JPS63226658A - Planographic printing material for back exposure - Google Patents
Planographic printing material for back exposureInfo
- Publication number
- JPS63226658A JPS63226658A JP6148087A JP6148087A JPS63226658A JP S63226658 A JPS63226658 A JP S63226658A JP 6148087 A JP6148087 A JP 6148087A JP 6148087 A JP6148087 A JP 6148087A JP S63226658 A JPS63226658 A JP S63226658A
- Authority
- JP
- Japan
- Prior art keywords
- antihalation
- layer
- fine line
- matting agent
- agent
- 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.)
- Granted
Links
- 238000007639 printing Methods 0.000 title claims abstract description 63
- 239000000463 material Substances 0.000 title claims abstract description 30
- 239000006224 matting agent Substances 0.000 claims abstract description 15
- 229910052709 silver Inorganic materials 0.000 claims abstract description 13
- 239000004332 silver Substances 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 230000005540 biological transmission Effects 0.000 claims abstract description 3
- -1 silver halide Chemical class 0.000 claims description 13
- 238000011161 development Methods 0.000 claims description 9
- 239000000839 emulsion Substances 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 5
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract description 7
- 230000003287 optical effect Effects 0.000 abstract description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 6
- 239000011230 binding agent Substances 0.000 abstract description 5
- 239000006229 carbon black Substances 0.000 abstract description 4
- 239000011247 coating layer Substances 0.000 abstract description 4
- 238000009792 diffusion process Methods 0.000 abstract description 3
- 150000003839 salts Chemical class 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 36
- 238000000034 method Methods 0.000 description 26
- 206010016807 Fluid retention Diseases 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000000084 colloidal system Substances 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 4
- 108010010803 Gelatin Proteins 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 239000012792 core layer Substances 0.000 description 2
- 239000011162 core material Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- LUMLZKVIXLWTCI-NSCUHMNNSA-N (e)-2,3-dichloro-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(/Cl)C=O LUMLZKVIXLWTCI-NSCUHMNNSA-N 0.000 description 1
- GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical class CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229920001612 Hydroxyethyl starch Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- SMEWQUCKUGPMKH-UHFFFAOYSA-H [Ti+4].[Ba+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O Chemical compound [Ti+4].[Ba+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O SMEWQUCKUGPMKH-UHFFFAOYSA-H 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- RLDQYSHDFVSAPL-UHFFFAOYSA-L calcium;dithiocyanate Chemical compound [Ca+2].[S-]C#N.[S-]C#N RLDQYSHDFVSAPL-UHFFFAOYSA-L 0.000 description 1
- 239000001913 cellulose Chemical class 0.000 description 1
- 229920002678 cellulose Chemical class 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000000586 desensitisation Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940050526 hydroxyethylstarch Drugs 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
- 239000011133 lead Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 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
- 239000003607 modifier Substances 0.000 description 1
- ZAKLKBFCSHJIRI-UHFFFAOYSA-N mucochloric acid Natural products OC1OC(=O)C(Cl)=C1Cl ZAKLKBFCSHJIRI-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 150000004010 onium ions Chemical class 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229940005642 polystyrene sulfonic acid Drugs 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- RONWGALEIBILOG-VMJVVOMYSA-N quinine sulfate Chemical compound [H+].[H+].[O-]S([O-])(=O)=O.C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21.C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 RONWGALEIBILOG-VMJVVOMYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 1
- 229940103494 thiosalicylic acid Drugs 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(A) 産業上の利用分野
本発明は銀錯塩拡散転写法(DTR法)を利用した平版
印刷材料に関する。DETAILED DESCRIPTION OF THE INVENTION (A) Industrial Field of Application The present invention relates to a lithographic printing material using a silver complex diffusion transfer method (DTR method).
(B) 従来技術及びその問題点
DTR法を利用した平版印刷材料、詳しくは、支持体上
に少なくとも一層の感光層とその上に該感光層に感光記
録された像を反転、転写記録すべき物理現像核の層とか
ら成る材料を画像状に無光後、銀拡散転写現像処理を行
い、核材料の外部表面上に金属銀画像を形成せしめるこ
とにより得られる平版印刷材料は、ダイレクト製版法と
呼ばれ、リスフィルムを中間プロセスとして使用するこ
とに特徴付けられる従来の平版印刷材料(ps版)に較
べ、簡便さ、及び迅速性という利点を有している。(B) Prior art and its problems Planographic printing materials using the DTR method, specifically, at least one photosensitive layer on a support and an image photosensitively recorded on the photosensitive layer on the support should be inverted and transfer-recorded. A lithographic printing material obtained by image-freeing a material consisting of a layer of physical development nuclei and then subjecting it to a silver diffusion transfer development process to form a metallic silver image on the outer surface of the core material can be obtained using the direct plate making method. It has the advantages of simplicity and speed compared to conventional lithographic printing materials (PS plates), which are characterized by the use of lithographic film as an intermediate process.
このようなりTB法を利用した平版印刷材料は、原稿像
が左右逆像とならないように、プリズムあるいは反射ミ
ラーなどの像反転機構を内蔵した専用の製版カメラで撮
影から製版処理まで自動的に行われている。Lithographic printing materials using the TB method use a special plate-making camera with a built-in image reversal mechanism such as a prism or reflective mirror to prevent the original image from being left-right reversed, from photographing to plate-making automatically. It is being said.
こめような製版カメラは、高価であるだけでなく、像反
転機構により像の解像性を低下させるという欠点がある
。Such a prepress camera is not only expensive, but also has the disadvantage that the image reversal mechanism reduces image resolution.
像反転機構を有しない製版カメラで正像の平版印刷版を
得るためには、特開昭48−89007に記載されてい
る様に、平版印刷材料の支持体を介して、即ち、支持体
製側から原稿の像様無光を行う方法が公知である。本明
細曹に於ては、この露光方法を裏焼きという。In order to obtain a lithographic printing plate with a normal image using a plate-making camera that does not have an image reversal mechanism, as described in Japanese Patent Laid-Open No. 48-89007, it is necessary to Methods are known for performing imagewise aphoticization of documents from the side. In this specification, this exposure method is referred to as back printing.
ニ方、DTR法を利用した平版印刷材料は機械的摩耗に
対する抵抗性が不十分でインキ像を担持する疎水性部域
が欠落したり、あるいは、徐々にそのインキ受容性を失
わせしめる為、耐刷力の低下を招く欠点を有する。親水
性部域に於ては、機械的摩耗に依り、徐々に疎水化し、
非画線地部域がインキで汚れる様になυ、疎水性像部域
に於ては、均一脂性インキ受理性に欠陥を生じ、これが
上記像部域にインキ受理性の変動を生せしめ、従って印
刷される部域が均一量のインキを受は入れられない様に
なる。その他の平版印刷版でもそうである様に、DTR
法を利用した平版印刷材料に於ても版材の構成、処理液
の構成あるいは印刷条件等により耐刷力を増強せしめる
事が要求され、各種改良がされてきた。特公昭48−3
0562に基本的に記述されている平版印刷材料につい
ても同様で特公昭51〜15765、同51〜1680
3、特開昭51〜111103、同52−150105
、同53−9603二同54−135002、同55−
7704、同55−100554、同56−27151
、同57−86835、同58−196548など印刷
性は著しく向上している。特に特開昭55−10055
4、同58−196548に教示されている下塗層への
2〜10μのマット剤の添加は版面の保水性の向上及び
著しい耐刷力の向上をもたらす。On the other hand, lithographic printing materials using the DTR method have insufficient resistance to mechanical abrasion, resulting in the loss of hydrophobic areas that carry ink images or gradual loss of ink receptivity. It has the disadvantage of reducing printing force. Hydrophilic areas gradually become hydrophobic due to mechanical abrasion,
As the non-image areas become smeared with ink, in the hydrophobic image areas there is a defect in uniform oily ink receptivity, which causes variations in ink receptivity in the image areas, Therefore, the area to be printed will not receive a uniform amount of ink. As with other lithographic printing plates, DTR
Even in lithographic printing materials using this method, there is a need to increase the printing durability by changing the composition of the plate material, the composition of the processing liquid, printing conditions, etc., and various improvements have been made. Special Public Service 1977-3
The same applies to the lithographic printing materials basically described in 0562.
3. Japanese Patent Publication No. 51-111103, 52-150105
, 53-9603 2 54-135002, 55-
7704, 55-100554, 56-27151
, 57-86835, and 58-196548, the printability has been significantly improved. Especially JP-A-55-10055
4, No. 58-196548, the addition of a matting agent of 2 to 10 .mu.m to the undercoat layer improves the water retention of the plate surface and significantly improves the printing durability.
しかし、この様なマット剤を含む下塗り層ヲ用い、うら
焼きでの高い細線の再現性及び耐刷力を得る為に、下塗
り層にハレーション防止剤を通常の濃度で適用した場合
、うら焼きでの写真特性の軟調化を引き起こした。DT
R法を利用した平版印刷材料に於て、写真特性の軟調化
は、細線の耐刷の低下を引き起こすものであり、本来の
目的と相反するものである。その為、高い細線の耐刷力
を持つ、うら焼き用のIJTR法を利用した平版印刷材
料が必要となっている。However, when using an undercoat layer containing such a matting agent and applying an antihalation agent at a normal concentration to the undercoat layer in order to obtain high reproducibility of fine lines and printing durability in glazing, This caused a softening of the photographic characteristics. DT
In planographic printing materials using the R method, softening of photographic characteristics causes a decrease in printing durability of fine lines, which is contrary to the original purpose. Therefore, there is a need for a lithographic printing material using the IJTR method for back printing that has high printing durability for fine lines.
(C) 発明の目的
本発明の目的は、細線再現性に優れ、写真特性が硬調で
高耐刷のうら焼き用のDTR法を利用した平版印刷材料
を提供することである。(C) Object of the Invention The object of the present invention is to provide a lithographic printing material using the DTR method for back printing, which has excellent fine line reproducibility, high contrast photographic characteristics, and high printing durability.
(Dl 発明の構成
本発明の目的は、支持体上に順に下塗層)・ロゲン化銀
乳剤層及び物理現像核層を少なくとも有するうら焼き可
能な平版印刷材料に於て、前記下塗層に0.1〜0.5
の透過濃度を与えるノーレージ履ン防止剤と平均粒径2
〜10μmのマット剤を含む事を特徴とするうら焼き用
平版印刷材料に依り達成された。(Dl Structure of the Invention The object of the present invention is to provide an undercoat layer on a support in order) - In a lithographic printing material that can be backprinted and has at least a silver halide emulsion layer and a physical development nucleus layer, the undercoat layer 0.1-0.5
A no-rage anti-wear agent and an average particle size of 2 to give a transmission density of
This was achieved using a lithographic printing material for overlaying, which is characterized by containing a matting agent of ~10 μm.
通常、表(乳剤層の側)から露光を行う場合の細線再現
性の低下の原因としては、支持体での光の反射に依るノ
・レーション乳剤層のノ・ロゲン化銀粒子での光散乱に
依るイラジェーションが知られている。Normally, when exposure is performed from the front (emulsion layer side), the causes of decreased fine line reproducibility include light reflection due to the support, light scattering by the silver halogenide grains in the emulsion layer, and It is known that irradiation is caused by
イラジェーション防止染料又は顔料全うら焼き用のDT
R法を利用した平版印刷材料に適用する事は、特開昭4
8−89007に示されているが、下塗9層に2〜10
μのマット剤を用いた高耐刷、高保水性のDTR法を利
用した平版印刷材料に於いては、良好な細線の耐刷は得
られない。DT for full irradiation of anti-irradiation dyes or pigments
The application of the R method to lithographic printing materials was disclosed in Japanese Unexamined Patent Publication No. 4
8-89007, but 2 to 10 layers are added to 9 layers of undercoat.
In a lithographic printing material using a DTR method with high printing durability and high water retention using a μ matting agent, good printing durability of fine lines cannot be obtained.
ハレーション防止剤は、下塗り層に加える方法とうら塗
り層へ加える方法が公知であるが、ここで述べる高耐刷
、高保水性のうら焼き用のDTR法を利用した平版印刷
材料に於ては、うら塗り層でのハレーシコン防止は効果
が小さく、下塗υ層でのハレーション防止のみが有効で
あった。There are known methods for adding antihalation agents to the undercoat layer and to the backcoat layer, but in the lithographic printing material using the DTR method for back printing with high printing durability and high water retention described here, The effect of preventing halation in the back coating layer was small, and only the prevention of halation in the undercoat υ layer was effective.
更に通常の表(乳剤層側)から露光を行う場合には、ハ
レーション防止層は、光学濃度を高くし、支持体からの
反射光の吸収を大きくする程、良好な細線再現性が得ら
れる。特開昭57−35854号には、表から露光を行
うDTR法を利用した平版印刷材料に於いて、耐刷力の
充分に強い細線のDT几面画像得るには、支持体(・・
レージ・ン防止層を含む)が0.6以上の光学濃度(好
ましくは、1.0以上の光学濃度)である事が必要であ
ると示されている。Furthermore, when exposure is performed from the normal front side (emulsion layer side), the higher the optical density of the antihalation layer and the greater the absorption of reflected light from the support, the better the fine line reproducibility will be obtained. JP-A No. 57-35854 discloses that in order to obtain a thin line DT surface image with sufficient printing durability in a lithographic printing material using the DTR method in which exposure is performed from the front side, a support (...
It is shown that it is necessary for the optical density (including the anti-resin layer) to be 0.6 or more (preferably 1.0 or more).
ところが、下塗シ層に2〜10μのマット剤を含む、高
耐刷、高保水性のうら焼き用のDTR法を利用した平版
印刷材料に於いて、この様な高濃度のハレーション防止
下塗り層を用いると、うら焼き時の写真感度を低下させ
るだけでなく、著しい写真特性の軟調化を示した。DT
R刷版での写真特性の軟調化は、細線、網点等の耐刷力
を低下させるとともに「貼込み原稿」を使用した場合、
「貼込み跡」を刷版上に記録するという重大な欠陥をも
たらすものである。However, in lithographic printing materials using the DTR method for overprinting with high printing durability and high water retention, in which the undercoat layer contains a matting agent of 2 to 10 μm, such a highly concentrated antihalation undercoat layer is used. This not only lowered the photographic sensitivity during back-printing, but also significantly softened the photographic characteristics. DT
The softening of the photographic characteristics of the R printing plate reduces the printing durability of fine lines, halftone dots, etc., and when using a "pasted original",
This results in a serious defect in that "pasting marks" are recorded on the printing plate.
又、下塗beへ2〜10μのマット剤を用いない場合は
前述の写真特性の軟調化は起こらなくなるが、この場合
、特開昭58−196548に示されている様に耐刷力
、保水性の平版印刷版としての基本的な性能が著しく低
下する。In addition, if a matting agent of 2 to 10 μm is not used in the undercoat be, the above-mentioned softening of the photographic properties will not occur, but in this case, the printing durability and water retention will be reduced as shown in JP-A-58-196548. The basic performance of the lithographic printing plate is significantly reduced.
従って、高耐刷、高保水性で写真特性が硬調で、且つ細
線再現性の優れた高品質のうら焼き用のDTR法を利用
した平版印刷材料を得る為には、下塗り層に2〜10μ
のマット剤を用い、より低い光学濃度のハレーション防
止下塗層を用いて、良好な細線再現性と細線の耐刷を得
る事が必要である。Therefore, in order to obtain a high-quality lithographic printing material using the DTR method for overlaying, which has high printing durability, high water retention, high contrast photographic properties, and excellent fine line reproducibility, it is necessary to add 2 to 10 μm in the undercoat layer.
It is necessary to use a matting agent and an antihalation undercoat layer with a lower optical density to obtain good fine line reproducibility and fine line printing durability.
ハレーション防止下塗層の光学′11k度は、0,1〜
0.5に設定される必要があり、0.1以下では充分な
細線再現性及び耐刷が得られず、0.5以上では写真特
性が軟調化し、種々の問題をひき起こす。The optical '11k degree of the antihalation undercoat layer is 0.1~
If it is less than 0.1, sufficient fine line reproducibility and printing durability cannot be obtained, and if it is more than 0.5, the photographic characteristics become soft, causing various problems.
光学濃度0.1〜0.5は表から露光されるべきDTR
法を利用した平版印刷材料のハレーション防止層の濃度
(1,0以上)に比べ著しく小さい値であるが、うら焼
きの場合、支持体は感光層より、製版カメラ上での光路
では前方(原稿側)に存在する為、比較的、支持体での
反射光の細線再現性への影響は小さいのであろう。Optical density 0.1-0.5 is DTR to be exposed from the front
This value is significantly smaller than the density of the antihalation layer (1.0 or more) in lithographic printing materials using the method, but in the case of back printing, the support is located in front of the photosensitive layer in the optical path on the platemaking camera (original). side), the effect of light reflected on the support on fine line reproducibility is probably relatively small.
ハレ−ション防止層としては、任意のハレーシラン防止
染料又は顔料を用いることが出来るが、カーボンブラッ
クを用いるのが最も好ましい。カーボンブラックはバイ
ンダー(ゼラチンが好ましい)に対して1〜5重量%の
範囲で用いるのが好ましい。Any antihalation dye or pigment can be used in the antihalation layer, but carbon black is most preferably used. Carbon black is preferably used in an amount of 1 to 5% by weight based on the binder (preferably gelatin).
本発明に於ける平均粒径2〜10μのマット4Jとして
は、シリカ、クレー、タルク、シークライトナトノ無機
マット剤及び米でんぷん、ポリメチルメタクリレート、
ポリスチレン、セルロースアセテートプロピオネートな
どの有機マット剤が挙げられるが特に好ましくは、平均
粒径4〜10μmのシリカ粒子である。これらのマット
剤の使用量は下塗層には親水性コロイドバインダーに対
して5〜40重量%程度である。ハロゲン化銀乳剤に含
む場合には親水性コロイドバインダーに対して1〜20
重量%程度であり、下塗層に用いたマット剤よりも少な
く用いる。一般的に、親水性コロイドバインダーに対す
る割合として、1/2〜1/10程度を目安にすること
が出来る。In the present invention, the matte 4J having an average particle size of 2 to 10 μm includes silica, clay, talc, Seecrite nano inorganic matting agent, rice starch, polymethyl methacrylate,
Examples include organic matting agents such as polystyrene and cellulose acetate propionate, but particularly preferred are silica particles with an average particle size of 4 to 10 μm. The amount of these matting agents used in the undercoat layer is about 5 to 40% by weight based on the hydrophilic colloid binder. 1 to 20 relative to the hydrophilic colloid binder when included in the silver halide emulsion.
It is about % by weight, and is used in a smaller amount than the matting agent used in the undercoat layer. Generally, the ratio to the hydrophilic colloid binder can be set at about 1/2 to 1/10.
本発明に於ける下塗層はセラチン単独又はゼラチンと特
開昭55−100554に記載の如き親水性コロイドや
アルギン酸ナトリウム、繊維素誘導体、ポリビニルアル
コール、ポリビニルピロリドンなど親水性コロイドとの
組合わせで用いることが出来る。セラチン層の硬化剤と
しては、ホルマリン、ムコクロル酸、ゲルタールアルデ
ヒド、シリカキサール、特開昭54−130936に記
載の如き初期縮合物、活性ハロゲン型、エチレンイキン
型、ビニルスルホン型、エポキシ型、あるいはクロム塩
の様な公知のものを使用できる。The undercoat layer in the present invention uses seratin alone or in combination with gelatin and hydrophilic colloids such as those described in JP-A-55-100554, sodium alginate, cellulose derivatives, polyvinyl alcohol, and polyvinylpyrrolidone. I can do it. As the curing agent for the ceratin layer, formalin, mucochloric acid, geltaraldehyde, silicaxal, an initial condensate as described in JP-A-54-130936, active halogen type, ethylene quine type, vinyl sulfone type, epoxy type, or chromium can be used. Known substances such as salt can be used.
本発明の平版印刷材料に用いられる支持体は、原稿から
の撮影光が支持体を介してハロゲン化銀乳剤層に到達す
る必要があるため、光透過性の支持体が用いられ、例え
ばフィルム(酢酸セルロースフィルム、ポリビニルアセ
タールフィルム、ポリスチレンフィルム、ポリプロピレ
ンフィルム、ポリエチレンテレフタレートフィルム)、
ポリエステル、ポリプロピレン又はポリスチレンフィル
ム等をポリエチレンフィルムで被覆した複合フィルム等
が挙けられる。淳みは任意であるが、50〜200j1
mの範囲が好ましい。The support used in the lithographic printing material of the present invention is a light-transmissive support, such as a film ( cellulose acetate film, polyvinyl acetal film, polystyrene film, polypropylene film, polyethylene terephthalate film),
Composite films such as polyester, polypropylene, or polystyrene films coated with polyethylene films may be mentioned. Atsushi is optional, but 50-200j1
A range of m is preferred.
感光性ハロゲン化銀乳剤層は当分針で公知のものが全て
用いることが出来るが、好ましくは特開昭49−554
02に記載のようなものである。As the photosensitive silver halide emulsion layer, all known ones can be used, but preferably those made in Japanese Patent Application Laid-open No. 49-554
This is as described in 02.
物理現像核層も特公昭48−30562、特開昭49−
55402、同53−21602等に記載されている全
てが用いられる。The physical development nucleus layer is also JP-B No. 48-30562, JP-A No. 49-Sho.
55402, 53-21602, etc. can be used.
硝酸銀として表わしたハロゲン化銀に対する親水性コロ
イドの重量比は、一般に3〜0.2、好ましくは1.5
〜0.3である。支持体上に存在させるハロゲン化銀の
量は約0.2〜約5g7m”、好ましくは0.5〜3g
/mlの硝酸銀に等しくなるように被覆する。The weight ratio of hydrophilic colloid to silver halide, expressed as silver nitrate, is generally between 3 and 0.2, preferably 1.5.
~0.3. The amount of silver halide present on the support is from about 0.2 to about 5 g7m'', preferably from 0.5 to 3 g.
/ml silver nitrate.
物理現像核としては、アンチモン、ビスマス、カドミウ
ム、コバルト、パラジウム、ニッケル、銀、鉛、亜鉛な
どの金属およびそれらの硫化物など公知のものが使用し
うる。物理現像核層には、親水性コロイドヲ含んでいな
くてもよく、ゼラチン、カルボキシメチルセルロース、
アラビアゴム、アルキン酸ナトリウム、ヒドロキシエチ
ル澱粉、デキストリン、ヒドロキシエチルセルロース、
ポリスチレンスルホン酸、ビニルイミタゾールとアクリ
ルアミドとの共重合体、ポリビニルアルコール等の親水
性ヲロイドを含むこともできる。As the physical development nucleus, known metals such as antimony, bismuth, cadmium, cobalt, palladium, nickel, silver, lead, zinc, and their sulfides can be used. The physical development nucleus layer does not need to contain hydrophilic colloids, and may include gelatin, carboxymethyl cellulose,
Gum arabic, sodium alkinate, hydroxyethyl starch, dextrin, hydroxyethyl cellulose,
Hydrophilic holoids such as polystyrene sulfonic acid, a copolymer of vinyl imitazole and acrylamide, and polyvinyl alcohol may also be included.
核層中には、吸湿性物質、例えばソルビトール、グリセ
ロールなどの湿潤剤全存在させてもよい。Hygroscopic substances, such as wetting agents such as sorbitol and glycerol, may be present entirely in the core layer.
さらに、核層中には、硫酸バリウム二酸化チタン、チャ
イナクレーおよび銀などのスカミング防止のための顔料
およびホルムアルデヒドの如き硬膜剤さらには錯化剤も
含有しうる。Furthermore, the core layer may also contain pigments for preventing scumming, such as barium titanium sulfate dioxide, china clay and silver, and hardeners, such as formaldehyde, as well as complexing agents.
本発明で使用するDTI’L処理溶液は、アルカリ性物
質、例えば水酸化ナトリウム、水酸化カリウム、第三燐
酸す) IJウム等、保恒剤としての亜硫酸t、111
m剤、例えば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、かぶり防止剤、例えば臭化カリウム
、1〜フェニル−5−メにカプトテトラゾール、錯化剤
、例えばチオ硫酸塩、チオシアンrR塩、環状イミド、
チオサリチル酸等現m 剤例えはハイドロキノン、1〜
フェニル−3−ピラゾリドン、p−メチルフェノール等
、現像変性剤、例えはポリオキシアルキレン化合物、オ
ニウム化合物等を含むことができる。The DTI'L treatment solution used in the present invention contains alkaline substances such as sodium hydroxide, potassium hydroxide, tertiary phosphate, etc., sulfite as a preservative, 111
m-agents such as hydroxyethyl cellulose, carboxymethyl cellulose, antifoggants such as potassium bromide, 1-phenyl-5-mer captotetrazole, complexing agents such as thiosulfates, thiocyan rR salts, cyclic imides,
Examples of agents such as thiosalicylic acid are hydroquinone, 1-
Phenyl-3-pyrazolidone, p-methylphenol, etc., development modifiers, such as polyoxyalkylene compounds, onium compounds, etc. can be included.
本発明の平版印刷版は、例えは特公昭48−29723
、米国特許第3,721.559号明細書に記載されて
いる如き化合物でインキ受理性に変換ないしは増強しう
る。印刷方法あるいは使用する不感脂化液、給湿液など
は普通によく知られた方法による事が出来る。The lithographic printing plate of the present invention is, for example,
, U.S. Pat. No. 3,721.559, can be used to convert or enhance ink receptivity. The printing method, the desensitizing liquid, the dampening liquid, etc. used can be generally well-known methods.
(匂 実施例
以下に本発明を実施例に依り説明するが、勿論これだけ
に限定されるものではない。(Smell) Examples The present invention will be explained below with reference to examples, but of course it is not limited to these examples.
175jmのポリエステルフィルムの両面に20μmの
ポリエチレンを?[1し、支持体裏面をコロナ数値処理
後、うら塗9層を設けた後、支持体表面をコロナ放11
L後、カーボンブラックの添加量を変えた(表1、ム〜
E)、平均粒径7μmのシリカ(0,68/m’)?含
む下塗りNI(セラチン3゜58/rIL″)と、七の
上に万ル鰺増感された高コントラスト塩化銀乳剤(セラ
テン1.08/m″)tl−硝酸銀としてL517m″
で窪布した。加温硬′#4後、特開昭57−8b835
の実施例1の試料Jと同じ核塗液を塗布して平版印柚j
材料とした。20μm polyethylene on both sides of 175jm polyester film? [1] After applying corona numerical treatment to the back side of the support and applying 9 layers of back coating, the surface of the support was subjected to corona radiation 11
After L, the amount of carbon black added was changed (Table 1,
E), silica with an average particle size of 7 μm (0,68/m')? An undercoat containing NI (Ceratin 3°58/m") and a high contrast sensitized silver chloride emulsion (Ceratin 1.08/m") on top of seven tl-silver nitrate L517m"
It was Kubobu. After heating and hardening #4, JP-A-57-8B835
The same core coating liquid as Sample J of Example 1 was applied to make a planographic impression.
It was used as a material.
像反転機構を有しない製版カメラの原稿架に濃度中1.
5のウェッジ画像と線幅の異なる細線及びアミ点画伽と
金含む版下原稿t−準備し、これらの試料の裏側から原
稿’!に3!Ik* L、これらの試料の裏側から原稿
を反射光にて撮影し、下記の転写現像液で30″Cl2
O秒間税像処理した。The density 1.
5 wedge images, fine lines with different line widths, tint dots, and gold. To 3! Ik*L, the originals were photographed from the back side of these samples using reflected light, and the following transfer developer was used at 30"Cl2.
The image was processed for 0 seconds.
現像処理後、核原版を2不の絞りローラー間を通し、余
分の現像液を除去し、直ちに下記組成を有する中和液で
25℃、20秒間処理し、絞りローラーで余分の液を除
去し、室温で乾燥した。After the development process, the nuclear master plate was passed between two squeezing rollers to remove excess developer, and immediately treated with a neutralizing solution having the following composition at 25°C for 20 seconds, and the excess liquid was removed using a squeezing roller. , dried at room temperature.
転写現f!に’a
中和液
以上の操作により作製した平版印刷版をオフセット印刷
機に装看し、下記不感脂化准を版面にく17にく与え、
下記給湿液を用いて卵桐を行なった。Transcription f! ni'a Neutralizing solution Load the lithographic printing plate prepared by the above operations into an offset printing machine, apply the following desensitization agent to the plate surface,
Egg paulownia was carried out using the following dampening solution.
不感脂化液 耐 湿 液 表2 g度はl 0jlXBスケールで示しである。Desensitizing liquid Moisture resistant liquid Table 2 Degrees of g are shown on the l0jlXB scale.
結果を表2に示す。The results are shown in Table 2.
試料Aを良好Oとした場合の相対評価で、Δはヤヤ劣る
、×μ者しく劣るを表わす。In the relative evaluation when sample A is considered to be good, Δ represents very poor, ×μ represents very poor.
CIlCl1t力〕 5Uaの細縁での評価を行なった。CIlCl1t force] Evaluation was performed using a narrow edge of 5 Ua.
1・・・・・・・・・ 5.000枚以下2・・・・・
・・・・ 5,000〜10.000枚3・・・・・・
・・・10.000枚以上(F′)発明の効果
本発明は、像反転機構を有しない製版カメラとDTR法
を用いて左右正像が得られる裏焼用平版印刷材料であり
、細線再現性にすぐれ、写真特性が硬調で高耐刷、高保
水性の平版印刷材料である。1... 5,000 sheets or less 2...
・・・・・・ 5,000-10,000 sheets 3・・・・・・
...10,000 sheets or more (F') Effects of the invention The present invention is a back printing lithographic printing material that can obtain left and right images using a plate making camera without an image reversal mechanism and the DTR method, and is capable of fine line reproduction. It is a lithographic printing material with excellent properties, high contrast, high printing durability, and high water retention.
Claims (1)
像核層を少なくとも有する裏焼き可能な平版印刷版に於
て、前記下塗層に0.1〜0.5の透過濃度を与えるハ
レーション防止剤と、平均粒径2〜10μmのマット剤
を含む事を特徴とする裏焼き用平版印刷材料。In a back-baking lithographic printing plate having at least an undercoat layer, a silver halide emulsion layer and a physical development nucleus layer in this order on a support, the undercoat layer is given a transmission density of 0.1 to 0.5. A lithographic printing material for back printing, characterized in that it contains an antihalation agent and a matting agent with an average particle size of 2 to 10 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6148087A JPS63226658A (en) | 1987-03-16 | 1987-03-16 | Planographic printing material for back exposure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6148087A JPS63226658A (en) | 1987-03-16 | 1987-03-16 | Planographic printing material for back exposure |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63226658A true JPS63226658A (en) | 1988-09-21 |
JPH0447300B2 JPH0447300B2 (en) | 1992-08-03 |
Family
ID=13172281
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6148087A Granted JPS63226658A (en) | 1987-03-16 | 1987-03-16 | Planographic printing material for back exposure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63226658A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0566564A (en) * | 1991-09-10 | 1993-03-19 | Mitsubishi Paper Mills Ltd | Planographic printing plate |
JPH0580519A (en) * | 1991-09-19 | 1993-04-02 | Mitsubishi Paper Mills Ltd | Planographic printing plate |
JPH0580517A (en) * | 1991-09-19 | 1993-04-02 | Mitsubishi Paper Mills Ltd | Planographic printing plate for back exposure |
JPH05100430A (en) * | 1991-10-04 | 1993-04-23 | Mitsubishi Paper Mills Ltd | Planographic printing plate |
JPH05107765A (en) * | 1991-10-14 | 1993-04-30 | Mitsubishi Paper Mills Ltd | Planographic printing plate |
CN102411262A (en) * | 2010-09-26 | 2012-04-11 | 比亚迪股份有限公司 | Film, its preparation method and using method |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58196548A (en) * | 1982-05-13 | 1983-11-16 | Mitsubishi Paper Mills Ltd | Lithographic printing plate |
JPS6025777A (en) * | 1983-07-22 | 1985-02-08 | Janome Sewing Mach Co Ltd | Nylon sintered body for ink impregnated platen of ink platen type printer |
-
1987
- 1987-03-16 JP JP6148087A patent/JPS63226658A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58196548A (en) * | 1982-05-13 | 1983-11-16 | Mitsubishi Paper Mills Ltd | Lithographic printing plate |
JPS6025777A (en) * | 1983-07-22 | 1985-02-08 | Janome Sewing Mach Co Ltd | Nylon sintered body for ink impregnated platen of ink platen type printer |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0566564A (en) * | 1991-09-10 | 1993-03-19 | Mitsubishi Paper Mills Ltd | Planographic printing plate |
JPH0580519A (en) * | 1991-09-19 | 1993-04-02 | Mitsubishi Paper Mills Ltd | Planographic printing plate |
JPH0580517A (en) * | 1991-09-19 | 1993-04-02 | Mitsubishi Paper Mills Ltd | Planographic printing plate for back exposure |
JPH05100430A (en) * | 1991-10-04 | 1993-04-23 | Mitsubishi Paper Mills Ltd | Planographic printing plate |
JPH05107765A (en) * | 1991-10-14 | 1993-04-30 | Mitsubishi Paper Mills Ltd | Planographic printing plate |
CN102411262A (en) * | 2010-09-26 | 2012-04-11 | 比亚迪股份有限公司 | Film, its preparation method and using method |
Also Published As
Publication number | Publication date |
---|---|
JPH0447300B2 (en) | 1992-08-03 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |