JP2003300388A - Lithographic printing plate material, method for manufacture thereof, and printing method - Google Patents
Lithographic printing plate material, method for manufacture thereof, and printing methodInfo
- Publication number
- JP2003300388A JP2003300388A JP2003025668A JP2003025668A JP2003300388A JP 2003300388 A JP2003300388 A JP 2003300388A JP 2003025668 A JP2003025668 A JP 2003025668A JP 2003025668 A JP2003025668 A JP 2003025668A JP 2003300388 A JP2003300388 A JP 2003300388A
- Authority
- JP
- Japan
- Prior art keywords
- printing plate
- plate material
- lithographic printing
- layer
- 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.)
- Pending
Links
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- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 125000006162 fluoroaliphatic group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000010979 ruby Substances 0.000 description 1
- 229910001750 ruby Inorganic materials 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- OKYDCMQQLGECPI-UHFFFAOYSA-N thiopyrylium Chemical compound C1=CC=[S+]C=C1 OKYDCMQQLGECPI-UHFFFAOYSA-N 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Photosensitive Polymer And Photoresist Processing (AREA)
- Materials For Photolithography (AREA)
- Manufacture Or Reproduction Of Printing Formes (AREA)
- Printing Plates And Materials Therefor (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は平版印刷版材料と前
記平版印刷版材料の製造方法およびそれを用いた印刷方
法に関する。TECHNICAL FIELD The present invention relates to a lithographic printing plate material, a method for producing the lithographic printing plate material, and a printing method using the same.
【0002】[0002]
【従来の技術】コンピューターの普及、デジタル技術の
普及に伴い平版印刷版の作製工程には、電子画像データ
に基づいて平版印刷版材料に直接描画する、コンピュー
ターツー プレートの技術(CTP)が普及しつつあ
る。これによりワークフローの簡略化、フィルム作製の
為のコスト削減が可能となった。2. Description of the Related Art With the spread of computers and digital technology, a computer-to-plate technology (CTP) for directly drawing on a planographic printing plate material based on electronic image data has become popular in the process of making a planographic printing plate. It's starting. This has made it possible to simplify the workflow and reduce the cost for film production.
【0003】また、近年、CTP普及と同期して印刷環
境のオフィス化が進み、オフィスでの省スペース化の要
望も高まりつつある。大日本スクリーン製造株式会社の
TruePressシステムやハイデルベルグPMT社
のクイックマスター46DIシステムなどの印刷機は印
刷機内に露光装置を具備し、オフラインのプレートセッ
ターを必要としないシステムであり、印刷機のコンパク
ト化が計られ、オフィスでの省スペース化に貢献してい
る(例えば、特許文献1参照。)。Further, in recent years, the office of the printing environment has been developed in synchronism with the spread of CTP, and the demand for space saving in the office is also increasing. Printing machines such as the TruePress system of Dainippon Screen Mfg. Co., Ltd. and the Quickmaster 46DI system of Heidelberg PMT have an exposure device inside the printing machine and do not require an offline platesetter. It contributes to space saving in the office (for example, refer to Patent Document 1).
【0004】これら印刷機に使用される平版印刷版材料
は何れもプラスチックフィルム支持体を有していて、こ
れら平版印刷材料はロール状シートからガイドロール等
搬送部材により誘導されて印刷機内に予め設置されてい
る版胴に供給されるが、搬送部材が印刷原版に悪影響を
及ぼすことがあった。具体的には、これら搬送部材が印
刷原版の表面を擦ることにより搬送キズを発生させ、印
刷物において画像欠陥を引き起こすことがしばしばであ
った。The planographic printing plate materials used in these printing machines all have a plastic film support, and these planographic printing materials are installed in advance in the printing machine by being guided from a roll-shaped sheet by a conveying member such as a guide roll. However, the transport member sometimes adversely affects the printing original plate. Specifically, these transport members often rub the surface of the printing original plate to generate transport scratches, often causing image defects in the printed matter.
【0005】クイックマスター46DIシステムはプレ
ステック社のパールドライプレートを平版印刷版材料と
して使用するシステムであるが、パールドライプレート
は基材上に親油性を有する層/光熱変換層/シリコーン
ゴム層を順次積層した形態となっており、このシリコー
ン層にキズが入るとその部分が地汚れになってしまうと
いう問題を抱えている。The Quickmaster 46DI system is a system in which a pearl dry plate manufactured by Prestec Co., Ltd. is used as a lithographic printing plate material. The pearl dry plate has a lipophilic layer / photothermal conversion layer / silicone rubber layer on a substrate. It has a form in which layers are sequentially laminated, and there is a problem in that if the silicone layer is damaged, that portion becomes scumming.
【0006】TruePressシステムは、三菱製紙
株式会社製のシルバーディジプレートを平版印刷版材料
として使用するシステムであるが、このシステムにおい
ては平版印刷版材料の搬送中にジャムを生じることもあ
り、この場合、印刷機を停止し、平版印刷版材料の排出
や再度、平版印刷版材料の設置を行わなければならず、
印刷の歩留まりを大きく悪化させてしまう。The TruePress system is a system that uses a silver digit plate manufactured by Mitsubishi Paper Mills, Ltd. as a lithographic printing plate material. In this system, a jam may occur during the transportation of the lithographic printing plate material. , The printing machine must be stopped, the planographic printing plate material must be discharged and the planographic printing plate material must be set again.
The printing yield is greatly deteriorated.
【0007】搬送ジャムを低減するためには、フィルム
裏面側にも摩擦を低減させるバックコート層の塗設が考
えられるが、平版印刷版材料作製の為に工程数が増え、
平版印刷版材料のコストが高価になってしまう等の問題
点がある。In order to reduce the conveyance jam, it is conceivable to apply a back coat layer on the back side of the film to reduce friction, but the number of steps is increased to prepare the planographic printing plate material,
There is a problem that the cost of the planographic printing plate material becomes high.
【0008】[0008]
【特許文献1】特開平10−272756号公報[Patent Document 1] Japanese Unexamined Patent Publication No. 10-272756
【0009】[0009]
【発明が解決しようとする課題】本発明の目的は、搬送
時の搬送キズや搬送不良がなく、画像欠陥が少なく、低
コストの平版印刷版材料とその製造方法を提供し、か
つ、前記平版印刷版材料を用いる印刷方法を提供するこ
とである。SUMMARY OF THE INVENTION It is an object of the present invention to provide a lithographic printing plate material which is free from transport scratches and transport defects during transport, has few image defects, and is low in cost, and a method for producing the same, It is to provide a printing method using a printing plate material.
【0010】[0010]
【課題を解決するための手段】本発明の上記目的は下記
の構成1〜13により達成された。The above objects of the present invention have been achieved by the following constitutions 1 to 13.
【0011】1.基材上に、少なくとも画像形成層を有
する平版印刷版材料の製造方法において、該基材上に該
画像形成層を有する側の第1最表面層が潤滑性成分を含
有するように調整する工程、ロール状に巻き取る工程と
を順次含むことを特徴とする平版印刷版材料の製造方
法。1. In the method for producing a lithographic printing plate material having at least an image forming layer on a substrate, the step of adjusting the first outermost surface layer on the side having the image forming layer on the substrate to contain a lubricating component A method for producing a lithographic printing plate material, comprising the steps of sequentially winding in a roll form.
【0012】2.前記ロール状に巻き取る工程の後に包
装材料で包装される工程を含むことを特徴とする前記1
に記載の平版印刷版材料の製造方法。2. 1. The method as described above, further comprising a step of wrapping with a wrapping material after the step of winding into a roll.
The method for producing a lithographic printing plate material as described in.
【0013】3.前記平版印刷版材料がロール状である
ことを特徴とする前記1または2に記載の平版印刷版材
料の製造方法。3. 3. The method for producing a lithographic printing plate material as described in 1 or 2 above, wherein the lithographic printing plate material is in a roll shape.
【0014】4.基材上に、少なくとも画像形成層を有
する平版印刷版材料において、該基材に該画像形成層を
有する側の第1最表面層が潤滑性成分を含有するように
調整する工程、次いで、ロール状に巻き取る工程を経て
製造されたことを特徴とする平版印刷版材料。4. In a lithographic printing plate material having at least an image forming layer on a substrate, a step of adjusting the first outermost surface layer on the side having the image forming layer of the substrate to contain a lubricating component, and then a roll A planographic printing plate material, which is manufactured through a process of winding into a shape.
【0015】5.前記ロール状に巻き取る工程の後に包
装材料で包装される工程を経て製造されたことを特徴と
する前記4に記載の平版印刷版材料。5. 5. The lithographic printing plate material as described in 4 above, which is produced through a step of packaging with a packaging material after the step of winding into a roll.
【0016】6.前記潤滑性成分が粒子形状であること
を特徴とする前記4または5に記載の平版印刷版材料。6. 6. The lithographic printing plate material as described in 4 or 5 above, wherein the lubricating component is in the form of particles.
【0017】7.前記第1最表面層が画像形成層であ
り、前記潤滑性成分が親油性の熱可塑性もしくは熱溶融
性粒子であることを特徴とする前記4〜6のいずれか1
項に記載の平版印刷版材料。7. Any one of the above 4 to 6, wherein the first outermost layer is an image forming layer, and the lubricating component is a lipophilic thermoplastic or thermofusible particle.
The planographic printing plate material as described in the above item.
【0018】8.基材と画像形成層との間に親水性層が
設けられていることを特徴とする前記4〜7のいずれか
1項に記載の平版印刷版材料。8. 8. The lithographic printing plate material as described in any one of 4 to 7 above, wherein a hydrophilic layer is provided between the substrate and the image forming layer.
【0019】9.基材がプラスチックよりなることを特
徴とする前記4〜8のいずれか1項に記載の平版印刷版
材料。9. 9. The lithographic printing plate material as described in any one of 4 to 8 above, wherein the base material is made of plastic.
【0020】10.ロール状に巻き取る工程前における
前記第1最表面層の静止摩擦係数が0.05以上2.0
未満であり、ロール状に巻き取る工程後の前記第1最表
面層とは反対側の第2最表面層の静止摩擦係数が共に
0.05以上2.0未満であることを特徴とする前記4
〜9のいずれか1項に記載の平版印刷版材料。10. The coefficient of static friction of the first outermost surface layer before the step of winding into a roll is 0.05 or more and 2.0 or more.
And the static friction coefficient of the second outermost surface layer on the side opposite to the first outermost surface layer after the step of winding into a roll is both 0.05 or more and less than 2.0. Four
10. The lithographic printing plate material as described in any one of 9 to 10.
【0021】11.ロール状に巻き取る工程前における
前記第1最表面層の静止摩擦係数が0.05以上2.0
未満、前記第2最表面層の静止摩擦係数が2.0以上
5.0以下であり、且つ、ロール状に巻き取る工程後の
前記第1最表面層および前記第2最表面層の静止摩擦係
数が共に0.05以上2.0未満であることを特徴とす
る前記10に記載の平版印刷版材料。11. The coefficient of static friction of the first outermost surface layer before the step of winding into a roll is 0.05 or more and 2.0 or more.
Less than, the coefficient of static friction of the second outermost surface layer is 2.0 or more and 5.0 or less, and the static friction of the first outermost surface layer and the second outermost surface layer after the step of winding into a roll. 11. The lithographic printing plate material as described in 10 above, wherein the coefficients are both 0.05 or more and less than 2.0.
【0022】12.ロール形状を有することを特徴とす
る前記4〜11のいずれか1項に記載の平版印刷版材
料。12. 12. The lithographic printing plate material as described in any one of 4 to 11 above, which has a roll shape.
【0023】13.前記1〜3のいずれか1項に記載の
製造方法により製造された平版印刷版材料Aもしくは、
前記4〜12のいずれか1項に記載の平版印刷版材料B
に、レーザー光により画像記録を行う工程、次いで、該
画像記録が行われた該平版印刷版材料Aまたは該平版印
刷版材料Bに、湿し水およびインクを供給して前記平版
印刷版材料A上または前記平版印刷版材料B上にインク
画像を形成する工程、形成された該インク画像をシート
状の基材に転写する工程を含むことを特徴とする印刷方
法。13. The planographic printing plate material A manufactured by the manufacturing method according to any one of 1 to 3 above, or
13. The planographic printing plate material B according to any one of 4 to 12 above.
To the planographic printing plate material A or the planographic printing plate material A on which the image recording is performed by supplying dampening water and ink to the planographic printing plate material A. A printing method comprising: a step of forming an ink image on or on the planographic printing plate material B; and a step of transferring the formed ink image to a sheet-shaped substrate.
【0024】以下、本発明を詳細に説明する。本発明は
上記問題を鑑みて考案されたもので、本発明者等は種々
検討の結果、基材上に、少なくとも画像形成層を有する
平版印刷版材料において、該基材体上に該画像形成層を
有する側の第1最表面層が潤滑性成分を含有するように
調製する工程、且つ、ロール状に巻き取る工程を経て製
造された平版印刷版材料は搬送ジャムが発生しにくく、
かつ搬送時に起こりうる搬送キズによる印刷物への影響
が著しく低減された印刷物を提供できることを見出し
た。すなわち、平版印刷版材料の画像形成層が塗設され
た側に潤滑性成分を含有した第1最表面層を有する平版
印刷版材料を、一旦ロール状に巻き取り、潤滑性成分を
もう一方の第2最表面層に十分に移行させることによ
り、表裏共に最表層の摩擦が低減され、搬送性が向上
し、搬送傷などの故障が発生しにくくなった。The present invention will be described in detail below. The present invention has been devised in view of the above problems, and as a result of various investigations by the present inventors, in a lithographic printing plate material having at least an image forming layer on a substrate, the image forming on the substrate was performed. The step of preparing the first outermost layer on the side having the layer so as to contain a lubricating component, and the planographic printing plate material produced through the step of winding into a roll is less likely to cause a conveyance jam,
It has also been found that it is possible to provide a printed matter in which the influence on the printed matter due to the scratches that may occur during transportation is significantly reduced. That is, a lithographic printing plate material having a first outermost surface layer containing a lubricating component on the side of the lithographic printing plate material coated with the image forming layer is once wound into a roll, and the lubricating component is added to the other side. By sufficiently migrating to the second outermost surface layer, the friction of the outermost surface layer on both the front and back sides was reduced, the transportability was improved, and troubles such as transport scratches were less likely to occur.
【0025】《潤滑性成分》本発明に係る潤滑性成分に
ついて説明する。<< Lubricating Component >> The lubricating component according to the present invention will be described.
【0026】基材上に該画像形成層を有する側の第1最
表面層に含有する潤滑性成分としては公知のものが利用
でき、脂肪酸、脂肪酸エステル、脂肪酸アミドなどワッ
クス類、ポリエチレングリコール類、(変性)シリコー
ン樹脂、(変性)シリコーンオイル、フッ素系化合物、
フッ化カーボンなどを挙げることができる。As the lubricating component contained in the first outermost surface layer on the side having the image forming layer on the substrate, known components can be used, and waxes such as fatty acids, fatty acid esters and fatty acid amides, polyethylene glycols, (Modified) silicone resin, (modified) silicone oil, fluorine compound,
Carbon fluoride etc. can be mentioned.
【0027】ワックス類としては、例えば、カルナバワ
ックス、蜜ろう、鯨ろう、木ろう、ホホバ油、ラノリ
ン、オゾケライト、パラフィンワックス、モンタンワッ
クス類、キャンデリンワックス、セレシンワックス、マ
イクロクリスタリンワックス、ライスワックスなどの天
然ワックス、ポリエチレンワックス、フィッシャートロ
プシュワックス、モンタンワックス誘導体、パラフィン
ワックス誘導体、マイクロクリスタリンワックス誘導
体、ステアリン酸、ステアリン酸アマイド等が挙げられ
る。Examples of the waxes include carnauba wax, beeswax, whale wax, wood wax, jojoba oil, lanolin, ozokerite, paraffin wax, montan wax, candelin wax, ceresin wax, microcrystalline wax, rice wax and the like. Natural wax, polyethylene wax, Fischer-Tropsch wax, montan wax derivative, paraffin wax derivative, microcrystalline wax derivative, stearic acid, stearic acid amide and the like.
【0028】シリコーン変性された樹脂としては、熱可
塑性樹脂や合成ゴムの一部をポリシロキサン鎖で修飾し
たものが挙げられ、修飾される樹脂としては、アクリル
系樹脂、スチレン−アクリル系樹脂、ポリエステル類、
ポリウレタン類、ポリエーテル類、ポリエチレン、ポリ
プロピレン、ポリスチレン、アイオノマー樹脂、酢酸ビ
ニル系樹脂、塩化ビニル系樹脂などが挙げられる。同じ
く修飾される合成ゴム類としては、ポリブタジエン、ポ
リイソプレン、ポリクロロプレン、スチレン−ブタジエ
ン共重合体、アクリル酸エステル−ブタジエン共重合
体、メタクリル酸エステル−ブタジエン共重合体、イソ
ブチレン−イソプレン共重合体、アクリロニトリル−ブ
タジエン共重合体、アクリロニトリル−イソプレン共重
合体、スチレン−イソプレン共重合体が挙げられる。Examples of the silicone-modified resin include a thermoplastic resin and a synthetic rubber in which a part of a synthetic rubber is modified with a polysiloxane chain. The modified resin includes an acrylic resin, a styrene-acrylic resin, and a polyester. Kind,
Polyurethanes, polyethers, polyethylene, polypropylene, polystyrene, ionomer resins, vinyl acetate resins, vinyl chloride resins and the like can be mentioned. Examples of the synthetic rubbers that are also modified are polybutadiene, polyisoprene, polychloroprene, styrene-butadiene copolymer, acrylic ester-butadiene copolymer, methacrylic acid ester-butadiene copolymer, isobutylene-isoprene copolymer, Examples thereof include acrylonitrile-butadiene copolymer, acrylonitrile-isoprene copolymer, and styrene-isoprene copolymer.
【0029】変性シリコーンオイルとしては、アミノ基
変性、エポキシ変性、カルボキシル基変性、フェノール
変性、ポリエーテル変性、高級アルコキシ変性のシリコ
ーンオイルが挙げられる。Examples of the modified silicone oil include amino group-modified, epoxy-modified, carboxyl group-modified, phenol-modified, polyether-modified and higher alkoxy-modified silicone oils.
【0030】フッ素系化合物としては、例えばフッ素系
界面活性剤:フルオロ脂肪族基を含むアクリレート、メ
タクリレート及び(ポリオキシアルキレン)アクリレー
トまたは(ポリオキシアルキレン)メタクリレートの共
重合体、特開昭62−170950号公報、特開昭62
−226143号公報、米国特許第3,787,351
号明細書等に記載のもの等が挙げられる。更に、特開昭
64−18142号公報記載の含フッ素アクリル系樹脂
等、特公平6−105351号公報、同8−3630号
公報、特開平3−172849号公報記載のフッ素系界
面活性剤、特開平1−260055号公報、同1−27
1478号公報、同4−63802号公報記載の化合物
等を好ましく使用することができる。Examples of the fluorine-based compound include a fluorine-based surfactant: a fluoroaliphatic group-containing acrylate, methacrylate and (polyoxyalkylene) acrylate or (polyoxyalkylene) methacrylate copolymer, JP-A-62-170950. Japanese Patent Laid-Open No. Sho 62
-226143, U.S. Pat. No. 3,787,351.
And the like described in the specification and the like. Further, fluorine-containing acrylic resins described in JP-A-64-18142, fluorine-containing surfactants described in JP-B-6-105351, JP-A-8-3630 and JP-A-3-172849, Kaihei 1-256055 and 1-27
The compounds described in Japanese Patent Nos. 1478 and 4-63802 can be preferably used.
【0031】(粒子形状の潤滑性成分)本発明において
潤滑性成分は粒子形状であることが好ましく、粒子形状
であることにより第1最表面層から脱離し、重ね合わさ
った反対側の第2最表面層に移行し易く、粒子状の方が
移行したときの摩擦力の低下が著しい。上述の潤滑性成
分のうち、常温で固体のものが粒子形状を形成するのに
有利であり、ワックス類、変性シリコーン樹脂などが利
用できる。(Lubricating component in particle form) In the present invention, the lubricating component is preferably in particle form, and because of the particle form, it is detached from the first outermost surface layer and the second outermost layer on the opposite side is overlapped. It is easy to transfer to the surface layer, and the particle-like one has a remarkable decrease in frictional force when transferred. Among the above-mentioned lubricating components, those which are solid at room temperature are advantageous for forming a particle shape, and waxes, modified silicone resins and the like can be used.
【0032】潤滑性成分を粒子形状にする方法である
が、上記材料をエマルジョン化することで達成できる。
エマルジョンに調製する方法は公知の方法が利用でき、
例えば、「分散技術総合資料集」(経営開発センター出
版部)等に記載された方法が利用できる。This is a method of forming the lubricating component into a particle shape, but it can be achieved by emulsifying the above material.
As a method for preparing an emulsion, a known method can be used,
For example, the method described in “Distribution Technology Comprehensive Material Collection” (Business Development Center Publishing Department) and the like can be used.
【0033】粒子形状をした潤滑性成分の粒径は第1最
表面から露出するように調整されていることが好まし
く、また、最表層表面からの露出不足を防止し、且つ、
搬送ジャムの低減、搬送傷の低減効果以外の印刷性能
(画像耐久性、感度など)を良好に保つ観点から、粒子
の平均粒径は0.1μm〜2.0μmの範囲が好まし
い。It is preferable that the particle diameter of the lubricating component in the form of particles is adjusted so as to be exposed from the first outermost surface, and the insufficient exposure from the outermost surface is prevented, and
The average particle size of the particles is preferably in the range of 0.1 μm to 2.0 μm from the viewpoint of maintaining good printing performance (image durability, sensitivity, etc.) other than the effects of reducing the transport jam and the transport scratches.
【0034】本発明に記載の効果(搬送ジャムの低減、
搬送傷の低減効果)を好ましく得る点から、本発明の平
版印刷版材料の第1最表面層に存在する潤滑性成分の量
は、1m2当たり、0.05g〜2.0gの範囲が好ま
しい。0.05gより少ないと、潤滑性成分の移行が不
十分となり、2.00gを超えると、保存後の印刷性能
が劣化することがある。また、第1最表面層の粒子形状
である潤滑性成分は、第1最表面層の全成分中の10質
量%〜100質量%であることが好ましい。Effects of the present invention (reduction of conveyance jam,
The amount of the lubricating component present in the first outermost surface layer of the lithographic printing plate material of the present invention is preferably in the range of 0.05 g to 2.0 g per 1 m 2 from the viewpoint of preferably obtaining the effect of reducing transport scratches). . If it is less than 0.05 g, the migration of the lubricating component will be insufficient, and if it exceeds 2.00 g, the printing performance after storage may deteriorate. Further, the lubricity component in the particle shape of the first outermost surface layer is preferably 10% by mass to 100% by mass in all the components of the first outermost surface layer.
【0035】潤滑性成分を含有する第1最表面層の静止
摩擦係数は0.05以上2.0未満であることが好まし
く、かつ反対側の第2最表面層の静止摩擦係数は、該平
版印刷版原版をロール状に巻き取った後に、巻き取る前
より低下し、更には、ロール巻き取り工程後におけるど
ちらの最表面層の静止摩擦係数も0.05以上2.0以
下になっていることが好ましい。The static friction coefficient of the first outermost surface layer containing the lubricating component is preferably 0.05 or more and less than 2.0, and the static friction coefficient of the second outermost surface layer on the opposite side is the lithographic plate. After winding the printing plate precursor in a roll shape, it is lower than before winding, and further, the static friction coefficient of either outermost layer after the roll winding step is 0.05 or more and 2.0 or less. It is preferable.
【0036】このような静止摩擦係数を確保することに
より、搬送時のジャムが低減出来、搬送傷による印刷物
の劣化も効果的に防ぐことができる。By securing such a coefficient of static friction, it is possible to reduce jams during transportation and effectively prevent deterioration of printed matter due to transport scratches.
【0037】本発明に係る静止摩擦係数の測定は、JI
S K 7125に規定された摩擦係数試験方法に準じ
て測定できる。ただし、測定条件下の環境は、25℃、
65%RHに調整される。The static friction coefficient according to the present invention is measured by JI
It can be measured according to the friction coefficient test method specified in SK 7125. However, the environment under the measurement conditions is 25 ℃,
Adjusted to 65% RH.
【0038】《画像形成層》本発明に係る画像形成層に
ついて説明する。<Image Forming Layer> The image forming layer according to the present invention will be described.
【0039】本発明に係る画像形成層としては、親油性
を有する熱可塑性もしくは熱溶融性粒子を主成分として
含有していることが好ましい。親油性を有し、且つ、粒
子形状を形成することで本発明請求項8の印刷方法を遂
行するのに有利である。すなわち、レーザー光源で画像
描画された部分は基材に溶融固定され、その他の部分
は、印刷機上でインクおよび湿し水により取り除かれる
為、自動現像機などの処理機を用いることなく製版が可
能となる。The image-forming layer according to the present invention preferably contains lipophilic thermoplastic or heat-meltable particles as a main component. Having the lipophilic property and forming a particle shape is advantageous for carrying out the printing method of claim 8 of the present invention. That is, the portion where the image is drawn by the laser light source is melted and fixed on the substrate, and the other portion is removed by the ink and the dampening water on the printing machine, so that the plate making can be performed without using a processor such as an automatic processor. It will be possible.
【0040】前述の親油性を有する熱可塑性もしくは熱
溶融性粒子を構成する材料としては熱可塑性樹脂、合成
ゴム、ワックス類が挙げられる。Examples of the material constituting the above-mentioned lipophilic thermoplastic or heat-meltable particles include thermoplastic resins, synthetic rubbers and waxes.
【0041】熱可塑性樹脂としては、アクリル系樹脂、
スチレン−アクリル系樹脂、ポリエステル類、ポリウレ
タン類、ポリエーテル類、ポリエチレン、ポリプロピレ
ン、ポリスチレン、アイオノマー樹脂、酢酸ビニル系樹
脂、塩化ビニル系樹脂などが挙げられる。As the thermoplastic resin, an acrylic resin,
Examples thereof include styrene-acrylic resins, polyesters, polyurethanes, polyethers, polyethylene, polypropylene, polystyrene, ionomer resins, vinyl acetate resins, and vinyl chloride resins.
【0042】合成ゴム類としては、ポリブタジエン、ポ
リイソプレン、ポリクロロプレン、スチレン−ブタジエ
ン共重合体、アクリル酸エステル−ブタジエン共重合
体、メタクリル酸エステル−ブタジエン共重合体、イソ
ブチレン−イソプレン共重合体、アクリロニトリル−ブ
タジエン共重合体、アクリロニトリル−イソプレン共重
合体、スチレン−イソプレン共重合体が挙げられる。The synthetic rubbers include polybutadiene, polyisoprene, polychloroprene, styrene-butadiene copolymer, acrylic ester-butadiene copolymer, methacrylic acid ester-butadiene copolymer, isobutylene-isoprene copolymer, acrylonitrile. -Butadiene copolymer, acrylonitrile-isoprene copolymer, styrene-isoprene copolymer are mentioned.
【0043】上述の熱可塑性樹脂もしくは合成ゴム類
は、融点もしくは軟化点が60℃以上であり、それ自身
をフィルム化したときにその水に対する接触角が50°
以上であるものが画像SN、感度の点で有利である。The above-mentioned thermoplastic resin or synthetic rubber has a melting point or softening point of 60 ° C. or higher, and when it is formed into a film, its contact angle with water is 50 °.
The above is advantageous in terms of image SN and sensitivity.
【0044】ワックス類としてはカルナバワックス、蜜
ろう、鯨ろう、木ろう、ホホバ油、ラノリン、オゾケラ
イト、パラフィンワックス、モンタンワックス類、キャ
ンデリンワックス、セレシンワックス、マイクロクリス
タリンワックス、ライスワックスなどの天然ワックス、
ポリエチレンワックス、フィッシャートロプシュワック
ス、モンタンワックス誘導体、パラフィンワックス誘導
体、マイクロクリスタリンワックス誘導体、高級脂肪酸
等が挙げられる。これらのなかで融点が50℃〜150
℃の範囲で、140℃における溶融粘度が0.02Pa
/s以下であることが好ましい。画像SN、感度の点で
好ましい。また、JIS K2530−1976に規定
される針入度が1以下であることが耐刷力の点で好まし
い。As waxes, natural waxes such as carnauba wax, beeswax, whale wax, wood wax, jojoba oil, lanolin, ozokerite, paraffin wax, montan wax, candelin wax, ceresin wax, microcrystalline wax and rice wax. ,
Examples thereof include polyethylene wax, Fischer-Tropsch wax, montan wax derivative, paraffin wax derivative, microcrystalline wax derivative, and higher fatty acid. Among these, the melting point is 50 ℃ ~ 150
Melt viscosity at 140 ° C in the range of 0 ° C is 0.02 Pa
/ S or less is preferable. It is preferable in terms of image SN and sensitivity. Further, it is preferable in terms of printing durability that the needle penetration defined by JIS K2530-1976 is 1 or less.
【0045】上記諸特性を満たす熱溶融性物質として
は、カルナバワックス、キャンデリラワックス、FTワ
ックス等が好ましい。Carnauba wax, candelilla wax, FT wax and the like are preferable as the heat-melting substance satisfying the above various characteristics.
【0046】本発明において、画像形成層に含まれる、
熱可塑性もしくは熱溶融性粒子の平均粒径は0.1μm
〜0.5μmであることが好ましい。これらの物性は良
好な耐刷性を得る上で重要である。画像形成層中に含ま
れる親油性を有する熱溶融性粒子の含有量は、40質量
%〜100質量%であることが好ましい。In the present invention, contained in the image forming layer,
The average particle size of the thermoplastic or heat-meltable particles is 0.1 μm
It is preferably 0.5 μm. These physical properties are important for obtaining good printing durability. The content of the lipophilic heat-meltable particles contained in the image forming layer is preferably 40% by mass to 100% by mass.
【0047】本発明においては、第1最表面層が画像形
成層あってもよく、この場合、潤滑性成分が親油性の熱
可塑性もしくは熱溶融性粒子の役割を果たしていても良
い。潤滑性成分でかつ親油性の熱可塑性もしくは熱溶融
性粒子の両方の役割を果たし、画像SNが良好なものと
して、ワックス類、とりわけカルナバワックスが好まし
い。In the present invention, the first outermost surface layer may be an image forming layer, and in this case, the lubricating component may play the role of lipophilic thermoplastic or heat melting particles. Waxes, especially carnauba wax, are preferable as those having both a lubricating component and lipophilic thermoplastic or heat-melting particles and good image SN.
【0048】本発明に係る画像形成層には、室温保存時
の、熱可塑性もしくは熱溶融性粒子の融着防止剤として
水溶性樹脂を含有していても良い。利用可能な水溶性樹
脂としては、水溶性(コ)ポリマー、例えば、合成ホモ
−もしくはコポリマー、例えばポリビニルアルコール、
ポリ(メタ)アクリル酸、ポリ(メタ)アクリルアミ
ド、ポリヒドロキシエチル(メタ)アクリレート、ポリ
ビニルメチルエーテル、又は天然結合剤、例えばゼラチ
ン、多糖類、例えばデキストラン、プルラン、セルロー
ス、アラビアゴム、アルギニン酸、ポリエチレングリコ
ール、ポリエチレンオキサイドなど公知のものが利用で
きるが、未露光部の熱可塑性もしくは熱溶融性粒子の融
着防止を維持しつつ、耐刷性を確保する点でオリゴ糖が
好ましい。オリゴ糖とは数個の単糖がグリコシド結合に
よって脱水縮合したものである。それらのうち本発明に
おいては、トレハロース、マルトース、がラクトース、
スクロースなどが特に好ましい。画像形成層中に含まれ
る水溶性樹脂の含有量は、0質量%〜50質量%である
ことが好ましい。The image-forming layer according to the present invention may contain a water-soluble resin as a fusion preventing agent for thermoplastic or heat-meltable particles during storage at room temperature. Water-soluble resins that can be used include water-soluble (co) polymers such as synthetic homo- or copolymers such as polyvinyl alcohol,
Poly (meth) acrylic acid, poly (meth) acrylamide, polyhydroxyethyl (meth) acrylate, polyvinyl methyl ether, or natural binders such as gelatin, polysaccharides such as dextran, pullulan, cellulose, gum arabic, arginine acid, polyethylene Known compounds such as glycol and polyethylene oxide can be used, but oligosaccharides are preferable in terms of ensuring printing durability while maintaining prevention of fusion of thermoplastic or heat-meltable particles in the unexposed area. Oligosaccharides are dehydrated and condensed from several monosaccharides by glycosidic bonds. Among them, in the present invention, trehalose, maltose, lactose,
Sucrose and the like are particularly preferable. The content of the water-soluble resin contained in the image forming layer is preferably 0% by mass to 50% by mass.
【0049】本発明に係る画像形成層に充分な耐刷力を
付与する観点から、画像形成層の付量は1m2当たり
0.1g〜1.0gの範囲に調整することが好ましい。From the viewpoint of imparting sufficient printing durability to the image forming layer according to the present invention, it is preferable to adjust the amount of the image forming layer to be in the range of 0.1 g to 1.0 g per 1 m 2 .
【0050】《基材》本発明に係る基材について説明す
る。<< Substrate >> The substrate according to the present invention will be described.
【0051】本発明に係る基材としては、プラスチック
基材がロール状に巻き取る工程を円滑に行える点、平版
印刷版材料をロール状で保管し易い点で好ましい。The substrate according to the present invention is preferable in that the step of winding the plastic substrate into a roll can be carried out smoothly and the planographic printing plate material can be easily stored in a roll.
【0052】利用可能なプラスチックとしては、ポリエ
チレンテレフタレート、ポリエチレンナフタレート、ポ
リイミド、ポリアミド、ポリカーボネート、ポリスルホ
ン、ポリフェニレンオキサイド、セルロースエステル類
等が好ましいが、中でも、特にポリエチレンテレフタレ
ート、ポリエチレンナフタレートが好ましく用いられ
る。また、本発明に係る基材には、後述する親水性層も
しくは親水性層の易接着層の接着性を向上させるため
に、コロナ放電処理、プラズマ放電処理を行ってもよ
い。As the usable plastics, polyethylene terephthalate, polyethylene naphthalate, polyimide, polyamide, polycarbonate, polysulfone, polyphenylene oxide, cellulose esters and the like are preferable, and among them, polyethylene terephthalate and polyethylene naphthalate are particularly preferable. Further, the substrate according to the present invention may be subjected to corona discharge treatment or plasma discharge treatment in order to improve the adhesiveness of the hydrophilic layer or the easily-adhesive layer of the hydrophilic layer described later.
【0053】本発明において、基材が画像形成層を有す
る側の第1最表面層とは反対側の第2最表面層であって
もよく、むしろ、バックコート層を設けない方が製造負
荷および低コストの面で好ましい
《親水性層》本発明に係る親水性層について説明する。In the present invention, the base material may be the second outermost surface layer on the side opposite to the first outermost surface layer on the side having the image forming layer. And <hydrophilic layer> which is preferable in terms of low cost The hydrophilic layer according to the present invention will be described.
【0054】本発明においては画像形成層と基材の間に
親水性層を設けることが出来る。本発明の親水性層とし
ては、親水性樹脂や自己造膜可能な微粒子と無機微粒子
より構成されたものが挙げられる。In the present invention, a hydrophilic layer can be provided between the image forming layer and the base material. Examples of the hydrophilic layer of the present invention include those composed of a hydrophilic resin, fine particles capable of self-forming a film, and inorganic fine particles.
【0055】利用可能な親水性樹脂としては、ポリビニ
ルアルコール、アクリル系共重合体、ポリウレタン類、
セルロース誘導体などが挙げられる。ポリビニルアルコ
ールとしてはケン化度が95%以上のものが好ましい。
また、部分的にカルボキシル基で修飾されたものも利用
できる。アクリル系共重合体としては親水性の高い官能
基を有するモノマーを高含有率で合成されたものが利用
でき、親水性の高いモノマーとしてはアクリルアミド、
メチロールアクリルアミド、メチロールメタクリルアミ
ド、アクリル酸、メタクリル酸、ヒドロキシエチルアク
リレート、ヒドロキシエチルメタクリレート、またアン
モニウム、ホスホニウム塩を含有するモノマー、スルホ
ン酸基、ホスホン酸基、リン酸基を含むモノマーが挙げ
られる。As usable hydrophilic resins, polyvinyl alcohol, acrylic copolymers, polyurethanes,
Examples include cellulose derivatives. The polyvinyl alcohol preferably has a saponification degree of 95% or more.
Further, those partially modified with a carboxyl group can also be used. As the acrylic copolymer, those obtained by synthesizing a monomer having a highly hydrophilic functional group at a high content rate can be used, and as the highly hydrophilic monomer, acrylamide,
Examples thereof include methylol acrylamide, methylol methacrylamide, acrylic acid, methacrylic acid, hydroxyethyl acrylate, hydroxyethyl methacrylate, ammonium, a monomer containing a phosphonium salt, a sulfonic acid group, a phosphonic acid group, and a phosphoric acid group-containing monomer.
【0056】ポリマーに共重合したのちそれらの親水性
の官能基を塩にしたものも利用できる。ポリウレタン類
としてはその側鎖にカルボキシル基、リン酸基、スルホ
ン酸基、アミノ基もしくはそれらの塩、水酸基、アミド
基、ポリオキシエチレン基等の親水性官能基を含むもの
が利用できる。セルロース誘導体としてはヒドロキシエ
チルセルロース、カルボキシメチルセルロース、ヒドロ
キシプロピルメチルセルロース、ヒドロキシプロピルセ
ルロースなどが挙げられる。It is also possible to use a salt obtained by polymerizing the hydrophilic functional group of the polymer after copolymerization. As the polyurethanes, those having a hydrophilic functional group such as a carboxyl group, a phosphoric acid group, a sulfonic acid group, an amino group or a salt thereof, a hydroxyl group, an amide group and a polyoxyethylene group in its side chain can be used. Examples of the cellulose derivative include hydroxyethyl cellulose, carboxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxypropyl cellulose and the like.
【0057】利用可能な自己造膜可能な微粒子としては
アルミナゾルやコロイダルシリカが挙げられるが、とり
わけ50nm以下の粒子径を有するコロイダルシリカが
親水性層塗膜強度、親水性確保の点で好ましい。具体的
には日産化学工業(株)製の「スノーテックス」シリー
ズが利用できる。また適度な塗膜強度と保水性を両立す
るためにネックレス状のコロイダルシリカを利用するこ
とも出来る。ネックレス状コロイダルシリカとは1次粒
子径がnmのオーダーである球状シリカの連続体の水分
散系の総称である。ネックレス状のコロイダルシリカと
しては、具体的には日産化学工業(株)製の「スノーテ
ックス−PS」シリーズなどが挙げられる。同シリーズ
のアルカリ性の製品名としては「スノーテックス−PS
−S(連結した状態の平均粒子径は110nm程
度)」、「スノーテックス−PS−M(連結した状態の
平均粒子径は120nm程度)」及び「スノーテックス
−PS−L(連結した状態の平均粒子径は170nm程
度)」があり、これらにそれぞれ対応する酸性の製品が
「スノーテックス−PS−S−O」、「スノーテックス
−PS−M−O」及び「スノーテックス−PS−L−
O」である。Alumina sol and colloidal silica are mentioned as usable self-forming film-forming fine particles, and colloidal silica having a particle diameter of 50 nm or less is particularly preferable from the viewpoint of strength of hydrophilic layer coating and ensuring hydrophilicity. Specifically, the "Snowtex" series manufactured by Nissan Chemical Industries, Ltd. can be used. Necklace-shaped colloidal silica can also be used in order to achieve both appropriate coating strength and water retention. Necklace-shaped colloidal silica is a general term for an aqueous dispersion system of a continuous body of spherical silica having a primary particle diameter of the order of nm. Specific examples of the necklace-shaped colloidal silica include "Snowtex-PS" series manufactured by Nissan Chemical Industries, Ltd. As the alkaline product name of the series, "Snowtex-PS
-S (average particle size of linked state is about 110 nm), "Snowtex-PS-M (average particle size of linked state is about 120 nm)" and "Snowtex-PS-L (average of linked state)" The particle size is about 170 nm) ", and the corresponding acidic products are" Snowtex-PS-SO "," Snowtex-PS-MO "and" Snowtex-PS-L- ".
O ”.
【0058】尚、ここでいう自己造膜とは乾燥膜厚を
1.0μm程度になるように塗布し100℃3分の乾燥
を施した塗膜を作製し、該塗膜を水に10分間浸漬した
のち、スポンジで擦っても塗膜に欠陥が生じないものを
自己造膜したとみなす。The term "self-forming film" as used herein refers to a coating film which is applied so that the dry film thickness is about 1.0 μm and dried at 100 ° C. for 3 minutes, and the coating film is immersed in water for 10 minutes. After immersion, a film that does not cause defects in the coating film even if it is rubbed with a sponge is considered to have undergone self-coating.
【0059】上述の親水性樹脂と自己造膜可能な微粒子
は併用しても良い。親水層に利用可能な無機微粒子とし
ては炭酸カルシウム、硫酸バリウム、シリカ、酸化チタ
ン、クレー、アルミナ等があげられるが、機械的強度向
上と親水性、保水性向上および後述する不感脂化処理が
効果の発揮という点からシリカ、アルミナ、酸化チタ
ン、酸化亜鉛が好ましい。無機粒子の粒径は平均粒径は
0.01μmから10μmであることが好ましく、さら
には0.05μmから5μmであることが好ましい。The hydrophilic resin and the fine particles capable of forming a film may be used in combination. Examples of the inorganic fine particles that can be used in the hydrophilic layer include calcium carbonate, barium sulfate, silica, titanium oxide, clay, alumina, etc., but mechanical strength improvement and hydrophilicity, water retention improvement and desensitizing treatment described later are effective. Silica, alumina, titanium oxide, and zinc oxide are preferable from the viewpoint of exhibiting the above. The average particle size of the inorganic particles is preferably 0.01 μm to 10 μm, and more preferably 0.05 μm to 5 μm.
【0060】前述の親水性樹脂もしくは自己造膜可能な
微粒子と無機微粒子の比率は質量比で2〜50:10〜
50であることが親水性層の機械的強度および保水性の
確保、画像耐久性(以下画像耐刷性と記す)する為の表
面の凹凸を確保する上で好ましい。The above-mentioned hydrophilic resin or fine particles capable of self-forming and the inorganic fine particles have a mass ratio of 2 to 50:10.
It is preferably 50 in order to secure the mechanical strength and water retention of the hydrophilic layer and to secure the surface irregularities for image durability (hereinafter referred to as image printing durability).
【0061】本発明に係る親水性層にはさらなる機械的
強度を確保する目的で、架橋剤を用いて架橋構造を付与
しても良い。架橋剤としてはホルムアルデヒド、エポキ
シ樹脂、メラミン樹脂、グリオキサル、ポリイソシアナ
ート、加水分解テトラアルキルオルトシリケートなどが
利用できる。本発明において、親水性層中における架橋
剤の含有比率は0〜1質量%であることが好ましい。親
水性層の1m2当たりの付量は0.5g〜10gである
ことが好ましく、更に好ましくは、1.0g〜5gであ
る。A cross-linking structure may be imparted to the hydrophilic layer according to the present invention by using a cross-linking agent for the purpose of ensuring further mechanical strength. As the crosslinking agent, formaldehyde, epoxy resin, melamine resin, glyoxal, polyisocyanate, hydrolyzed tetraalkyl orthosilicate, etc. can be used. In the present invention, the content ratio of the crosslinking agent in the hydrophilic layer is preferably 0 to 1% by mass. The coating amount per 1 m 2 of the hydrophilic layer is preferably 0.5 g to 10 g, more preferably 1.0 g to 5 g.
【0062】《光熱変換剤》本発明に係る光熱変換剤に
ついて説明する。<< Photothermal Conversion Agent >> The photothermal conversion agent according to the present invention will be described.
【0063】本発明に係る画像形成層または親水性層中
には、レーザー光を吸収して発熱を生じる光熱変換剤を
使用することができる。In the image forming layer or the hydrophilic layer according to the present invention, a photothermal conversion agent which absorbs laser light and generates heat can be used.
【0064】前記光熱変換剤は効率良く光を吸収し熱に
変換する材料が好ましく、使用する光源によって異なる
が、例えば近赤外光を放出する半導体レーザを光源とし
て使用する場合、近赤外に吸収帯を有する近赤外光吸収
剤が好ましく、例えば、カーボンブラツク、シアニン系
色素、ポリメチン系色素、アズレニウム系色素、スクワ
リリウム系色素、チオピリリウム系色素、ナフトキノン
系色素、アントラキノン系色素等の有機化合物、フタロ
シアニン系、アゾ系、チオアミド系の有機金属錯体、C
o、Cr、Fe、Mn、Ni、Cu、Tiなど金属およ
びそれらの酸化物、窒化物、もしくは酸窒化物などが好
適に用いられる。本発明において画像形成層もしくは親
水性層における光熱変換剤の含有比率は3質量%〜20
質量%であることが好ましい。The photothermal conversion agent is preferably a material that efficiently absorbs light and converts it into heat, and it varies depending on the light source used. For example, when a semiconductor laser emitting near infrared light is used as a light source, Near-infrared light absorber having an absorption band is preferable, for example, carbon black, cyanine dyes, polymethine dyes, azurenium dyes, squarylium dyes, thiopyrylium dyes, naphthoquinone dyes, organic compounds such as anthraquinone dyes, Phthalocyanine-based, azo-based, thioamide-based organometallic complexes, C
Metals such as o, Cr, Fe, Mn, Ni, Cu and Ti and oxides, nitrides or oxynitrides thereof are preferably used. In the present invention, the content ratio of the photothermal conversion agent in the image forming layer or the hydrophilic layer is 3% by mass to 20%.
It is preferably mass%.
【0065】また、光熱変換剤としては、具体的には、
特開昭63−139191号公報、同64−33547
号公報、特開平1−160683号公報、同1−280
750号公報、同1−293342号公報、同2−20
74号公報、同3−26593号公報、同3−3099
1号公報、同3−34891号公報、同3−36093
号公報、同3−36094号公報、同3−36095号
公報、同3−42281号公報、同3−97589号公
報、同3−103476号公報等に記載の化合物が挙げ
られる。これらは1種または、2種以上を組み合わせて
用いることができる。Further, as the photothermal conversion agent, specifically,
JP-A-63-139191 and 64-33547.
No. 1,160,683, and No. 1-280.
750, 1-293342, and 2-20.
No. 74, No. 3-26593, No. 3-3099.
No. 1, JP-A-34891, JP-A No. 3-36093.
Examples thereof include compounds described in JP-A Nos. 3-36094, 3-36095, 3-42281, 3-97589, and 3-103476. These can be used alone or in combination of two or more.
【0066】《平版印刷版材料の製造方法》本発明の平
版印刷版の製造方法について説明する。<< Method for Producing Lithographic Printing Plate Material >> The method for producing the lithographic printing plate of the present invention will be described.
【0067】本発明の平版印刷版材料は公知の塗布方法
を用いて、親水性層、画像形成層、第1最表面を逐次塗
布乾燥することにより作製される。利用可能な塗布方法
としては押し出しコーター塗布、カーテンコーター塗
布、ワイヤーバー塗布、グラビア塗布、スライドコータ
ー塗布等を適用することができる。The lithographic printing plate material of the present invention is produced by sequentially coating and drying the hydrophilic layer, the image forming layer and the first outermost surface using a known coating method. As applicable coating methods, extrusion coater coating, curtain coater coating, wire bar coating, gravure coating, slide coater coating and the like can be applied.
【0068】本発明においては、潤滑性成分を含有する
第1最表層(画像形成層が潤滑性成分を含有する場合は
画像形成層)を塗設した後、平版印刷版材料はロール状
に巻き取られる。巻き取った後に平版印刷版材料として
使用することにより、敢えて、バックコート層などを設
けることなく、搬送ジャムが低減でき、印刷歩留まりが
向上する。In the present invention, the lithographic printing plate material is wound into a roll after coating the first outermost layer containing the lubricating component (or the image forming layer when the image forming layer contains the lubricating component). Taken. By using as a lithographic printing plate material after winding, the conveyance jam can be reduced and the printing yield is improved without intentionally providing a back coat layer or the like.
【0069】本発明において請求項6、7項に記載のよ
うな、第1最表面層や第2最表面層の静止摩擦係数の値
を安定に調整するためには、平版印刷版材料はロール状
に巻き取られた後、製版の直前までロール状を維持して
おくことが好ましい。さらにはロール状に巻き取られた
後、包装材料で包装しておくことが、環境変動にも影響
されず請求項6、7項の関係を安定して得るために好ま
しい。In the present invention, in order to stably adjust the values of the static friction coefficients of the first outermost surface layer and the second outermost surface layer as described in claims 6 and 7, the planographic printing plate material is a roll. After being wound into a shape, it is preferable to maintain the roll shape until immediately before plate making. Furthermore, it is preferable that the material is wound into a roll and then wrapped with a packaging material in order to stably obtain the relationships of claims 6 and 7 without being affected by environmental changes.
【0070】また、ロール状に巻き取る方法であるが、
例えば、製造ライン中で、基材にかかるテンションを5
0kg/mm2〜500kg/mm2の範囲になるように
調整しながらワインダーを用いて巻き取る方法が一例と
して挙げられる。Further, the method of winding in a roll,
For example, in the production line, the tension applied to the substrate is 5
0kg / mm 2 ~500kg / while adjusting to be in the range of mm 2 wound with a winder process as an example.
【0071】包装材料としては水分透過率(JIS K
7129−1992;測定条件は、試験温度40℃、
相対湿度90%RH)が少ないものが好ましく、具体的
には15g/atm・m2・25℃・day以下ものが
好ましい。The moisture permeability (JIS K
7129-1992; measurement conditions are a test temperature of 40 ° C.,
Those having a low relative humidity of 90% RH) are preferable, and specifically, those having a relative humidity of 15 g / atm · m 2 · 25 ° C. · day or less are preferable.
【0072】(包装材料)本発明に用いられる包装材料
としては、ポリエチレン系樹脂、ナイロン系樹脂、ポリ
プロピレン系樹脂、ポリエチレンテレフタレート系樹
脂、ポリアミド系樹脂、エチレン−ビニルアルコール共
重合体系樹脂、エチレン−酢酸ビニル共重合体系樹脂、
アクリロニトリル−ブタジエン共重合体系樹脂、セロハ
ン系樹脂、ビニロン系樹脂、塩化ビニリデン系樹脂およ
びそれらがラミネートなどにより貼合された複合材料が
挙げられる。(Packaging Material) As the packaging material used in the present invention, polyethylene resin, nylon resin, polypropylene resin, polyethylene terephthalate resin, polyamide resin, ethylene-vinyl alcohol copolymer resin, ethylene-acetic acid. Vinyl copolymer resin,
Examples thereof include acrylonitrile-butadiene copolymer resin, cellophane resin, vinylon resin, vinylidene chloride resin, and composite materials obtained by laminating them.
【0073】更には、例えば上記の合成樹脂フィルムの
間にアルミ箔又はアルミ蒸着合成樹脂を使用するなど、
各種ガスバリアー膜を用いても良い。Further, for example, aluminum foil or aluminum vapor-deposited synthetic resin is used between the above synthetic resin films,
Various gas barrier films may be used.
【0074】これらの積層膜又は単一層の膜厚の合計
は、1μm〜3000μm、より好ましくは10μm〜
2000μm、更に好ましくは50μm〜1000μm
であることが好ましい。The total thickness of these laminated films or single layers is 1 μm to 3000 μm, more preferably 10 μm to
2000 μm, more preferably 50 μm to 1000 μm
Is preferred.
【0075】《平版印刷版材料の製版方法》本発明に係
る平版印刷版材料の製版方法を含めた使用方法について
説明する。<< Plate-making method of lithographic printing plate material >> A method of using the lithographic printing plate material according to the present invention including a plate-making method will be described.
【0076】本発明の平版印刷版材料は、一旦、ロール
状に巻き取り、さらに包装材料で包装されている場合に
は製版の事前に包装材料を取り外して、平版印刷版材料
を繰り出し、露光を行う。ロール状に巻き取られた平版
印刷版材料が露光には親水性層もしくは画像形成層に含
有される光熱変換剤の吸収波長に対応したレーザー光源
が利用でき、Arイオンレーザー、Krイオンレーザ
ー、He−Neレーザー、He−Cdレーザー、ルビー
レーザー、ガラスレーザー、チタンサファイヤレーザ
ー、色素レーザー、窒素レーザー、金属蒸気レーザー、
エキシマレーザー、半導体レーザー、YAGレーザーな
どから選択される。The lithographic printing plate material of the present invention is once wound into a roll, and if it is further wrapped with a packaging material, the packaging material is removed before the plate making, and the lithographic printing plate material is unwound and exposed. To do. For exposure of the lithographic printing plate material wound into a roll, a laser light source corresponding to the absorption wavelength of the photothermal conversion agent contained in the hydrophilic layer or the image forming layer can be used, and Ar ion laser, Kr ion laser, He -Ne laser, He-Cd laser, ruby laser, glass laser, titanium sapphire laser, dye laser, nitrogen laser, metal vapor laser,
It is selected from excimer laser, semiconductor laser, YAG laser and the like.
【0077】レーザーの走査方法としては、円筒外面走
査、円筒内面走査、平面走査のいずれの方法も利用でき
る。As the laser scanning method, any of the cylindrical outer surface scanning, the cylindrical inner surface scanning and the flat surface scanning can be used.
【0078】《印刷方法》本発明の印刷方法について説
明する。<< Printing Method >> The printing method of the present invention will be described.
【0079】レーザー露光を行った平版印刷版材料は自
動現像機などの処理機を通すことなく、一般の印刷機版
胴に設置することが出来る。版胴を回転させながら、印
刷機の給水ローラーから湿し水、インクローラーから印
刷インクを供給し、版面上にインク画像を形成させ、製
版を行う。本発明の平版印刷版材料においては先に10
秒ほど湿し水を供給し、ついでインクを供給して製版す
ることが、印刷初期に汚れが生じにくく好ましい。続け
て湿し水、インクを平版印刷材料に供給しながら印刷用
紙を給紙し、印刷を行う。The lithographic printing plate material that has been subjected to laser exposure can be installed in a general printing press plate cylinder without passing through a processor such as an automatic processor. While rotating the plate cylinder, dampening water is supplied from the water supply roller of the printing machine, and printing ink is supplied from the ink roller to form an ink image on the plate surface, thereby performing plate making. In the planographic printing plate material of the invention, 10
It is preferable to supply dampening water for about 2 seconds and then supply ink to make a plate, because stains are less likely to occur at the initial stage of printing. Subsequently, printing paper is fed and printing is performed while supplying dampening water and ink to the planographic printing material.
【0080】また、近年普及しつつあるダイレクトイメ
ージング印刷機を使用し、印刷機上で製版と印刷を連続
して行うことも出来る。Further, it is also possible to use a direct imaging printing machine which has become widespread in recent years and continuously perform plate making and printing on the printing machine.
【0081】ダイレクトイメージング印刷機としては特
開平5−77385号公報に記載されたものが利用でき
る。この場合には平版印刷版材料をロール状態から繰り
出して、版胴に適応したサイズにカットした後、版胴に
設置する。As the direct imaging printing machine, the one described in JP-A-5-77385 can be used. In this case, the planographic printing plate material is unrolled from the roll state, cut into a size suitable for the plate cylinder, and then placed on the plate cylinder.
【0082】また、特開平10−272756号公報、
特開2002−225411号公報、同2002−30
7852号公報に記載の印刷機も使用でき、この場合に
は、平版印刷版材料をロール状のまま印刷機に設置がで
きる。Further, Japanese Patent Laid-Open No. 10-272756,
JP-A-2002-225411, 2002-30
The printing machine described in Japanese Patent No. 7852 can be used, and in this case, the planographic printing plate material can be installed in the printing machine in a roll form.
【0083】[0083]
【実施例】以下、実施例により本発明を説明するが、本
発明はこれらに限定されない。EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited thereto.
【0084】実施例1
《平版印刷版材料の製造》下記に記載の方法に従い、平
版印刷版材料を製造した。Example 1 << Production of planographic printing plate material >> A planographic printing plate material was produced according to the method described below.
【0085】《下引き層の塗設》188μm厚、長さ1
000mのPET基材にコロナ放電処理をした後、以下
の組成の第1下塗り層塗布液を20℃、55%RHの雰
囲気下でワイヤーバーにより乾燥後の膜厚が0.4μm
となるように塗布した。その後、15mの長さの140
℃に設定された乾燥ゾーンを搬送スピード15m/分の
速度で通過させ、第1下塗り層を塗設した。<< Coating of undercoat layer >> 188 μm thick, length 1
After performing a corona discharge treatment on a PET base material of 000 m, the first undercoat layer coating liquid having the following composition has a film thickness of 0.4 μm after drying with a wire bar in an atmosphere of 20 ° C. and 55% RH.
Was applied so that After that, 140 of 15m in length
The first undercoat layer was applied by passing through a drying zone set at ° C at a conveying speed of 15 m / min.
【0086】次いで、第1下塗り層を塗設した面に、コ
ロナ放電処理を施した後、下記の第2下塗り層塗布液
を、35℃、22%RHの雰囲気下でエアーナイフ方式
により乾燥後の膜厚が0.1μmとなるように塗布し
た。Then, after corona discharge treatment was applied to the surface coated with the first undercoat layer, the following second undercoat layer coating solution was dried by an air knife method in an atmosphere of 35 ° C. and 22% RH. Was applied to give a film thickness of 0.1 μm.
【0087】その後、15mの長さの140℃に設定さ
れた乾燥ゾーンを搬送スピード15m/分の速度で通過
させ、第2下塗り層を塗設し、第1下塗り層と第2下塗
り層からなる下引き層を形成した。Then, a drying zone having a length of 15 m and set at 140 ° C. is passed at a conveying speed of 15 m / min to apply a second undercoat layer, which is composed of a first undercoat layer and a second undercoat layer. An undercoat layer was formed.
【0088】
(第1下塗り層塗布液の組成)
アクリルラテックス粒子(n−BA/tert−BA/St/HEMA)
=(28/22/25/25) 36.9質量部
界面活性剤(A) 0.36質量部
硬膜剤(a) 0.98質量部
上記素材に蒸留水を加えて1000mlとし、第1下塗
り層塗布液とした。また、上記アクリルラテックス粒子
の形成に用いた、各単量体を下記に示す。(Composition of coating liquid for first undercoat layer) Acrylic latex particles (n-BA / tert-BA / St / HEMA) = (28/22/25/25) 36.9 parts by mass Surfactant (A) 0.36 parts by mass Hardener (a) 0.98 parts by mass Distilled water was added to the above material to make 1000 ml, to give a first undercoat layer coating liquid. In addition, each monomer used for forming the acrylic latex particles is shown below.
【0089】
n−BA :n−ブチルアクリレート
tert−BA:tert−ブチルアクリレート
St :スチレン
HEMA :ヒドロキシエチルメタクリレート
(第2下塗り層塗布液の組成)
ゼラチン 9.6質量部
界面活性剤(A) 0.4質量部
硬膜剤(b) 0.1質量部
上記素材に蒸留水を加えて1000mlとし、第2下塗
り層塗布液とした。N-BA: n-butyl acrylate tert-BA: tert-butyl acrylate St: styrene HEMA: hydroxyethyl methacrylate (composition of the second undercoat layer coating solution) gelatin 9.6 parts by mass Surfactant (A) 0 0.4 parts by mass Hardener (b) 0.1 parts by mass Distilled water was added to the above material to make 1000 ml, to obtain a second undercoat layer coating solution.
【0090】[0090]
【化1】 [Chemical 1]
【0091】《親水性層の塗設》下引き層が付与された
PET基材上に、下記の親水性層塗布液をワイヤバー#
5を用いて塗布し、15mの長さの100℃に設定され
た乾燥ゾーンを搬送スピード15m/分の速度で通過さ
せた。塗布後、巻き取られたロールはさらに、60℃で
24時間の熱処理を施した。なお、親水性層の付量は
2.0g/m2であった。<< Coating of Hydrophilic Layer >> On a PET substrate provided with an undercoat layer, the following hydrophilic layer coating solution was applied to a wire bar #
No. 5 was applied, and a drying zone set at 100 ° C. having a length of 15 m was passed at a conveying speed of 15 m / min. After coating, the wound roll was further subjected to heat treatment at 60 ° C. for 24 hours. The coating amount of the hydrophilic layer was 2.0 g / m 2 .
【0092】(親水性層塗布液の調製)予め、以下の
(a)、(b)及び(c)を混合した固形分30%の水
分散液を調製しておく。(Preparation of Hydrophilic Layer Coating Liquid) An aqueous dispersion having a solid content of 30% is prepared in advance by mixing the following (a), (b) and (c).
【0093】
(a)コロイダルシリカ(スノーテックスS、固形分30%;
日産化学工業社製) 17.34質量部
(b)コロイダルシリカ(スノーテックスPS−M、固形分20%;
日産化学工業社製) 38.89質量部
(c)アルミノシリケート粒子(AMTシリカ08、粒径0.6μm;
水澤化学工業社製) 4.50質量部
上記記載の(a)、(b)及び(c)を含む固形分30
%の水分散液に下記の素材を混合して、ホモジナイザー
で1時間分散し、親水性層塗布液を調製した。(A) Colloidal silica (Snowtex S, solid content 30%; manufactured by Nissan Chemical Industries, Ltd.) 17.34 parts by mass (b) Colloidal silica (Snowtex PS-M, solid content 20%; Nissan Chemical Industries, Ltd.) 38.89 parts by mass (c) Aluminosilicate particles (AMT silica 08, particle size 0.6 μm; manufactured by Mizusawa Chemical Industry Co., Ltd.) 4.50 parts by mass The above-mentioned (a), (b) and (c) Solid content including 30
% Of the aqueous dispersion, the following materials were mixed and dispersed for 1 hour with a homogenizer to prepare a hydrophilic layer coating solution.
【0094】
カルボキシメチルセルロースのナトリウム塩(4%水溶液)
(関東化学社製) 5.00質量部
Fe、Mn、Cuの複合酸化物(MFブラック4500、
40%水分散液;大日精化工業社製) 4.50質量部
モンモリロナイト(ベンゲル31;豊順洋行)の5%水溶液
8.00質量部
シリコン系界面活性剤(FZ2161;日本ユニカー社製)
の1%水溶液 2.27質量部
Na3PO4(関東化学社製)の10%水溶液 1.00質量部
純水 18.69質量部
《画像形成層の塗布と平版印刷版材料1〜4の製造》上
記で形成した親水性層上に下記組成の画像形成層塗布液
1〜4をワイヤバー#5を用いて塗布し、15mの長さ
の60℃に設定された乾燥ゾーンを搬送スピード15m
/分の速度で通過させ、画像形成層を形成した。なお、
いずれの画像形成層も塗布付量は0.5g/m2であっ
た。Sodium salt of carboxymethyl cellulose (4% aqueous solution) (manufactured by Kanto Chemical Co., Inc.) 5.00 parts by mass Fe, Mn, Cu complex oxide (MF black 4500, 40% aqueous dispersion; manufactured by Dainichi Seika Kogyo Co., Ltd.) ) 4.50 parts by mass 5% aqueous solution of montmorillonite (Bengel 31; Toyojun Yoko) 8.00 parts by mass 1% aqueous solution of silicon-based surfactant (FZ2161; manufactured by Nippon Unicar Co., Ltd.) 2.27 parts by mass Na 3 PO 4 (Kanto Chemical Co., Inc.) 10% aqueous solution 1.00 parts by weight Pure water 18.69 parts by weight << Application of image forming layer and production of planographic printing plate materials 1 to 4 >> The following composition was formed on the hydrophilic layer formed above. Coating solutions 1 to 4 for the image forming layer are applied using a wire bar # 5, and a drying zone having a length of 15 m and set at 60 ° C. is conveyed at a conveying speed of 15 m.
The image forming layer was formed by passing at a speed of 1 / min. In addition,
The coating amount of each of the image forming layers was 0.5 g / m 2 .
【0095】画像形成層の塗設後、ロール状に巻き取ら
れた試料を50℃で24時間の熱処理を施し、第1最表
面層が画像形成層である平版印刷版材料1〜4を各々製
造した。After coating the image forming layer, the sample wound into a roll was subjected to heat treatment at 50 ° C. for 24 hours, and each of the lithographic printing plate materials 1 to 4 having the image forming layer as the first outermost layer was processed. Manufactured.
【0096】
(画像形成層塗布液1;親油性で粒子形状の潤滑性成分としてカルナバワック
ス粒子を含有している)
カルナバワックス粒子水分散液(Hi−Disper A−118、
平均粒径0.5μm、固形分40%;岐阜セラック製造所社製)
7.50質量部
トレハロース(トレハ;林原商事製) 2.00質量部
純水 90.50質量部
(画像形成層塗布液2;親油性で粒子形状の潤滑性成分としてカルナバワック
ス粒子を含有している)
カルナバワックス粒子水分散液(Hi−Disper A−118、
平均粒径0.5μm、固形分40%;岐阜セラック製造所社製)
3.50質量部
スチレンアクリルラテックス(ヨドゾールGD87B、平均粒径
0.09μm、固形分48%;日本NSC社製) 3.00質量部
トレハロース(トレハ;林原商事製) 2.00質量部
純水 90.50質量部
(画像形成層塗布液3;潤滑性成分としてシリコーンオイルを含有している)
スチレンアクリルラテックス(ヨドゾールGD87B、平均粒径
0.09μm、固形分48%;日本NSC社製) 7.00質量部
シリコーンオイル(TSM631、東芝シリコーン製) 0.50質量部
トレハロース(トレハ;林原商事製) 2.00質量部
純水 90.50質量部
(画像形成層塗布液4;潤滑性成分を含有していない)
スチレンアクリルラテックス(ヨドゾールGD87B、平均粒径
0.09μm、固形分48%;日本NSC社製) 7.40質量部
トレハロース(トレハ;林原商事製) 2.00質量部
純水 90.50質量部
《平版印刷版材料5の製造》:ロール状
平版印刷版材料1の製造において、画像形成層の塗設
後、ロール状に巻き取られた試料を50℃で24時間の
熱処理を施した後、パルプ/アルミ箔/ポリエチレン樹
脂がラミネートにより貼合された包装材料{水分透過率
(JIS K 7129−1992;測定条件は、試験
温度40℃、相対湿度90%RH)は7g/atm・m
2・25℃・day}で包装し、平版印刷版材料5を得
た。(Image Forming Layer Coating Liquid 1; Lipophilic and Containing Carnauba Wax Particles as Lubricating Components in Particle Form) Carnauba wax particle aqueous dispersion (Hi-Disper A-118, average particle size 0.5 μm) , Solid content 40%; manufactured by Gifu Shellac Co., Ltd.) 7.50 parts by mass Trehalose (treha; manufactured by Hayashibara Shoji) 2.00 parts by mass Pure water 90.50 parts by mass (image forming layer coating solution 2; lipophilic and particles) Carnauba wax particles are contained as a lubricity component of shape) Carnauba wax particle water dispersion (Hi-Disper A-118, average particle size 0.5 μm, solid content 40%; manufactured by Gifu Shellac Manufacturing Co., Ltd.) 3. 50 parts by mass Styrene acrylic latex (Iodosol GD87B, average particle size 0.09 μm, solid content 48%; manufactured by NSC Japan Ltd.) 3.00 parts by mass trehalose Treha; manufactured by Hayashibara Shoji Co., Ltd. 2.00 parts by mass Pure water 90.50 parts by mass (Image forming layer coating liquid 3; containing silicone oil as a lubricating component) Styrene acrylic latex (Iodosol GD87B, average particle size: 09 μm, solid content 48%; manufactured by Japan NSC Co., Ltd. 7.00 parts by mass Silicone oil (TSM631, manufactured by Toshiba Silicone) 0.50 parts by mass Trehalose (Treha; manufactured by Hayashibara Shoji) 2.00 parts by mass Pure water 90.50 parts by mass Parts (image forming layer coating solution 4; containing no lubricating component) Styrene acrylic latex (Iodozol GD87B, average particle size 0.09 μm, solid content 48%; manufactured by NSC Japan) 7.40 parts by mass Trehalose (trehah Manufactured by Hayashibara Shoji) 2.00 parts by mass pure water 90.50 parts by mass << Production of planographic printing plate material 5 >>: roll-shaped planographic printing plate In the production of Material 1, after coating the image forming layer, the sample wound into a roll is subjected to heat treatment at 50 ° C. for 24 hours, and then a package in which pulp / aluminum foil / polyethylene resin is laminated by lamination. Material {moisture permeability (JIS K 7129-1992; measurement conditions: test temperature 40 ° C., relative humidity 90% RH): 7 g / atm · m
It was packaged at 2.25 ° C. · day} to obtain a planographic printing plate material 5.
【0097】《平版印刷版材料6の製造》:シート状
平版印刷版材料1の製造において、画像形成層塗布液1
を塗布乾燥した後、ロール状に巻き取ることなくシート
状にカットし、50℃で24時間の熱処理を施し、第1
最表面層が画像形成層である平版印刷版材料6を得た。<< Production of planographic printing plate material 6 >>: In the production of sheet-shaped planographic printing plate material 1, coating liquid 1 for image forming layer
After coating and drying, the product was cut into a sheet without being wound into a roll and subjected to heat treatment at 50 ° C for 24 hours.
A planographic printing plate material 6 having an image forming layer as the outermost surface layer was obtained.
【0098】上記で得られた平版印刷版材料1〜6は、
更に各々25℃、50%RHの環境下に一日安置した各
試料、及び、35℃、80%RHの環境下に1日安置し
た各試料の各々について、以下の評価を行った。The lithographic printing plate materials 1 to 6 obtained above are
Further, the following evaluation was performed on each of the samples that were placed in the environment of 25 ° C. and 50% RH for one day and each of the samples that were placed in the environment of 35 ° C. and 80% RH for one day.
【0099】《潤滑性成分の移行有無の評価》平版印刷
版材料1〜6の画像形成層が塗設されている面(第1最
表面層)とは反対側の面(第2最表面層)を透過型電子
顕微鏡(TEM、倍率10,000倍)で確認し、潤滑
性成分が移行しているか確認し、結果を表1に示す。<< Evaluation of Presence or Absence of Transfer of Lubricating Component >> The surface of the lithographic printing plate materials 1 to 6 opposite to the surface (first outermost surface layer) coated with the image forming layer (second outermost surface layer). ) Is confirmed by a transmission electron microscope (TEM, magnification: 10,000 times), and it is confirmed whether the lubricating component is transferred. The results are shown in Table 1.
【0100】《第1最表面層、第2最表面層の静止摩擦
係数測定》上記の平版印刷版材料1〜6の各々につい
て、画像形成層側が塗設されている面(第1最表面層)
および反対側の面(第2最表面層)の巻き取り前の静止
摩擦係数、巻き取り後の静止摩擦係数を測定した。<< Measurement of Static Friction Coefficients of First Outermost Layer and Second Outermost Layer >> For each of the planographic printing plate materials 1 to 6 described above, the surface coated with the image forming layer side (first outermost surface layer). )
The coefficient of static friction before winding and the coefficient of static friction after winding on the opposite surface (second outermost surface layer) were measured.
【0101】表1には、25℃、65%RHにおける、
巻き取り前、巻き取り後の静止摩擦係数の値を示し、表
2には、35℃、80%RHにおける、巻き取り前、巻
き取り後の静止摩擦係数の値を各々、記載した。Table 1 shows that at 25 ° C. and 65% RH,
The values of the static friction coefficient before and after winding are shown. In Table 2, the values of the static friction coefficient before and after winding at 35 ° C. and 80% RH are shown.
【0102】また、静止摩擦係数の測定は、JIS K
7125に規定された摩擦係数試験方法に準じて行っ
た。The static friction coefficient is measured according to JIS K.
The test was performed according to the friction coefficient test method specified in 7125.
【0103】《搬送性の評価》:搬送ジャムの発生回数
をカウント
特開平10−272756号公報に記載の印刷装置の画
像記録装置25として、半導体レーザー(発光波長83
0nm、レーザーパワー)を導入した印刷装置を用い
(図1参照)、搬送性の評価を行った。<< Evaluation of Transportability >>: Counting Number of Occurrences of Transport Jam As the image recording device 25 of the printing device described in Japanese Patent Laid-Open No. 10-272756, a semiconductor laser (emission wavelength
The transportability was evaluated using a printing apparatus in which 0 nm, laser power) was introduced (see FIG. 1).
【0104】この印刷装置における給版方法であるが、
まず平版印刷版材料を給版機構23に設置する。設置さ
れた平版印刷版材料はガイドロール53、ガイドレール
55を通って版胴に繰り出される。平版印刷版材料は所
望の長さになるようにカッター54で断裁された後、版
胴に巻きつけられる。送られた平版印刷版材料は版抑え
ロール62により版胴に密着させながら版胴に巻き付け
られる。The plate feeding method in this printing apparatus is as follows:
First, the planographic printing plate material is set on the plate feeding mechanism 23. The installed lithographic printing plate material is fed to the plate cylinder through the guide roll 53 and the guide rail 55. The planographic printing plate material is cut by a cutter 54 so as to have a desired length and then wound around the plate cylinder. The sent planographic printing plate material is wound around the plate cylinder while being brought into close contact with the plate cylinder by the plate pressing roll 62.
【0105】この操作のなかでジャムが発生するかを1
0回繰り返し、搬送ジャムが生じた回数をカウントす
る。Check whether jam occurs during this operation.
Repeat 0 times to count the number of times a conveyance jam has occurred.
【0106】この評価をそれぞれ25℃、65%RHお
よび35℃、80%RHの環境下に1日安置した平版印
刷版材料1〜6(平版印刷版材料6の給版についてはガ
イドロール53にくわえさせてから版胴に繰り出した)
について行った。This evaluation was carried out by lithographic printing plate materials 1 to 6 which had been placed in the environment of 25 ° C., 65% RH and 35 ° C., 80% RH for 1 day (for the plate feeding of the lithographic printing plate material 6, the guide roll 53 was used. I let it out and rolled it out to the plate cylinder.)
I went about.
【0107】《印刷評価》ガイドロール53および55
を通って版胴に巻き付けられた平版印刷材料を画像記録
装置25(半導体レーザー)によって250mJ/cm
2のエネルギーで30%平網画像を版面全面に露光す
る。露光後、平版印刷版材料は現像処理を施されること
なく、印刷部位に移動させられる。<< Print Evaluation >> Guide rolls 53 and 55
The lithographic printing material wound around the plate cylinder through the image recording device 25 (semiconductor laser) is set to 250 mJ / cm.
A 30% flat screen image is exposed on the entire plate surface with energy of 2 . After exposure, the lithographic printing plate material is moved to the printing site without being subjected to a development treatment.
【0108】版胴を回転しながら湿し水供給装置22よ
り、アストロマーク3(日研化学研究所製)の2%水溶
液を10秒間供給し、次いでインキ供給装置10よりハ
イエコーM(墨)(東洋インキ製造製)を供給し、紙送
りをすることにより印刷を行った。得られた印刷物上の
キズ汚れ(ガイドローラー53およびガイドレール55
と平版印刷版材料との摺動により発生したものと思われ
る)の個数をカウントする。While the plate cylinder is rotating, a 2% aqueous solution of Astromark 3 (manufactured by Nikken Chemical Laboratory) is supplied from the dampening water supply device 22 for 10 seconds, and then the high echo M (black ink) (ink) is supplied from the ink supply device 10. Toyo Ink Mfg. Co., Ltd.) was supplied and paper was fed to perform printing. Scratches on the obtained printed matter (guide roller 53 and guide rail 55
It is thought that this is caused by the sliding of the lithographic printing plate material and the).
【0109】上記によって得られた結果を表1、表2に
示す。The results obtained as described above are shown in Tables 1 and 2.
【0110】[0110]
【表1】 [Table 1]
【0111】[0111]
【表2】 [Table 2]
【0112】表1及び表2から、比較の試料に比べ、第
1最表面層に潤滑性成分を含有し、とりわけ潤滑性成分
が粒子形状をしており、その製造プロセスにおいてロー
ル状に巻き取る工程を経た(ロール状に巻き取る工程を
製造時の履歴として有するともいう)平版印刷版材料
は、保存環境下の変動によらず搬送ジャムの発送回数、
印刷物上のキズ汚れの頻度が少ないことが明らかであ
る。From Table 1 and Table 2, as compared with the comparative sample, the first outermost surface layer contains a lubricating component, and in particular, the lubricating component has a particle shape, and is wound into a roll in its manufacturing process. The lithographic printing plate material that has undergone the steps (also referred to as having a step of winding into a roll as a history at the time of manufacturing) does not depend on fluctuations in the storage environment,
It is clear that the frequency of scratches on printed matter is low.
【0113】更に、その製造プロセスにおいて包装材料
で包装されたものは保存環境下の変動によらず、全く搬
送ジャムやキズ汚れが発生しないことが確認された。Further, it was confirmed that, in the manufacturing process, the product packaged with the packaging material did not cause any conveyance jam or scratch stain regardless of the change in the storage environment.
【0114】[0114]
【発明の効果】本発明により、搬送時の搬送キズや搬送
不良がなく、画像欠陥が少なく、低コストの平版印刷版
材料とその製造方法を提供し、かつ、前記平版印刷版材
料を用いる印刷方法を提供することことが出来た。According to the present invention, there are provided a lithographic printing plate material which is free from transport scratches and transport defects during transportation, has few image defects, and is low in cost, and a method for producing the same, and printing using the lithographic printing plate material. I was able to provide a method.
【図1】本発明の印刷方法に用いられる印刷装置の一態
様を示す構成図である。FIG. 1 is a configuration diagram showing an aspect of a printing apparatus used in a printing method of the present invention.
11 第1の版胴 12 第2の版胴 13 第1のブランケット胴 14 第2のブランケット胴 15 圧胴 16 給紙胴 17 排紙胴 20 インキ供給装置 21 湿し水供給装置 22 湿し水供給装置 23 給版部 24 排版部 25 画像記録装置 26 現像処理装置 27 給紙部 28 排紙部 31 第1の版胴移動機構 32 第2の版胴移動機構 33 軸受 35 溝孔 36 支軸 38 スライドホルダ 39 モータ 41 ボールネジ 57 くわえ爪 215 版胴 P 印刷版 S 印刷用紙 11 First plate cylinder 12 Second plate cylinder 13 First Blanket Body 14 Second Blanket Body 15 impression cylinder 16 Paper feed cylinder 17 Output cylinder 20 Ink supply device 21 Dampening water supply system 22 Damping water supply device 23 Plate Supply Department 24 Plate ejection section 25 Image recording device 26 Development Processing Equipment 27 Paper feeder 28 Paper output section 31 First plate cylinder moving mechanism 32 Second plate cylinder moving mechanism 33 bearings 35 slots 36 spindle 38 Slide holder 39 motor 41 ball screw 57 grippers 215 plate cylinder P printing plate S printing paper
Claims (13)
る平版印刷版材料の製造方法において、 該基材上に該画像形成層を有する側の第1最表面層が潤
滑性成分を含有するように調整する工程、ロール状に巻
き取る工程とを順次含むことを特徴とする平版印刷版材
料の製造方法。1. A method for producing a lithographic printing plate material having at least an image forming layer on a substrate, wherein the first outermost surface layer on the side having the image forming layer on the substrate contains a lubricating component. The method for producing a lithographic printing plate material, comprising the steps of:
材料で包装される工程を含むことを特徴とする請求項1
に記載の平版印刷版材料の製造方法。2. A step of wrapping with a wrapping material after the step of winding into a roll is included.
The method for producing a lithographic printing plate material as described in.
とを特徴とする請求項1または2に記載の平版印刷版材
料の製造方法。3. The method for producing a lithographic printing plate material according to claim 1, wherein the lithographic printing plate material is in a roll shape.
る平版印刷版材料において、 該基材に該画像形成層を有する側の第1最表面層が潤滑
性成分を含有するように調整する工程、次いで、ロール
状に巻き取る工程を経て製造されたことを特徴とする平
版印刷版材料。4. A lithographic printing plate material having at least an image forming layer on a base material, wherein the first outermost surface layer on the side having the image forming layer on the base material is adjusted to contain a lubricating component. A planographic printing plate material, which is manufactured through a process and a roll-up process.
材料で包装される工程を経て製造されたことを特徴とす
る請求項4に記載の平版印刷版材料。5. The lithographic printing plate material according to claim 4, wherein the lithographic printing plate material is manufactured through a step of packaging with a packaging material after the step of winding into a roll.
特徴とする請求項4または5に記載の平版印刷版材料。6. The lithographic printing plate material according to claim 4, wherein the lubricating component is in the form of particles.
前記潤滑性成分が親油性の熱可塑性もしくは熱溶融性粒
子であることを特徴とする請求項4〜6のいずれか1項
に記載の平版印刷版材料。7. The first outermost layer is an image forming layer,
The lithographic printing plate material according to any one of claims 4 to 6, wherein the lubricating component is a lipophilic thermoplastic or heat-meltable particle.
けられていることを特徴とする請求項4〜7のいずれか
1項に記載の平版印刷版材料。8. The lithographic printing plate material according to claim 4, wherein a hydrophilic layer is provided between the substrate and the image forming layer.
とする請求項4〜8のいずれか1項に記載の平版印刷版
材料。9. The lithographic printing plate material according to claim 4, wherein the base material is made of plastic.
記第1最表面層の静止摩擦係数が0.05以上2.0未
満であり、ロール状に巻き取る工程後の前記第1最表面
層とは反対側の第2最表面層の静止摩擦係数が共に0.
05以上2.0未満であることを特徴とする請求項4〜
9のいずれか1項に記載の平版印刷版材料。10. The first outermost surface layer has a coefficient of static friction of 0.05 or more and less than 2.0 before the step of winding into a roll, and the first outermost layer after the step of winding into a roll. Has a coefficient of static friction of 0.
It is 05 or more and less than 2.0.
10. The lithographic printing plate material as described in any one of 9 above.
記第1最表面層の静止摩擦係数が0.05以上2.0未
満、前記第2最表面層の静止摩擦係数が2.0以上5.
0以下であり、且つ、ロール状に巻き取る工程後の前記
第1最表面層および前記第2最表面層の静止摩擦係数が
共に0.05以上2.0未満であることを特徴とする請
求項10に記載の平版印刷版材料。11. The coefficient of static friction of the first outermost surface layer before the step of winding into a roll is 0.05 or more and less than 2.0, and the coefficient of static friction of the second outermost surface layer is 2.0 or more and 5.
It is 0 or less, and the static friction coefficients of the first outermost surface layer and the second outermost surface layer after the step of winding into a roll are both 0.05 or more and less than 2.0. Item 10. The planographic printing plate material according to Item 10.
請求項4〜11のいずれか1項に記載の平版印刷版材
料。12. The lithographic printing plate material as claimed in claim 4, which has a roll shape.
製造方法により製造された平版印刷版材料Aもしくは、
請求項4〜12のいずれか1項に記載の平版印刷版材料
Bに、レーザー光により画像記録を行う工程、次いで、
該画像記録が行われた該平版印刷版材料Aまたは該平版
印刷版材料Bに、湿し水およびインクを供給して前記平
版印刷版材料A上または前記平版印刷版材料B上にイン
ク画像を形成する工程、形成された該インク画像をシー
ト状の基材に転写する工程を含むことを特徴とする印刷
方法。13. A lithographic printing plate material A manufactured by the manufacturing method according to claim 1, or
A step of recording an image on the lithographic printing plate material B according to any one of claims 4 to 12 with a laser beam,
A fountain solution and ink are supplied to the planographic printing plate material A or the planographic printing plate material B on which the image recording is performed to form an ink image on the planographic printing plate material A or the planographic printing plate material B. A printing method comprising a step of forming and a step of transferring the formed ink image to a sheet-shaped substrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003025668A JP2003300388A (en) | 2002-02-06 | 2003-02-03 | Lithographic printing plate material, method for manufacture thereof, and printing method |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002029200 | 2002-02-06 | ||
JP2002-29200 | 2002-02-06 | ||
JP2003025668A JP2003300388A (en) | 2002-02-06 | 2003-02-03 | Lithographic printing plate material, method for manufacture thereof, and printing method |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2003300388A true JP2003300388A (en) | 2003-10-21 |
Family
ID=29404871
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2003025668A Pending JP2003300388A (en) | 2002-02-06 | 2003-02-03 | Lithographic printing plate material, method for manufacture thereof, and printing method |
Country Status (1)
Country | Link |
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JP (1) | JP2003300388A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010035354A1 (en) | 2008-09-25 | 2010-04-01 | 大日本印刷株式会社 | Thermal transfer sheet |
JP2013159377A (en) * | 2012-02-07 | 2013-08-19 | Toray Ind Inc | Packing method and package of laminate film roll, and method for manufacturing laminate using the laminate film roll |
-
2003
- 2003-02-03 JP JP2003025668A patent/JP2003300388A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010035354A1 (en) | 2008-09-25 | 2010-04-01 | 大日本印刷株式会社 | Thermal transfer sheet |
JP2013159377A (en) * | 2012-02-07 | 2013-08-19 | Toray Ind Inc | Packing method and package of laminate film roll, and method for manufacturing laminate using the laminate film roll |
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