EP1486348B1 - Method of producing a planographic printing plate - Google Patents
Method of producing a planographic printing plate Download PDFInfo
- Publication number
- EP1486348B1 EP1486348B1 EP04076742A EP04076742A EP1486348B1 EP 1486348 B1 EP1486348 B1 EP 1486348B1 EP 04076742 A EP04076742 A EP 04076742A EP 04076742 A EP04076742 A EP 04076742A EP 1486348 B1 EP1486348 B1 EP 1486348B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- aluminium
- support
- weight
- plate
- etching
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 60
- 239000004411 aluminium Substances 0.000 claims description 71
- 229910052782 aluminium Inorganic materials 0.000 claims description 71
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 71
- 238000005266 casting Methods 0.000 claims description 27
- 238000005530 etching Methods 0.000 claims description 26
- 229910000838 Al alloy Inorganic materials 0.000 claims description 18
- 238000009749 continuous casting Methods 0.000 claims description 18
- 238000010438 heat treatment Methods 0.000 claims description 11
- 238000005097 cold rolling Methods 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- 239000012670 alkaline solution Substances 0.000 claims description 6
- 238000007788 roughening Methods 0.000 claims description 6
- 238000007743 anodising Methods 0.000 claims description 4
- 238000004381 surface treatment Methods 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 29
- 239000000243 solution Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 239000003513 alkali Substances 0.000 description 10
- 239000001117 sulphuric acid Substances 0.000 description 10
- 235000011149 sulphuric acid Nutrition 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 229910045601 alloy Inorganic materials 0.000 description 9
- 239000000956 alloy Substances 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000010410 layer Substances 0.000 description 9
- 235000011121 sodium hydroxide Nutrition 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 238000011161 development Methods 0.000 description 7
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000000866 electrolytic etching Methods 0.000 description 6
- 238000005096 rolling process Methods 0.000 description 6
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 5
- 238000000137 annealing Methods 0.000 description 5
- 238000007598 dipping method Methods 0.000 description 5
- 238000005098 hot rolling Methods 0.000 description 5
- 229910017604 nitric acid Inorganic materials 0.000 description 5
- 238000002203 pretreatment Methods 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000012937 correction Methods 0.000 description 4
- 230000005611 electricity Effects 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004115 Sodium Silicate Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 229910052911 sodium silicate Inorganic materials 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 229920000084 Gum arabic Polymers 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 241000978776 Senegalia senegal Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000205 acacia gum Substances 0.000 description 2
- 235000010489 acacia gum Nutrition 0.000 description 2
- 238000003486 chemical etching Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- JVICFMRAVNKDOE-UHFFFAOYSA-M ethyl violet Chemical compound [Cl-].C1=CC(N(CC)CC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 JVICFMRAVNKDOE-UHFFFAOYSA-M 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- 235000011118 potassium hydroxide Nutrition 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 235000019795 sodium metasilicate Nutrition 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 description 1
- AEQDJSLRWYMAQI-UHFFFAOYSA-N 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline Chemical compound C1CN2CC(C(=C(OC)C=C3)OC)=C3CC2C2=C1C=C(OC)C(OC)=C2 AEQDJSLRWYMAQI-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical class CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- LBBOQIHGWMYDPM-UHFFFAOYSA-N 2-tert-butylphenol;formaldehyde Chemical compound O=C.CC(C)(C)C1=CC=CC=C1O LBBOQIHGWMYDPM-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- -1 Ester compound Chemical class 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 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
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- HRBFQSUTUDRTSV-UHFFFAOYSA-N benzene-1,2,3-triol;propan-2-one Chemical compound CC(C)=O.OC1=CC=CC(O)=C1O HRBFQSUTUDRTSV-UHFFFAOYSA-N 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- VOOLKNUJNPZAHE-UHFFFAOYSA-N formaldehyde;2-methylphenol Chemical compound O=C.CC1=CC=CC=C1O VOOLKNUJNPZAHE-UHFFFAOYSA-N 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 239000000176 sodium gluconate Substances 0.000 description 1
- 235000012207 sodium gluconate Nutrition 0.000 description 1
- 229940005574 sodium gluconate Drugs 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- FGDMJJQHQDFUCP-UHFFFAOYSA-M sodium;2-propan-2-ylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(C(C)C)=CC=C21 FGDMJJQHQDFUCP-UHFFFAOYSA-M 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- ROVRRJSRRSGUOL-UHFFFAOYSA-N victoria blue bo Chemical compound [Cl-].C12=CC=CC=C2C(NCC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 ROVRRJSRRSGUOL-UHFFFAOYSA-N 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N1/00—Printing plates or foils; Materials therefor
- B41N1/04—Printing plates or foils; Materials therefor metallic
- B41N1/08—Printing plates or foils; Materials therefor metallic for lithographic printing
- B41N1/083—Printing plates or foils; Materials therefor metallic for lithographic printing made of aluminium or aluminium alloys or having such surface layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D11/00—Continuous casting of metals, i.e. casting in indefinite lengths
- B22D11/001—Continuous casting of metals, i.e. casting in indefinite lengths of specific alloys
- B22D11/003—Aluminium alloys
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N3/00—Preparing for use and conserving printing surfaces
- B41N3/03—Chemical or electrical pretreatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N3/00—Preparing for use and conserving printing surfaces
- B41N3/03—Chemical or electrical pretreatment
- B41N3/034—Chemical or electrical pretreatment characterised by the electrochemical treatment of the aluminum support, e.g. anodisation, electro-graining; Sealing of the anodised layer; Treatment of the anodic layer with inorganic compounds; Colouring of the anodic layer
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F1/00—Etching metallic material by chemical means
- C23F1/10—Etching compositions
- C23F1/14—Aqueous compositions
- C23F1/32—Alkaline compositions
- C23F1/36—Alkaline compositions for etching aluminium or alloys thereof
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F1/00—Electrolytic cleaning, degreasing, pickling or descaling
- C25F1/02—Pickling; Descaling
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F3/00—Electrolytic etching or polishing
- C25F3/02—Etching
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F3/00—Electrolytic etching or polishing
- C25F3/02—Etching
- C25F3/04—Etching of light metals
Definitions
- the present invention relates to a method of producing a planographic printing plate and more particularly a method in which the support is made using continuous casting.
- Conventional aluminium alloy substrates for a support for a lithographic printing plate are generally provided in the form of a 0.1 to 0.5 mm thick cold-rolled sheet made of an aluminium alloy such as JIS A1050, A1100, A3003, or the like.
- Such aluminium alloy cold-rolled sheets are generally produced by machining the surface of a semi continuous-cast (DC) slab or billet, homogenization heat-treating the billet when necessary, heating the billet to a selected temperature, hot-rolling the heated billet to a hot-rolled strip, cold-rolling the hot-rolled strip with an intermediate annealing between the cold rolling passes when necessary, and final cold rolling the strip to a cold-rolled sheet.
- the aforementioned conventional process using a DC slab or billet has drawbacks in that the process steps are complicated and take much time, the production cost is high, the casting speed is slow, the rolling and heat treatment conditions are strict, and heat treatments must be carried out many times, and the process cannot provide an aluminium alloy support with stable properties.
- Japanese Unexamined Patent Publication (Kokai) Nos. 3-79798 and 5-156414 disclosed a process of producing an aluminium alloy support for a lithographic printing plate, in which an aluminium alloy melt is continuously cast and rolled to form a strip, which is subjected to cold rolling, heat treatment, and straightening.
- EP-A-0 603 476 , US-A-6 156 135 and EP-A-0 640 694 describe further methods for producing printing plates. These known methods have the same disadvantages discussed above.
- the invention furthermore relates to a method for producing a planographic printing plate by casting molten aluminium directly and continuously into a thin aluminium plate, wherein the side that is the top side during the casting process is used for the manufacturing of the printing plate.
- directly and continuously casting has to be understood as at least encompassing various methods in which aluminium or aluminium alloy or similar suitable material is molten and then transferred to suitable equipment for forming thin sheet-like material in a continuous process.
- aluminium has to be understood as including aluminium alloys.
- the invention relates to a method for producing said printing plates.
- Heat/photo sensitive printing plate an aluminium plate provided with a heat and/or a photo-sensitive layer.
- Planographic printing plate an exposed(heat/photo) printing plate ready for usage in a printing process.
- a method for continuously cast rolling a tabular plate directly from molten aluminium alloy there can be used a method employing a cooling belt such as Hazelett method or a method employing a cooling roller such as Hunter method and 3C method. Since the Hazelett method continuously casts a thick plate, a hot rolling is subsequently conducted to make the thickness reelable. On the other hand, since the Hunter method or the 3C method makes it possible to directly cast a plate having the thickness of 10 mm or lower, a hot rolling machine is not necessary.
- JP-A-60-238001 , JP-A-60-240360 , etc. disclose a method for preparing a coil of thin sheet. Among those a twin roller continuous casting method such as the Hunter method is preferable. Preferably a substantially horizontal casting method is used.
- the molten aluminium alloy is rapidly cooled by the continuous casting.
- the reference number 1 is a melt holding furnace in which an aluminium ingot is melted and retained.
- the molten aluminium is then fed to a twin-roller continuous casting machine 2, then wound on coiler 3.
- a continuous casting method using a cooling belt and a hot rolling may be applied as shown in Fig. 1(B) .
- the coil wound on coiler 3 is cold rolled to a thin plate of 0.3 to 3.0 mm using cold rolling machine 4.
- an intermediate annealing may be conducted using heating machine 5 when necessary.
- heating (annealing) machine 5 there are various types such as a batch type, a continuous annealing type, an induced heating type.
- the temperature is elevated at a rate of 0.5 °C/sec or more and the preferred temperature is 300 °C or more. More preferably annealing can be applied at 480°C or more.
- the resulting thin plate is rolled again to a thickness of 0.1 to 0.5 mm using a cold rolling machine.
- correction is conducted using correcting machine 6. The correction may be conducted together with a finishing rolling.
- the aluminium support thus obtained is subjected to a graining treatment.
- an aluminium alloy support for a printing plate is electrolytically grained, it is a common practice to carry out as a pre-treatment chemical etching with an acid or alkali for degreasing or removal of oxide films from the surface of the substrate.
- the electrolytic graining process is an electrolytic etching process wherein an alternating current is applied where as a counter electrode graphite or the like is used to cause electrolytic etching, thereby forming pits on the surface of the substrate to provide a grained surface.
- the above graining enhances the adhesion of a photosensitive film and improves the water retention, beneficial to printing performance, to the printing plate. Since adhesion and water retention should be provided uniformly over the whole surface of the printing plate, pits should be formed uniformly over the whole printing plate. For a printing plate provided with a photosensitive film, the grained surface should have a uniform appearance when viewed with the naked eye because the results of development after the exposure and development are evaluated by visual inspection.
- Nonuniform appearance of the grained surface means nonuniform color tone such as observation of streaks (a streak pattern) along the rolling direction or partial loss of gloss to give a cloudy appearance. This is caused by nonuniform chemical etching as a pre-treatment, leaving at least one region unetched or excessive etching, and electrolytic etching as an electrolytic graining treatment and a nonuniform metallic structure.
- nonuniform metallic structure is attributable to nonuniform aluminium crystals orientation and aluminium crystal size, coarsening and nonuniform dispersion of an intermetallic compound, and the like. Even when the nonuniformity of the metallic structure is of an extent that is not detrimental to the uniformity of electrolytic graining (including pre-treatment) necessary for printing, it often makes the appearance of the grained surface remarkably nonuniform.
- a nonuniform appearance, i.e., the presence of cloudy color shading, in the grained surface is very inconvenient to inspection of image areas after development.
- the cloudy portions are present as they are in nonimage portions after development, and since they have a color tone similar to the image areas, it becomes difficult to visually judge whether or not the image areas can be satisfactorily developed.
- ripple mark defect a wave like pattern.
- the ripple marks become visible after a sequence of surface treatments and can only clearly be observed when the final product is almost completed.
- Etching operation can be done by simply dipping a sample in an alkali bath. Temperature is between 15 to 35 °C, dipping time is between 1 to 10 minutes, depending on alloy, thickness, casting conditions, etc..
- alkali etching method the more suitable surface for planographic printing plate can be determined. This method is in principle independent from the continuous cast method used. It can be applied to the supports obtained via any of the above mentioned continuous cast methods and even for such methods as described in for example US4523627 or WO9832559 .
- the side to be used for graining, hydrophilizing, coating, matting, etc. in order to form a good quality lithographic printing plate for supports manufactured via basically horizontal continuous casting methods was found to be the side that is the top side during the casting process.
- the present inventors discovered that usage of the side that was the bottom side during the casting as surface for subsequent graining, hydrophilizing, coating, matting, etc. runs a risk of providing a non-uniform surface, in the form of ripple marks.
- the top side during casting is much less prone to ripple mark formation, whereas the bottom side during casting quite often shows ripple marks.
- Usage of the top side drastically improves lot to lot fluctuation of casting in terms of ripple mark formation.
- the temperature in melt holding furnace 1 needs to be kept at not lower than the melting point of aluminium.
- the temperature in the melt holding furnace varies depending on the components of aluminium alloy. In general, it is not lower than 800 °C.
- the molten aluminium alloy is subjected to a proper treatment such as inert gas purge and fluxing.
- a preferable constitutional range of an alloy component is as follows.
- the preferable Fe content in the alloy is between 0.15 and 0.50 weight %, more preferably between 0.20 and 0.35 weight %.
- the preferable Si content is between 0.05 and 0.20 weight %, more preferably between 0.10 and 0.15 weight %.
- Si content is less than 0.05 weight %, response to electrical graining becomes weak.
- Si content is more than 0.20 weight %, toning characteristic of the printing plate becomes worse.
- the preferable Cu content is between 0.005 and 0.040 weight %, more preferably between 0.008 and 0.025 weight %.
- Cu content is less than 0.005 weight %, response to electrical graining becomes weak.
- Cu content is more than 0.040 weight %, resulting electrical graining structure becomes too coarse leading the printing plate having worse toning characteristic.
- the method for graining the support for planographic printing plate according to the present invention there is used mechanical graining, chemical graining, electrochemical graining or combination thereof.
- Examples of mechanical graining methods include ball graining, wire graining, brush graining, and liquid honing.
- electrochemical graining method there is normally used AC electrolytic etching method.
- electric current there is used a normal alternating current such as sine waveform or a special alternating current such as square waveform, and the like.
- etching may be conducted with caustic soda.
- electrochemical graining it is preferably conducted with an alternating current in an aqueous solution mainly composed of hydrochloric acid or nitric acid.
- aqueous solution mainly composed of hydrochloric acid or nitric acid.
- the aluminium support is etched with alkali.
- alkaline agents include caustic soda, caustic potash, sodium metasilicate, sodium carbonate, sodium aluminate, sodium gluconate, etc.
- concentration of the alkaline agent, the temperature of the alkaline agent and the etching time are preferably selected from 0.01 to 25%, 20 to 90 °C and 5 sec. to 5 min., respectively.
- the preferred etching rate is in the range of 0.1 to 15 g/m 2 .
- the etching rate is preferably in the range of 0.01 to 1 g/m 2 ( JP-A-1-237197 ). Since alkaline-insoluble substances (smut) are left on the surface of the aluminium plate thus alkali-etched, the aluminium plate may be subsequently desmutted as necessary.
- the aluminium plate is subsequently subjected to AC electrolytic etching in an electrolyte mainly composed of hydrochloric acid or nitric acid.
- the frequency of the AC electrolytic current is in the range of 0.1 to 100 Hz, preferably 0.1 to 1.0 Hz or 10 to 60 Hz.
- the concentration of the etching solution is in the range of 3 to 150 g/l, preferably 5 to 50 g/l.
- the Content of aluminium in the etching bath is preferably in the range of not more than 50 g/l, more preferably 2 to 20 g/l.
- the etching bath may contain additives as necessary. However, in mass production, it is difficult to control the concentration of such an etching bath.
- the electric current density in the etching bath is preferably in the range of 5 to 100 A/dm 2 , more preferably 10 to 80 A/dm 2 .
- the waveform of electric current can be properly selected depending on the required quality and components of aluminium support used but may be preferably the special alternating waveform described in U.S. Patent No. 4,087,341 (corresponding to JP-B-56-19280 ) and JP-B-55-19191 . (The term "JP-B" as used herein means an "examined Japanese patent publication").
- the waveform of electric current and the liquid conditions are properly selected depending on required electricity as well as required quality and components of aluminium support used.
- the aluminium plate which has been subjected to electrolytic graining is then subjected to dipping in an alkaline solution as a part of desmutting treatment to dissolve smutts away.
- an alkaline agent there may be used caustic soda or the like.
- the desmutting treatment is preferably effected at a pH value of not lower than 10 and a temperature of 25 to 60°C for a dipping time as extremely short as 1 to 10 seconds.
- the aluminium plate thus etched is then dipped in a solution mainly composed of sulphuric acid.
- the sulphuric acid solution is in the concentration range of 50 to 400 g/l, and the temperature range of 20 to 70 °C. If the concentration of sulphuric acid is more than 400 g/l or the temperature of sulphuric acid is more than 70 °C, the processing bath is more liable to corrosion. Further, if the aluminium plate is etched by more than 0.4 g/m 2 , the printing durability may be reduced. Thus, the etching rate is preferably controlled to not more than 0.4 g/m 2 , more preferably not more than 0.2 g/m 2 .
- an anodized film is formed in an amount of 0.1 to 10 g/m2, more preferably 0.3 to 5 g/m 2 .
- the anodizing conditions vary with the electrolyte used and thus are not specifically determined. In general, it is appropriate that the electrolyte concentration is in the range of 1 to 80% by weight, the electrolyte temperature is in the range of 5 to 70 °C, the electric current density is in the range of 0.5 to 60 A/dm 2 , the voltage is in the range of 1 to 100 V, and the electrolysis time is in the range of 1 second to 5 minutes.
- the grained aluminium plate having an anodized film thus obtained is stable and excellent in hydrophilicity itself and thus can directly form a heat- or photosensitive coat thereon. If necessary, the aluminium plate may be further subjected to a surface treatment.
- a silicate layer formed by the foregoing metasilicate of alkaline metal or an undercoating layer formed by a hydrophilic polymeric compound may be formed on the aluminium plate.
- an undercoating layer Before applying the main coating layer, an undercoating layer may be applied.
- the coating amount of the undercoating layer is preferably in the range of 5 to 150 mg/m 2 .
- a heat- and/or photosensitive coating is then formed on the aluminium plate thus treated, imagewise exposed to light, and then developed, to make a printing plate, which is then mounted in a printing machine for printing.
- an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled.
- the strip was cold rolled to a thickness of 2.2 mm, then annealed at 520°C for 8 hours, and further cold rolled to form an aluminium support of a thickness of 0.278 mm.
- the aluminium support was subjected to alkali etching.
- the material was dipped in an aqueous solution of 25 weight % sodium hydroxide at 21°C for 7 minutes, rinsed by running water, and dried.
- the top surface at the casting did not reveal any ripple formation.
- the top surface at the casting of the aluminium support was brush grained, etched with a 25% aqueous solution of sodium hydroxide at 50°C such that etched amount was 5 g/m2, after washing the etched plate with water, the plate was immersed in an aqueous sulphuric acid of 180 g/l at 50°C for 20 seconds to desmut the plate, and the plate was washed with water.
- the support was electrochemically grained in 9 g/l of an aqueous nitric acid solution using the alternating (wave form ) electric current described in Japanese Patent No. JP-B-55-19191 ).
- An anode surface oxide coating of 2.5 g/m2 was formed on the support in a 20% sulphuric acid, and then dried. Furthermore a silicate layer was formed on the surface by dipping in an 2.5 wt% aqueous sodium metasilicate solution at 25°C.
- the thus obtained aluminium plate was examined for non-uniform parts: the plate appeared uniform in graining quality and appearance. No non-uniformity was observed.
- the photosensitive planographic printing plate thus-prepared was subjected to exposure for 50 seconds with a metal halide lamp of 3 kW from a distance of 1 m. through a transparent negative film, and then it was subjected to development with a developing solution of the following composition, followed by gumming in gum arabic, whereby the planographic printing plates were prepared.
- Developing solution Chemical g/l Sodium sulphite 5.0 Benzyl alcohol 30 Sodium carbonate 5.0 Sodium isopropylnaphthalenesulfonate 12.0 Purified water to make 1 lt
- a printing test was carried out in a usual procedure using the planographic printing plate thus-prepared: 200.000 copies could be printed with a good quality.
- an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled.
- the strip was cold rolled to a thickness of 2.2 mm, then annealed at 520°C for 8 hours, and further cold rolled to form an aluminium support with a thickness of 0.278 mm.
- the aluminium support as such was subjected to alkali etching.
- the support was dipped in an aqueous solution of 25 weight % sodium hydroxide at 21°C for 7 minutes, rinsed by running water, and dried.
- the bottom surface at the casting revealed severe ripple formation.
- Example 2 the side that was the bottom side during the casting process was submitted to the same steps as in Example 1. Upon examination, the plate shows an severe wave-like pattern, which renders the substrate unsuitable for further usage as a substrate for a lithographic printing plate.
- an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled.
- the strip was cold rolled to a thickness of 2.2 mm, then annealed at 380°C for 4 hours, and further cold rolled to form an aluminium support with a thickness of 0.278 mm.
- a similar test was repeated 10 times.
- the top surface at the casting of the test material was brush grained, etched with a 25% aqueous solution of sodium hydroxide at 50°C such that etched amount was 5 g/m2, after washing the etched plate with water, the plate was immersed in an aqueous sulphuric acid of 180 g/l at 50°C for 20 seconds to desmut the plate, and the plate was washed with water.
- the support was electrochemically grained in 9 g/l of an aqueous nitric acid solution using the alternating ( wave form ) electric current in the manner as described in example 1.
- the quantity of electricity in the anode time became 180 coulomb/dm2.
- An anode surface oxide coating of 3.5 g/m2 was formed on the support in a 20% sulphuric acid, and then dried.
- Photosensitive solution Chemical g/m2 Ester compound of naphtoquinone-1,2-diazido-5-sulfonyl chloride and pyrogallol-acetone resin(*) 0.45 Cresol formaldehyde resin 1.10 t-Butyl phenol formaldehyde resin 0.05 Tetrahydrophtalic acid anhydride 0.09 Naphtoquinone-1,2-diazido-4-sulfonyl chloride 0.03 Ethyl violet 0.05 Megafac F-176 (fluorine containing surfactant, available from Dainippon Ink and Chemicals, Inc) 0.01 Methyl Ethyl ketone 6.0 1-Methoxy-2-propanol 4.0 (*) as disclosed in U.S. patent no. 3,635,709 (example 1)
- the photosensitive planographic printing plate thus-prepared was subjected to exposure for 50 seconds with a metal halide lamp of 3 kW from a distance of 1m through a transparent positive film, and then it was subjected to development with a developing solution consisting of a 2 wt% aqueous solution of sodium silicate having a SiO 2 /Na 2 O ratio of about 1.1 and furthermore containing sodium ethylenediaminetetraacetate (0.01 g/l).
- the development process is followed by water rinsing and subsequent gumming in gum arabic, whereby the planographic printing plates were prepared.
- a printing test was carried out in a usual procedure using the planographic printing plate thus-prepared. 200.000 copies with high quality were obtained from all 10 trials.
- an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled.
- the strip was cold rolled to a thickness of 2.2 mm, then annealed at 380°C for 4 hours, and further cold rolled to form an aluminium support with a thickness of 0.278 mm.
- a similar test was repeated 10 times.
- Each aluminium support formed as such was subjected to alkali etching as described in the Example 1.
- Five out of the ten bottom surfaces at the casting revealed strong ripple formation, and 5 revealed slight ripple formation.
- an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled.
- the strip was cold rolled to a thickness of 2.2 mm, then annealed at 520°C for 8 hours, and further cold rolled to form an aluminium support with a thickness of 0.278 mm.
- the aluminium support formed as such was subjected to alkali etching.
- the material was dipped in an aqueous solution of 25 weight % sodium hydroxide at 21°C for 7 minute, rinsed by running water, and dried.
- the top surface at the casting did not reveal any ripple formation.
- the bottom side during casting showed a clear, wave-like pattern know as ripple mark.
- the upper surface at the casting of the support was etched with a 25% aqueous solution of sodium hydroxide at 50°C such that etched amount was 5 g/m2, after washing the etched plate with water, the plate was immersed in an aqueous sulphuric acid of 180 g/l at 50°C for 20 seconds to desmut the plate, and the plate was washed with water.
- the support was electrochemically grained in 10 g/l of an aqueous nitric acid solution using the alternating (wave form ) electric current in the manner as described in example 1.
- the quantity of electricity in the anode time became 280 coulomb/dm2.
- An anode surface oxide coating of 3.5 g/m2 was formed on the support in a 20% sulphuric acid, and then dried.
- composition was coated on the aluminium plate thus-prepared in a dry coated weight of 1.0 g/m2 to provide a heat-sensitive layer.
- Cyanine dye A (having the structure shown below) 0.025 g Megafac F177 manufactured by DAINIPPON INK & CHEMICALS, INC. 0.01 g Ethyl violet Methyl ethyl ketone 0.05 1-Methoxy-2-propanol 20.1 g 2.7 g
- the thus obtained heat sensitive plate was imaged in a Creo Trendsetter model 3244, and developed in the developer described in Example 2. Printing plates of excellent quality with good uniform appearance were obtained.
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Description
- The present invention relates to a method of producing a planographic printing plate and more particularly a method in which the support is made using continuous casting.
- Conventional aluminium alloy substrates for a support for a lithographic printing plate are generally provided in the form of a 0.1 to 0.5 mm thick cold-rolled sheet made of an aluminium alloy such as JIS A1050, A1100, A3003, or the like. Such aluminium alloy cold-rolled sheets are generally produced by machining the surface of a semi continuous-cast (DC) slab or billet, homogenization heat-treating the billet when necessary, heating the billet to a selected temperature, hot-rolling the heated billet to a hot-rolled strip, cold-rolling the hot-rolled strip with an intermediate annealing between the cold rolling passes when necessary, and final cold rolling the strip to a cold-rolled sheet.
- The aforementioned conventional process using a DC slab or billet has drawbacks in that the process steps are complicated and take much time, the production cost is high, the casting speed is slow, the rolling and heat treatment conditions are strict, and heat treatments must be carried out many times, and the process cannot provide an aluminium alloy support with stable properties.
- Japanese Unexamined Patent Publication (Kokai) Nos.
3-79798 5-156414 - The process disclosed in Japanese Unexamined Patent Publication (Kokai) Nos.
3-79798 5-156414 - The process described in
EP-A-0 640 694 , in which an aluminium alloy printing plate support is manufactured with the continuous casting method which obtains improved electrolytic graining quality by tight specifications of alloying elements as Cu, Si and Fe is improving the situation, although it still does not provide a sufficiently uniform surface. More specifically a significant amount of surface defects are visible after the printing plate manufacturing which are named ripple marks. These ripple marks can only be noticed after the process of manufacturing the presensitised printing plate is completed. This can give a lot of waste and a very cost inefficient process. -
EP-A-0 603 476 ,US-A-6 156 135 andEP-A-0 640 694 describe further methods for producing printing plates. These known methods have the same disadvantages discussed above. - It is an object of the present invention to provide a printing plate comprising at least a roughened and anodized aluminium plate provided with a heat or photosensitive material, wherein the roughened and anodized aluminium plate is formed from a thin aluminium support, which is made by casting molten aluminium directly and continuously, having a first suface and an opposite second surface where of the first and second surface the surface of the support which shows the least ripple marks upon etching with an alkaline solution has been used for roughening, anodizing and applying the heat or photo sensitive material.
- The invention furthermore relates to a method for producing a planographic printing plate by casting molten aluminium directly and continuously into a thin aluminium plate, wherein the side that is the top side during the casting process is used for the manufacturing of the printing plate.
- In this respect directly and continuously casting has to be understood as at least encompassing various methods in which aluminium or aluminium alloy or similar suitable material is molten and then transferred to suitable equipment for forming thin sheet-like material in a continuous process. In this application aluminium has to be understood as including aluminium alloys.
- The invention relates to a method for producing said printing plates.
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Fig. 1(A) illustrates the concept of an embodiment of the continuous casting process of the present invention, in which 1 indicates a melt holding furnace, 2 indicates a twin-roller continuous casting machine, and 3 indicates a coiler; -
Fig. 1(B) illustrates the concept of another embodiment of the continuous cast rolling process of the present invention, in which 1 indicates a melt holding furnace, 4 indicates a cold rolling machine, 7 indicates a twin-belt continuous casting machine, and 8 indicates a hot rolling machine; -
Fig. 1(C) illustrates the concept of an embodiment of the cold rolling process of the present invention, in which 4 indicates a cold rolling machine; -
Fig. 1(D) illustrates the concept of an embodiment of the heating process of the present invention, in which 5 indicates a heating machine; and -
Fig. 1(E) illustrates the concept of an embodiment of the correction process of the present invention, in which 6 indicates a correction machine. - It is an object of the present invention to provide a printing plate comprising at least a roughened and anodized aluminium plate provided with a heat or photosensitive material, wherein the roughened and anodized aluminium plate is formed from a thin aluminium support, which is made by casting molten aluminium directly and continuously, having a first suface and an opposite second surface where of the first and second surface the surface of the support which shows the least ripple marks upon etching with an alkaline solution has been used for roughening, anodizing and applying the heat or photo sensitive material.
- In this description the following definitions are used:
- (aluminium) Support or (aluminium) strips: the product of a continuous casting process.
- (aluminium) Plate: the support roughened by surface treatment.
- Heat/photo sensitive printing plate: an aluminium plate provided with a heat and/or a photo-sensitive layer.
- Planographic printing plate: an exposed(heat/photo) printing plate ready for usage in a printing process.
- As a method for continuously cast rolling a tabular plate directly from molten aluminium alloy, there can be used a method employing a cooling belt such as Hazelett method or a method employing a cooling roller such as Hunter method and 3C method. Since the Hazelett method continuously casts a thick plate, a hot rolling is subsequently conducted to make the thickness reelable. On the other hand, since the Hunter method or the 3C method makes it possible to directly cast a plate having the thickness of 10 mm or lower, a hot rolling machine is not necessary. Moreover,
JP-A-60-238001 JP-A-60-240360 - In this description basically or substantially has to be understood as at least including an angle with a horizontal plane of less than 30°, whereas an even smaller angle is preferred.
- In the present invention, the molten aluminium alloy is rapidly cooled by the continuous casting. Referring to
Figs. 1(A), 1(B), 1(C), 1(D) and 1(E) , an embodiment of the method of producing an aluminium alloy support according to the present invention will be further described. As shown inFig. 1(A) , the reference number 1 is a melt holding furnace in which an aluminium ingot is melted and retained. The molten aluminium is then fed to a twin-roller continuous casting machine 2, then wound on coiler 3. Alternatively, a continuous casting method using a cooling belt and a hot rolling may be applied as shown inFig. 1(B) . - As shown in
Fig. 1(C) , the coil wound on coiler 3 is cold rolled to a thin plate of 0.3 to 3.0 mm using cold rolling machine 4. Subsequently, as shown inFig. 1(D) , an intermediate annealing may be conducted usingheating machine 5 when necessary. As heating (annealing)machine 5, there are various types such as a batch type, a continuous annealing type, an induced heating type. The temperature is elevated at a rate of 0.5 °C/sec or more and the preferred temperature is 300 °C or more. More preferably annealing can be applied at 480°C or more. Then, the resulting thin plate is rolled again to a thickness of 0.1 to 0.5 mm using a cold rolling machine. Next, as shown inFig. 1(E) , correction is conducted using correctingmachine 6. The correction may be conducted together with a finishing rolling. - The aluminium support thus obtained is subjected to a graining treatment. When an aluminium alloy support for a printing plate is electrolytically grained, it is a common practice to carry out as a pre-treatment chemical etching with an acid or alkali for degreasing or removal of oxide films from the surface of the substrate. The electrolytic graining process, as such, is an electrolytic etching process wherein an alternating current is applied where as a counter electrode graphite or the like is used to cause electrolytic etching, thereby forming pits on the surface of the substrate to provide a grained surface.
- The above graining enhances the adhesion of a photosensitive film and improves the water retention, beneficial to printing performance, to the printing plate. Since adhesion and water retention should be provided uniformly over the whole surface of the printing plate, pits should be formed uniformly over the whole printing plate. For a printing plate provided with a photosensitive film, the grained surface should have a uniform appearance when viewed with the naked eye because the results of development after the exposure and development are evaluated by visual inspection.
- Under nonuniform electrolytic graining is to be understood, that proper surface roughness cannot be attained due to excessive etching (dissolution type) or the presence of a region remaining unetched in the electrolytic etching. In this case, a problem occurs associated with the suitability of the plate for use in printing. Specifically, the adhesion of a photosensitive film to the aluminium plate becomes poor, and, further, the water retention or corrosion resistance in nonimage areas deteriorates, which in turn leads to tinting or scumming in nonimage areas during printing.
- Nonuniform appearance of the grained surface means nonuniform color tone such as observation of streaks (a streak pattern) along the rolling direction or partial loss of gloss to give a cloudy appearance. This is caused by nonuniform chemical etching as a pre-treatment, leaving at least one region unetched or excessive etching, and electrolytic etching as an electrolytic graining treatment and a nonuniform metallic structure.
- Without being bound to theory it is believed that the nonuniform metallic structure is attributable to nonuniform aluminium crystals orientation and aluminium crystal size, coarsening and nonuniform dispersion of an intermetallic compound, and the like. Even when the nonuniformity of the metallic structure is of an extent that is not detrimental to the uniformity of electrolytic graining (including pre-treatment) necessary for printing, it often makes the appearance of the grained surface remarkably nonuniform.
- A nonuniform appearance, i.e., the presence of cloudy color shading, in the grained surface is very inconvenient to inspection of image areas after development. Specifically, the cloudy portions are present as they are in nonimage portions after development, and since they have a color tone similar to the image areas, it becomes difficult to visually judge whether or not the image areas can be satisfactorily developed.
- One of the defects which negatively influences the quality of the final printing plate is the ripple mark defect; a wave like pattern. In the prior art methods the ripple marks become visible after a sequence of surface treatments and can only clearly be observed when the final product is almost completed. However the present inventors discovered that the marks can be made visible by simply etching the surface of the support by alkaline. Aqueous solutions of sodium or potassium hydroxide are the most preferable alkali solutions and the concentration is between 5 to 40 %. Etching operation can be done by simply dipping a sample in an alkali bath. Temperature is between 15 to 35 °C, dipping time is between 1 to 10 minutes, depending on alloy, thickness, casting conditions, etc.. By the alkali etching method, the more suitable surface for planographic printing plate can be determined. This method is in principle independent from the continuous cast method used. It can be applied to the supports obtained via any of the above mentioned continuous cast methods and even for such methods as described in for example
US4523627 orWO9832559 - According to this invention, the side to be used for graining, hydrophilizing, coating, matting, etc. in order to form a good quality lithographic printing plate for supports manufactured via basically horizontal continuous casting methods, was found to be the side that is the top side during the casting process. The present inventors discovered that usage of the side that was the bottom side during the casting as surface for subsequent graining, hydrophilizing, coating, matting, etc. runs a risk of providing a non-uniform surface, in the form of ripple marks. Especially when casting operation extended over multiple coils over multiple lots, the top side during casting is much less prone to ripple mark formation, whereas the bottom side during casting quite often shows ripple marks. Usage of the top side drastically improves lot to lot fluctuation of casting in terms of ripple mark formation.
- Further, referring to the preparation conditions, the temperature in melt holding furnace 1 needs to be kept at not lower than the melting point of aluminium. The temperature in the melt holding furnace varies depending on the components of aluminium alloy. In general, it is not lower than 800 °C.
- In order to inhibit the production of oxides of molten aluminium alloy and remove alkaline metals which impair the quality of the aluminium plate, the molten aluminium alloy is subjected to a proper treatment such as inert gas purge and fluxing.
- In the present invention, a preferable constitutional range of an alloy component is as follows. In order to obtain excellent properties for a support for a planographic printing plate, the preferable Fe content in the alloy is between 0.15 and 0.50 weight %, more preferably between 0.20 and 0.35 weight %. When Fe content is less than 0.15 weight %, mechanical strength of the sheet becomes insufficient. When Fe content is more than 0.50 weight %, electrical graining structure becomes uneven. The preferable Si content is between 0.05 and 0.20 weight %, more preferably between 0.10 and 0.15 weight %. When Si content is less than 0.05 weight %, response to electrical graining becomes weak. When Si content is more than 0.20 weight %, toning characteristic of the printing plate becomes worse. The preferable Cu content is between 0.005 and 0.040 weight %, more preferably between 0.008 and 0.025 weight %. When Cu content is less than 0.005 weight %, response to electrical graining becomes weak. When Cu content is more than 0.040 weight %, resulting electrical graining structure becomes too coarse leading the printing plate having worse toning characteristic. These values have been found to be valid for at least the alloys used in the experiments as discussed hereafter.
- As the method for graining the support for planographic printing plate according to the present invention, there is used mechanical graining, chemical graining, electrochemical graining or combination thereof.
- Examples of mechanical graining methods include ball graining, wire graining, brush graining, and liquid honing. As electrochemical graining method, there is normally used AC electrolytic etching method. As electric current, there is used a normal alternating current such as sine waveform or a special alternating current such as square waveform, and the like. As a pre-treatment for the electrochemical graining, etching may be conducted with caustic soda.
- If electrochemical graining is conducted, it is preferably conducted with an alternating current in an aqueous solution mainly composed of hydrochloric acid or nitric acid. The electrochemical graining will be further described hereinafter.
- First, the aluminium support is etched with alkali. Preferred examples of alkaline agents include caustic soda, caustic potash, sodium metasilicate, sodium carbonate, sodium aluminate, sodium gluconate, etc. The concentration of the alkaline agent, the temperature of the alkaline agent and the etching time are preferably selected from 0.01 to 25%, 20 to 90 °C and 5 sec. to 5 min., respectively. The preferred etching rate is in the range of 0.1 to 15 g/m2.
- In particular, if the support contains a large amount of impurities, the etching rate is preferably in the range of 0.01 to 1 g/m2 (
JP-A-1-237197 - The pre-treatment is effected as mentioned above. In the present invention, the aluminium plate is subsequently subjected to AC electrolytic etching in an electrolyte mainly composed of hydrochloric acid or nitric acid. The frequency of the AC electrolytic current is in the range of 0.1 to 100 Hz, preferably 0.1 to 1.0 Hz or 10 to 60 Hz.
- The concentration of the etching solution is in the range of 3 to 150 g/l, preferably 5 to 50 g/l. The Content of aluminium in the etching bath is preferably in the range of not more than 50 g/l, more preferably 2 to 20 g/l. The etching bath may contain additives as necessary. However, in mass production, it is difficult to control the concentration of such an etching bath.
- The electric current density in the etching bath is preferably in the range of 5 to 100 A/dm2, more preferably 10 to 80 A/dm2. The waveform of electric current can be properly selected depending on the required quality and components of aluminium support used but may be preferably the special alternating waveform described in
U.S. Patent No. 4,087,341 (corresponding toJP-B-56-19280 JP-B-55-19191 - The aluminium plate which has been subjected to electrolytic graining is then subjected to dipping in an alkaline solution as a part of desmutting treatment to dissolve smutts away. As such an alkaline agent, there may be used caustic soda or the like. The desmutting treatment is preferably effected at a pH value of not lower than 10 and a temperature of 25 to 60°C for a dipping time as extremely short as 1 to 10 seconds.
- The aluminium plate thus etched is then dipped in a solution mainly composed of sulphuric acid. It is preferred that the sulphuric acid solution is in the concentration range of 50 to 400 g/l, and the temperature range of 20 to 70 °C. If the concentration of sulphuric acid is more than 400 g/l or the temperature of sulphuric acid is more than 70 °C, the processing bath is more liable to corrosion. Further, if the aluminium plate is etched by more than 0.4 g/m2, the printing durability may be reduced. Thus, the etching rate is preferably controlled to not more than 0.4 g/m2, more preferably not more than 0.2 g/m2.
- On the aluminium plate preferably an anodized film is formed in an amount of 0.1 to 10 g/m2, more preferably 0.3 to 5 g/m2. The anodizing conditions vary with the electrolyte used and thus are not specifically determined. In general, it is appropriate that the electrolyte concentration is in the range of 1 to 80% by weight, the electrolyte temperature is in the range of 5 to 70 °C, the electric current density is in the range of 0.5 to 60 A/dm2, the voltage is in the range of 1 to 100 V, and the electrolysis time is in the range of 1 second to 5 minutes.
- The grained aluminium plate having an anodized film thus obtained is stable and excellent in hydrophilicity itself and thus can directly form a heat- or photosensitive coat thereon. If necessary, the aluminium plate may be further subjected to a surface treatment.
- For example, a silicate layer formed by the foregoing metasilicate of alkaline metal or an undercoating layer formed by a hydrophilic polymeric compound may be formed on the aluminium plate.
- Before applying the main coating layer, an undercoating layer may be applied. The coating amount of the undercoating layer is preferably in the range of 5 to 150 mg/m2.
- A heat- and/or photosensitive coating is then formed on the aluminium plate thus treated, imagewise exposed to light, and then developed, to make a printing plate, which is then mounted in a printing machine for printing.
- The present invention will be further described in the following nonlimiting examples. Unless otherwise indicated, all parts, percents, ratios and the like are by weight.
- By the continuous casting apparatus shown in
Fig 1A , an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled. The strip was cold rolled to a thickness of 2.2 mm, then annealed at 520°C for 8 hours, and further cold rolled to form an aluminium support of a thickness of 0.278 mm. - The aluminium support was subjected to alkali etching. The material was dipped in an aqueous solution of 25 weight % sodium hydroxide at 21°C for 7 minutes, rinsed by running water, and dried. The top surface at the casting did not reveal any ripple formation.
- The top surface at the casting of the aluminium support was brush grained, etched with a 25% aqueous solution of sodium hydroxide at 50°C such that etched amount was 5 g/m2, after washing the etched plate with water, the plate was immersed in an aqueous sulphuric acid of 180 g/l at 50°C for 20 seconds to desmut the plate, and the plate was washed with water.
- Furthermore the support was electrochemically grained in 9 g/l of an aqueous nitric acid solution using the alternating (wave form ) electric current described in Japanese Patent No.
JP-B-55-19191 - An anode surface oxide coating of 2.5 g/m2 was formed on the support in a 20% sulphuric acid, and then dried. Furthermore a silicate layer was formed on the surface by dipping in an 2.5 wt% aqueous sodium metasilicate solution at 25°C.
- The thus obtained aluminium plate was examined for non-uniform parts: the plate appeared uniform in graining quality and appearance. No non-uniformity was observed.
- The following composition was coated on the aluminium plate thus-prepared in a dry coated weight of 1.3 g/m2 to provide a photosensitive layer.
Photosensitive solution: Chemical g/m2 Polyurethane consisting of 4,4'-diphenyltnethane diisocyanate / 1,6-hexamethylene diisocyanate / 2,2-bis(hydroxymethyl)-1-propionic acid / tetraethyleneglycol (80 / 20 / 20 / 80 mol %, MW = 150000) 1.01 Dodecylbenzene sulfonic acid salt of the condensate 0.15 of p-diazodiphenylamine and paraformaldehyde Phenylphosphonic acid 0.06 Victoria Pure blue 0.05 Surfactant 0.03 1-Methoxy-2- propanol 6 Methyl ethyl ketone 8 Methanol 5 - The photosensitive planographic printing plate thus-prepared was subjected to exposure for 50 seconds with a metal halide lamp of 3 kW from a distance of 1 m. through a transparent negative film, and then it was subjected to development with a developing solution of the following composition, followed by gumming in gum arabic, whereby the planographic printing plates were prepared.
Developing solution: Chemical g/l Sodium sulphite 5.0 Benzyl alcohol 30 Sodium carbonate 5.0 Sodium isopropylnaphthalenesulfonate 12.0 Purified water to make 1 lt - A printing test was carried out in a usual procedure using the planographic printing plate thus-prepared: 200.000 copies could be printed with a good quality.
- By the continuous casting apparatus shown in
Fig 1A , an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled. The strip was cold rolled to a thickness of 2.2 mm, then annealed at 520°C for 8 hours, and further cold rolled to form an aluminium support with a thickness of 0.278 mm. - The aluminium support as such was subjected to alkali etching. The support was dipped in an aqueous solution of 25 weight % sodium hydroxide at 21°C for 7 minutes, rinsed by running water, and dried. The bottom surface at the casting revealed severe ripple formation.
- This time, the side that was the bottom side during the casting process was submitted to the same steps as in Example 1. Upon examination, the plate shows an severe wave-like pattern, which renders the substrate unsuitable for further usage as a substrate for a lithographic printing plate.
- By the continuous casting apparatus shown in
Fig 1A , an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled. The strip was cold rolled to a thickness of 2.2 mm, then annealed at 380°C for 4 hours, and further cold rolled to form an aluminium support with a thickness of 0.278 mm. A similar test was repeated 10 times. - Each support formed as such was subjected to alkali etching as described in the Example 1. None of the top surfaces at the casting did reveal any ripple formation.
- The top surface at the casting of the test material was brush grained, etched with a 25% aqueous solution of sodium hydroxide at 50°C such that etched amount was 5 g/m2, after washing the etched plate with water, the plate was immersed in an aqueous sulphuric acid of 180 g/l at 50°C for 20 seconds to desmut the plate, and the plate was washed with water.
- Furthermore the support was electrochemically grained in 9 g/l of an aqueous nitric acid solution using the alternating ( wave form ) electric current in the manner as described in example 1. The quantity of electricity in the anode time became 180 coulomb/dm2.
- An anode surface oxide coating of 3.5 g/m2 was formed on the support in a 20% sulphuric acid, and then dried.
- Each aluminium plate thus obtained, was examined for non-uniform parts: all plates appeared uniform in graining quality and appearance. No non-uniformity was observed.
- The following composition was coated on the aluminium plate thus-prepared in a dry coated weight of 1.7 g/m2 to provide a photosensitive layer.
Photosensitive solution: Chemical g/m2 Ester compound of naphtoquinone-1,2-diazido-5-sulfonyl chloride and pyrogallol-acetone resin(*) 0.45 Cresol formaldehyde resin 1.10 t-Butyl phenol formaldehyde resin 0.05 Tetrahydrophtalic acid anhydride 0.09 Naphtoquinone-1,2-diazido-4-sulfonyl chloride 0.03 Ethyl violet 0.05 Megafac F-176 (fluorine containing surfactant, available from Dainippon Ink and Chemicals, Inc) 0.01 Methyl Ethyl ketone 6.0 1-Methoxy-2-propanol 4.0 (*) as disclosed in U.S. patent no. 3,635,709 (example 1) - The photosensitive planographic printing plate thus-prepared was subjected to exposure for 50 seconds with a metal halide lamp of 3 kW from a distance of 1m through a transparent positive film, and then it was subjected to development with a developing solution consisting of a 2 wt% aqueous solution of sodium silicate having a SiO2/Na2O ratio of about 1.1 and furthermore containing sodium ethylenediaminetetraacetate (0.01 g/l). The development process is followed by water rinsing and subsequent gumming in gum arabic, whereby the planographic printing plates were prepared.
- A printing test was carried out in a usual procedure using the planographic printing plate thus-prepared. 200.000 copies with high quality were obtained from all 10 trials.
- By the continuous casting apparatus shown in
Fig 1A , an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled. The strip was cold rolled to a thickness of 2.2 mm, then annealed at 380°C for 4 hours, and further cold rolled to form an aluminium support with a thickness of 0.278 mm. A similar test was repeated 10 times. - Each aluminium support formed as such was subjected to alkali etching as described in the Example 1. Five out of the ten bottom surfaces at the casting revealed strong ripple formation, and 5 revealed slight ripple formation.
- The bottom surface at the casting of each trial was treated as described in Example 2, and examined for non-uniform parts: Five out of ten plates showed a wave-like pattern, which renders the support unsuitable for further usage as a support for a lithographic printing plate. Five plates showed slight wave-like pattern, which is acceptable but not desirable.
- By the continuous casting apparatus shown in
Fig 1A , an aluminium strip (alloy AA1050) having a thickness of 5.0 mm was formed and coiled. The strip was cold rolled to a thickness of 2.2 mm, then annealed at 520°C for 8 hours, and further cold rolled to form an aluminium support with a thickness of 0.278 mm. - The aluminium support formed as such was subjected to alkali etching. The material was dipped in an aqueous solution of 25 weight % sodium hydroxide at 21°C for 7 minute, rinsed by running water, and dried. The top surface at the casting did not reveal any ripple formation. The bottom side during casting showed a clear, wave-like pattern know as ripple mark.
- The upper surface at the casting of the support was etched with a 25% aqueous solution of sodium hydroxide at 50°C such that etched amount was 5 g/m2, after washing the etched plate with water, the plate was immersed in an aqueous sulphuric acid of 180 g/l at 50°C for 20 seconds to desmut the plate, and the plate was washed with water.
- Furthermore the support was electrochemically grained in 10 g/l of an aqueous nitric acid solution using the alternating (wave form ) electric current in the manner as described in example 1. The quantity of electricity in the anode time became 280 coulomb/dm2.
- An anode surface oxide coating of 3.5 g/m2 was formed on the support in a 20% sulphuric acid, and then dried.
- Each sample of thus obtained aluminium plate was examined for non-uniform parts: all plates appeared uniform in graining quality and appearance. No non-uniformity was observed.
- The following composition was coated on the aluminium plate thus-prepared in a dry coated weight of 1.0 g/m2 to provide a heat-sensitive layer.
Chemical g/m2 m,p-Cresol novolac (m/p ratio = 6/4; weight average molecular weight: 7,500; containing 0.8 wt.% of unreacted cresol) 0.95 g Cyanine dye A (having the structure shown below) 0.025 g Megafac F177 manufactured by DAINIPPON INK & CHEMICALS, INC. 0.01 g Ethyl violet Methyl ethyl ketone 0.05 1-Methoxy-2-propanol 20.1 g 2.7 g -
- The thus obtained heat sensitive plate was imaged in a Creo Trendsetter model 3244, and developed in the developer described in Example 2. Printing plates of excellent quality with good uniform appearance were obtained.
Claims (8)
- A method of producing a planographic printing plate, comprising- casting molten aluminium substantially horizontally directly and continuously into a thin aluminium support,- determining the more suitable surface for planographic printing by determining the surface which reveals less ripple marks upon etching with an alkaline solution, wherein etching is between 1 to 10 minutes and at a temperature between 15 to 35 °C, wherein the alkaline solution has a concentration between 5 to 40 %,- roughening the aluminium support by surface treatment,- anodizing the roughened aluminium support, and- applying a heat and/or photo sensitive material to said more suitable surface.
- A method according to claim 1, wherein said casting is done by a twin roller continuous casting method.
- A method according to claim 1 or 2, wherein after the aluminium is continuously cast directly from molten aluminium into a thin aluminium support it is subjected to cold rolling, optional heat treatment and flattening to obtain an aluminium support.
- A method according to any one of the preceding claims, wherein the surface roughening of the aluminium support is at least at the side to be used for printing, in which preferably graining is used for said surface roughening.
- A method according to any one of the preceding claims, wherein the surface roughening of the aluminium support comprises etching with an alkaline solution, wherein the temperature is from 20 to 90 °C and the etching rate is 0.1 to 15 g/m2.
- A method according to any of the preceding claims, wherein an anodized film forms on said more suitable surface of the roughened aluminium support in an amount of 0.1 to 10 g/m2.
- A method according to any one of the preceding claims, wherein an aluminium alloy is used containing between 0.15 and 0.50 weight % Fe and/or 0.05 and 0.20 weight % Si and/or 0.005 and 0.040 weight % Cu.
- A method according to any one of the preceding claims, wherein an aluminium alloy is used containing between 0.20 and 0.35 weight% Fe and/or 0.10 and 0.15 weight % Si and/or 0.008 and 0.025 weight % Cu.
Priority Applications (1)
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EP04076742A EP1486348B1 (en) | 2003-06-12 | 2004-06-11 | Method of producing a planographic printing plate |
Applications Claiming Priority (3)
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EP03076834A EP1486347A1 (en) | 2003-06-12 | 2003-06-12 | Aluminium alloy substrate for lithographic printing plate and method for producing the same |
EP03076834 | 2003-06-12 | ||
EP04076742A EP1486348B1 (en) | 2003-06-12 | 2004-06-11 | Method of producing a planographic printing plate |
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EP1486348A2 EP1486348A2 (en) | 2004-12-15 |
EP1486348A3 EP1486348A3 (en) | 2005-08-31 |
EP1486348B1 true EP1486348B1 (en) | 2013-01-02 |
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EP04076742A Expired - Lifetime EP1486348B1 (en) | 2003-06-12 | 2004-06-11 | Method of producing a planographic printing plate |
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EP1543899A3 (en) * | 2003-12-17 | 2005-12-21 | Fuji Photo Film B.V. | Aluminium alloy substrate for digitally imageable lithographic printing plate and process for producing the same |
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JP2767711B2 (en) | 1989-08-22 | 1998-06-18 | 富士写真フイルム株式会社 | Method for producing a lithographic printing plate support |
JP3054719B2 (en) | 1991-12-02 | 2000-06-19 | 富士写真フイルム株式会社 | Method for producing a lithographic printing plate support |
EP0603476B1 (en) * | 1992-11-20 | 1998-08-12 | Fuji Photo Film Co., Ltd. | Support for a planographic printing plate and method for producing same |
JP3454578B2 (en) * | 1993-08-31 | 2003-10-06 | 日本軽金属株式会社 | Aluminum alloy base plate for lithographic printing plate and method for producing the same |
JP3290274B2 (en) * | 1993-11-15 | 2002-06-10 | 富士写真フイルム株式会社 | Method for producing lithographic printing plate support |
JPH10258340A (en) * | 1997-03-14 | 1998-09-29 | Fuji Photo Film Co Ltd | Aluminum support body for lithographic press plate, and its manufacture |
DE19900427A1 (en) * | 1999-01-08 | 2000-07-13 | Sms Demag Ag | Method and device for descaling a surface of a cast strand having oscillation marks from a continuous casting installation |
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