etc., and the ethylenically unsaturated carboxylic acids other than methacrylic acid as component Ii include monomers such as acrylic acid, crotonic acid, itaconic acid, fumaric acid, and maleic acid. Alternatively, the dicarboxylic acid is further used as the ethylenically unsaturated monomer of component III, such as aromatic vinyl compounds such as styrene, α-methylstyrene, and divinylbenzene, methyl acrylate, ethyl acrylate, butyl acrylate, methyl methacrylate, and ethyl methacrylate. Examples include ethylenically unsaturated carboxylic acid esters such as acrylamide and vinyl cyanide monomers.
また本発明において用いられる塗液の調製に際しては分
散剤、流動変性剤、消泡剤、着色剤など通常の塗被紙用
顔料に配合される各種助剤も必要に応じて適宜配合し得
ることは当然である。本発明においては上記の如く、(
a)3〜25重量%のサチンホワイトを含む塗被紙用顔
料と、(b)接着剤を主成分とする塗液を基紙の片面な
いしは両面に塗被乾燥するものであるが、塗被量、塗被
方式、乾燥方式については特に限定されず、一般の・塗
被紙製造の方式に従つて片面あたりおよそ6〜40g/
M2の塗被量になるよう例えばブレードコーター、エヤ
ーナイフコーター バーコータ一、チヤンプレツクスコ
ータ一、ロールコーター、サイズプレスコーター等の塗
工機によつて単層ないし4は多層に塗被され、およそ3
〜9%の紙水分まで乾燥されて巻取られる。In addition, when preparing the coating liquid used in the present invention, various auxiliary agents such as dispersants, flow modifiers, antifoaming agents, colorants, etc., which are usually added to pigments for coated paper, may be appropriately added as necessary. Of course. In the present invention, as described above, (
A coating liquid containing a) a pigment for coated paper containing 3 to 25% by weight of satin white and (b) an adhesive is applied to one or both sides of the base paper and dried. There are no particular limitations on the amount, coating method, and drying method, and approximately 6 to 40 g per side can be applied according to the general coated paper manufacturing method.
4 is coated in a single layer or in multiple layers using a coating machine such as a blade coater, an air knife coater, a bar coater, a chain coater, a roll coater, or a size press coater to obtain a coating amount of M2. 3
Dry to ~9% paper moisture and roll.
なお、上記の各種塗工機のうちでもブレードコーターは
特に上品な印刷物となる艶消し塗被紙を与えるためより
好ましく用いられる。本発明においては、かくして得ら
れた塗被紙を特定の表面粗さを有する硬質粗面化ロール
で処理するものであるが、粗面化ロールのの表面粗さが
JISBO65lで定義されるRmaxで1.2μより
細かいと処理後の塗被紙の白紙光沢が容易に40%を越
えてしまい、逆に20μより粗いと紙表面の平滑性が低
下して印刷後のインキ光沢が低くなるさめ、1.2〜2
0μの範囲内、より好ましくは4〜12μの表面粗さを
有する粗面化ロールで処理する必要がある。Among the above-mentioned various coating machines, the blade coater is more preferably used because it provides matte coated paper that produces particularly elegant printed matter. In the present invention, the coated paper thus obtained is treated with a hard roughening roll having a specific surface roughness, and the surface roughness of the roughening roll is Rmax defined by JISBO65l. If it is finer than 1.2μ, the white paper gloss of the coated paper after treatment will easily exceed 40%, while if it is coarser than 20μ, the smoothness of the paper surface will decrease and the ink gloss after printing will decrease. 1.2-2
It is necessary to process with a roughening roll having a surface roughness in the range of 0μ, more preferably between 4 and 12μ.
一般にかかる硬質粗面化ロールによる塗被紙の処理は、
塗被紙を硬質粗面化ロールと、紙、コツトン、アスベス
ト、ウール、プラスチツク等から成る弾性ロールで形成
されるニツプ中に通紙することによつて行なわれるが、
本発明においても上記の如き特定の表面粗さを有する硬
質粗面化ロールと弾性ロールで形成されるニップ沖に上
記の塗被紙を通紙する方法で粗面化処理が行なわれる。Generally, the treatment of coated paper with such hard roughening rolls is as follows:
This is done by passing the coated paper through a nip formed by a hard roughened roll and an elastic roll made of paper, cotton, asbestos, wool, plastic, etc.
In the present invention, the surface roughening treatment is also carried out by passing the above-mentioned coated paper through a nip formed by a hard roughening roll and an elastic roll having the above-mentioned specific surface roughness.
この際特公昭47−85号に記載されるような2本のプ
ラスチツク製の弾性ロールの両側に上記特定の表面粗さ
を有する2本の硬質粗面化ロールを配置したキヤレンダ
一は好ましい実施態様として本発明に適用される。本発
明の所望の効果を得るためには、硬質粗面化ロールで塗
被紙を処理する際の粗面化ロールの口ール温度も重要な
フアクタ一である。In this case, a preferred embodiment is a calender as described in Japanese Patent Publication No. 47-85, in which two hard surface roughening rolls having the above-mentioned specific surface roughness are arranged on both sides of two elastic rolls made of plastic. It is applied to the present invention as follows. In order to obtain the desired effects of the present invention, the mouth temperature of the roughening roll when treating coated paper with the hard roughening roll is also an important factor.
通常、印刷用塗被紙においては60℃以上のロール温度
でキヤレンダ一処理されるのが一般であるが、本発明の
艶消し塗被紙においては55℃以下、より好ましくは4
5℃以下のロール温度で処理するのが望ましい。その為
必要に応じてロール冷却装置を取り付けるなどの調節も
行なわれる。また、加圧条件は塗被紙の塗液配合、粗面
化ロールの表面粗さ、ロール温度および艶消し塗被紙の
所望する品質設定等に応じて適宜調節されるが、一般に
粗面化処理後の塗被紙の密度が0.8〜1.25g/C
nl3になるように調節するのが望ましい。Generally, coated paper for printing is subjected to calendering treatment at a roll temperature of 60°C or higher, but the matte coated paper of the present invention is subjected to a calendering process at a roll temperature of 55°C or lower, more preferably 4°C.
It is desirable to process at a roll temperature of 5°C or less. For this reason, adjustments such as installing a roll cooling device are made as necessary. In addition, the pressurizing conditions are adjusted as appropriate depending on the coating liquid formulation of the coated paper, the surface roughness of the roughening roll, the roll temperature, and the desired quality setting of the matte coated paper, but in general, roughening The density of coated paper after treatment is 0.8-1.25g/C
It is desirable to adjust it so that it becomes nl3.
なお、本発明で用いられる硬質粗面化ロールは前述の如
き特定の表面粗さを有する限り特に材質等については限
定されないが、一般に合金チルトロール、鋼鉄製ロール
などの金属ロールをサンドブラスト法、腐食法などによ
つて粗面化したロールが好ましく用いられる、また必要
に応じてクロムメツキ処理をしたロールも用いらろる。
かくして得られる本発明の艶消し塗被紙は、サチンホワ
イトの優れた性質が特定の粗面化処理によつて有効に活
用されているため、白紙光沢が充分に低い反面印刷後の
インキ光沢は高くしかもインキ受理性に優れており、上
品でかつ見栄えのする印刷物を提供することができる。The material of the hard roughened roll used in the present invention is not particularly limited as long as it has a specific surface roughness as described above, but generally metal rolls such as alloy tilt rolls and steel rolls are processed by sandblasting or corrosion. A roll whose surface has been roughened by a method such as a method is preferably used, and a roll which has been subjected to a chrome plating treatment can also be used if necessary.
The thus obtained matte coated paper of the present invention effectively utilizes the excellent properties of Sachin White through a specific surface roughening treatment, so while the white paper gloss is sufficiently low, the ink gloss after printing is low. It is expensive and has excellent ink receptivity, and can provide printed matter that is elegant and has a good appearance.
以下に本発明をさらに具体的に説明するために、実施例
を記載するが、勿論これらに限定されるものではない。Examples will be described below to further specifically explain the present invention, but the present invention is of course not limited to these.
なお、特に断らない限り「部」および「%」はそれぞれ
「重量部」および「重量%」を示す。実施例 1〜5、
比較例 1,2
第1表に示すような割合で配合した塗被紙用顔料と接着
剤を主成分とする塗液を64g/M2の基紙の両面に、
片面当りの塗被量が乾燥重量で20g/M2となるよう
にコータースピード300m/Minのブレードコータ
ーで塗被し、紙水分が7%になるように乾燥して巻取つ
た。Note that unless otherwise specified, "parts" and "%" indicate "parts by weight" and "% by weight," respectively. Examples 1 to 5,
Comparative Examples 1 and 2 A coating liquid containing pigments for coated paper and adhesive as main components in the proportions shown in Table 1 was applied to both sides of a 64 g/M2 base paper.
The paper was coated with a blade coater at a coater speed of 300 m/min so that the coating amount per side was 20 g/M2 in terms of dry weight, and the paper was dried and wound up so that the paper moisture content was 7%.
得られた塗被紙を表面粗さ(Rmax)が8μである硬
質粗面化ロールを2本配した4段スーパーキヤレンダ一
に硬質粗面化ロールの温度30℃で、処理後の紙の密度
が1.18になるように通紙して艶消し塗被紙を得た。The obtained coated paper was transferred to a 4-stage super calender equipped with two hard roughening rolls with a surface roughness (Rmax) of 8μ at a temperature of 30°C of the hard roughening rolls. A matte coated paper was obtained by passing the paper so that the density was 1.18.
得られた艶消し塗被紙の品質評価を以下の方法で行いそ
の結果を第1表に併記した。The quality of the obtained matte coated paper was evaluated by the following method, and the results are also listed in Table 1.
(1)白紙光沢:JISP−8142に従い角度75゜
で測定した。(1) White paper gloss: Measured at an angle of 75° according to JISP-8142.
(2)白紙平滑性:東英電子(株)製平滑度測定器(ス
ムースタ一)により測定した。(2) Blank paper smoothness: Measured using a smoothness meter (Smoothta-1) manufactured by Toei Denshi Co., Ltd.
単位は(2)で値が小さい程平滑性が良い(3)インキ
光沢及びインキ受理性:ローランドオフセツト印刷機に
よつて5000枚/分のスピードで印刷した印刷物のイ
ンキ光沢を目視判定した。The unit is (2), and the smaller the value, the better the smoothness. (3) Ink gloss and ink receptivity: The ink gloss of printed matter printed at a speed of 5000 sheets/minute with a Roland offset printing machine was visually judged.
評価基準は以下の6段階とした。◎・・・◎″・・・O
・・・○″・・・△・・・×(優れている) (
劣つている)第1表の結果から明らかなように、本発明
の各実施例で得られた艶消し塗被紙は白紙光沢がいづれ
も10〜40%の範囲にあり、白紙平滑性も良好2で、
印刷後のインキ光沢が高くしかもインキ受理性が良く上
品で見栄えのする印刷物として仕上つた。The evaluation criteria were the following six levels. ◎・・・◎″・・・O
・・・○″・・・△・・・× (Excellent) (
As is clear from the results in Table 1, the matte coated papers obtained in each example of the present invention all had white paper gloss in the range of 10 to 40%, and white paper smoothness was also good. At 2,
The ink gloss after printing was high and the ink receptivity was good, resulting in an elegant and attractive printed matter.
実施例 6,7、比較例 3,4
第1表に示されるような表面粗さ(Rmax)を2有す
る硬質粗面化ロールを用いた以外は実施例2と同様にし
て艶消し塗被紙を製造し、品質評価テストを行つてその
結果を第1表に併記した。Examples 6 and 7, Comparative Examples 3 and 4 Matt coated paper was prepared in the same manner as in Example 2, except that a hard roughening roll having a surface roughness (Rmax) of 2 as shown in Table 1 was used. was manufactured and subjected to quality evaluation tests, and the results are also listed in Table 1.
第1表の結果から明らかなように比較例3では白紙光沢
が著しく高く艶消し塗被紙の範鴫から外れるものであつ
た。また比較例4は白紙光沢は低いものの白紙平滑性が
著しく悪く、印刷後のインキ光沢、インキ受理性も劣つ
ていた。実施例 8
ブレードコーターの代りにエヤーナイフコーターを用い
た以外実施例2と同様にして艶消し塗被紙を製造し、品
質評価テストを行つてその結果を第1表に記載した。As is clear from the results in Table 1, in Comparative Example 3, the white paper gloss was extremely high and fell outside the range of matte coated paper. Furthermore, in Comparative Example 4, although the white paper gloss was low, the white paper smoothness was extremely poor, and the ink gloss and ink receptivity after printing were also poor. Example 8 A matte coated paper was produced in the same manner as in Example 2 except that an air knife coater was used instead of the blade coater, and a quality evaluation test was conducted. The results are shown in Table 1.
比較例 5
第1表に示すような割合で配合した塗液をエヤーナイフ
コーターで塗被した以外は実施例2を同様にして塗被紙
を得た。Comparative Example 5 A coated paper was obtained in the same manner as in Example 2, except that a coating liquid formulated in the proportions shown in Table 1 was coated using an air knife coater.
得られた塗被紙をプレーンな表面を有するチルトロール
を2本配した4段スーパーキヤレンダ一で、チルトロー
ルの温度60℃で、処理後の紙の密度が1.18になる
ように通紙して艶消し塗被紙を得た。得られた艶消し塗
被紙の品質評価を同様に行つたところ白紙平滑性が著し
く悪く、印刷後のインキ光沢、インキ受理性も極めて劣
つている印刷物しか得られなかつた。The obtained coated paper was passed through a four-stage super calender equipped with two tilt rolls each having a plain surface at a temperature of 60° C. so that the density of the paper after treatment was 1.18. A matte coated paper was obtained. When the quality of the obtained matte coated paper was evaluated in the same manner, only printed matter was obtained which had extremely poor white paper smoothness and extremely poor ink gloss and ink receptivity after printing.
Claims (1)
紙用顔料と、(b)接着剤を主成分とする塗液を基紙に
塗被乾燥して得られる塗被紙を、JISB_0_6_5
_1で定義される表面粗さ(Rmax)が1.2〜20
μである硬質粗面化ロールにより処理することを特徴と
する艶消し塗被紙の製造方法。 2 接着剤として最低造膜温度20℃以上の重合体ラテ
ックスを塗被紙用顔料100重量部に対して3〜25重
量部含有することを特徴とする特許請求の範囲第1項記
載の艶消し塗被紙の製造方法。[Scope of Claims] 1. Obtained by coating a base paper with a coating liquid containing (a) a pigment for coated paper containing 3 to 25% by weight of satin white and (b) an adhesive and drying it. Coated paper, JISB_0_6_5
Surface roughness (Rmax) defined by _1 is 1.2 to 20
1. A method for producing matte coated paper, characterized in that the process is carried out using a hard surface roughening roll. 2. The matte according to claim 1, which contains 3 to 25 parts by weight of a polymer latex having a minimum film-forming temperature of 20° C. or more as an adhesive based on 100 parts by weight of a pigment for coated paper. Method of manufacturing coated paper.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7449578A JPS5953956B2 (en) | 1978-06-19 | 1978-06-19 | Manufacturing method of matte coated paper |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7449578A JPS5953956B2 (en) | 1978-06-19 | 1978-06-19 | Manufacturing method of matte coated paper |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS551359A JPS551359A (en) | 1980-01-08 |
| JPS5953956B2 true JPS5953956B2 (en) | 1984-12-27 |
Family
ID=13548931
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7449578A Expired JPS5953956B2 (en) | 1978-06-19 | 1978-06-19 | Manufacturing method of matte coated paper |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5953956B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02269896A (en) * | 1989-04-11 | 1990-11-05 | Kanzaki Paper Mfg Co Ltd | Coated paper manufacturing method |
-
1978
- 1978-06-19 JP JP7449578A patent/JPS5953956B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS551359A (en) | 1980-01-08 |
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