US3617266A - Process for preparing a planographic printing form - Google Patents
Process for preparing a planographic printing form Download PDFInfo
- Publication number
- US3617266A US3617266A US710723A US3617266DA US3617266A US 3617266 A US3617266 A US 3617266A US 710723 A US710723 A US 710723A US 3617266D A US3617266D A US 3617266DA US 3617266 A US3617266 A US 3617266A
- Authority
- US
- United States
- Prior art keywords
- planographic printing
- preparing
- printing plate
- plate according
- polymeric compound
- 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
- 238000007639 printing Methods 0.000 title claims abstract description 34
- 238000004519 manufacturing process Methods 0.000 title claims description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- 229920000642 polymer Polymers 0.000 claims abstract description 17
- 125000003277 amino group Chemical class 0.000 claims abstract description 13
- 150000003839 salts Chemical group 0.000 claims abstract description 8
- 229920000768 polyamine Polymers 0.000 claims abstract description 7
- 239000007788 liquid Substances 0.000 claims description 23
- 239000000084 colloidal system Substances 0.000 claims description 5
- 239000012071 phase Substances 0.000 claims description 4
- 238000013016 damping Methods 0.000 claims description 3
- 239000008346 aqueous phase Substances 0.000 claims description 2
- YAGKRVSRTSUGEY-UHFFFAOYSA-N ferricyanide Chemical compound [Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] YAGKRVSRTSUGEY-UHFFFAOYSA-N 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims description 2
- 230000002209 hydrophobic effect Effects 0.000 abstract description 12
- 239000007864 aqueous solution Substances 0.000 abstract description 7
- 125000001931 aliphatic group Chemical group 0.000 abstract description 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 239000001257 hydrogen Substances 0.000 abstract description 2
- 229920002554 vinyl polymer Chemical class 0.000 abstract description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 14
- 238000000034 method Methods 0.000 description 11
- 239000011230 binding agent Substances 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000011787 zinc oxide Substances 0.000 description 7
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 3
- 235000010443 alginic acid Nutrition 0.000 description 3
- 229920000615 alginic acid Polymers 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- -1 caseinates Substances 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 235000011167 hydrochloric acid Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- 239000000467 phytic acid Substances 0.000 description 2
- 235000002949 phytic acid Nutrition 0.000 description 2
- 229940068041 phytic acid Drugs 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- KNIUHBNRWZGIQQ-UHFFFAOYSA-N 7-diethoxyphosphinothioyloxy-4-methylchromen-2-one Chemical compound CC1=CC(=O)OC2=CC(OP(=S)(OCC)OCC)=CC=C21 KNIUHBNRWZGIQQ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 244000165918 Eucalyptus papuana Species 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- PFRUBEOIWWEFOL-UHFFFAOYSA-N [N].[S] Chemical compound [N].[S] PFRUBEOIWWEFOL-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000000728 ammonium alginate Substances 0.000 description 1
- 235000010407 ammonium alginate Nutrition 0.000 description 1
- KPGABFJTMYCRHJ-YZOKENDUSA-N ammonium alginate Chemical compound [NH4+].[NH4+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O KPGABFJTMYCRHJ-YZOKENDUSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 229940126543 compound 14 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- LRBQNJMCXXYXIU-QWKBTXIPSA-N gallotannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@H]2[C@@H]([C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-QWKBTXIPSA-N 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 230000005660 hydrophilic surface Effects 0.000 description 1
- 229920001600 hydrophobic polymer Polymers 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229940005642 polystyrene sulfonic acid Drugs 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 229940024463 silicone emollient and protective product Drugs 0.000 description 1
- 239000000264 sodium ferrocyanide Substances 0.000 description 1
- GTSHREYGKSITGK-UHFFFAOYSA-N sodium ferrocyanide Chemical compound [Na+].[Na+].[Na+].[Na+].[Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] GTSHREYGKSITGK-UHFFFAOYSA-N 0.000 description 1
- 235000012247 sodium ferrocyanide Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- GXORKTXNRMWBQR-UHFFFAOYSA-L zinc tridecyl phosphate Chemical compound P(=O)(OCCCCCCCCCCCCC)([O-])[O-].[Zn+2] GXORKTXNRMWBQR-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/26—Electrographic processes using a charge pattern for the production of printing plates for non-xerographic printing processes
- G03G13/28—Planographic printing plates
Definitions
- a planographic printing plate prepared by electrostatic exposure and development and carrying a hydrophobic deposit from such development in the image areas thereof is hydrophilized by treatment with an aqueous solution containing a polymeric compound having in the recurring units thereof an amino salt and/or quaternary salt group the polymer compound being free of long chain hydrocarbon groups.
- Preferred hydrophilizing compounds are polyamines having aliphatic linkages between the amino groups and polyvinyl compounds having hydrogen-containing heterocyclic side groups.
- PROCESS FOR PREPARING A PLANOGRAPHIC PRINTING FORM This invention relates to a process for preparing planographic printing plate and to the printing plate obtained therewith.
- Planographic printing is based on the physical property of repellcnce of greasy materials for water.
- the printing surface which is substantially flat, contains the pattern of the image to be printed in terms of a differentiation in water repellency.
- ln 1 the ordinary lithographic or planographic printing processes a printing plate is prepared by afi'ixing to a water-attractive, hydrophilic surface, a water repellent, hydrophobic image,
- the electrostatic image is rendered visible by applying a developer powder; which is held electrostatically to the charged areas of the sheet.
- the powder image preferably composed of hydrophobic fusible powder particles may be fixed by heating.
- the difference in hydrophobicity between the developed image parts and the noncovered areas of the recording layer is not high enough for high quality planographic printing and has to be increased. Therefor it has been. proposed to treat the recording layer chemically in the undeveloped areas in order to make said areas highly water- I receptive.
- a photoconductive insulating recording layer comprising an electrically insulating binder having suspended therein an inorganic photoconductive substance that can provide zinc ions, such as photoconductive zinc oxide, can be provided with improved hydrophility by treating it with a polyamino compound comprising at least two nonaromatic amino groups, e.g. aliphatic, cycloaliphatic, cycloor heterocyclic amino groups without aromatic character, at least one of these amino groups being present in salt form or quatemized form.
- a polyamino compound comprising at least two nonaromatic amino groups, e.g. aliphatic, cycloaliphatic, cycloor heterocyclic amino groups without aromatic character, at least one of these amino groups being present in salt form or quatemized form.
- the aliphatic or cycloaliphatic chains of the nonaromatic amine groups may consist entirely of chains of carbon atoms, or the chains may contain carbon atoms interspaced with oxygen, sulfur nitrogen or phosphorus atoms or combinations thereof.
- the chains may contain ester, amide, ether, imidazole, or urethane linkages, or their thio-equivalents.
- Use is preferably made of a polymeric compound containing one or more aliphatic amino groups in the recurring units e.g. a polyalkyleneimine compound wherein part of the amino groups or all of them are transformed into a salt form or a quatemized form.
- a polymeric compound containing one or more aliphatic amino groups in the recurring units e.g. a polyalkyleneimine compound wherein part of the amino groups or all of them are transformed into a salt form or a quatemized form.
- R is a C,-C,,alltyl group
- m is an integer from 2 to 50.
- n is at least 2.
- the polyamino compounds for use according to the present invention are preferably dissolved in an aqueous liquid in a concentration of 0.1 to 20 percent by weight calculated on the total weight ofthe liquid.
- polyamino compounds comprising amino group(s) in neutralized or quaternized form are preferably used in com bination with water-soluble ferricyanides and/or water-soluble ferrocyanides since the sparingly water-soluble hydrophilic zinc salts formed therewith have a relatively high adsorption power for cationic compounds and therefore have a mordanting efi'ect on said neutralized or quaternized polyamino compounds.
- a printing plate containing in the hydrophilized portions a coprecipitate of zinc ferriand/or zinc ferrocyanide and a neutralized or quaternized polyamine has a high resistance to wear, which is important for long run printing. That resistance to wear can still be increased with hydrophilic colloids which may be applied simultaneously with or after the treatment with said polyamines.
- Suitable hydrophilic colloids for that purpose are e.g. gum arabic, alginic acid, water-soluble alginates e.g. ammonium alginate, caseinates, gelatin, polyacrylic acid esters, polystyrene sulfonic acid, polyvinyl alcohol, and 5 carboxymethylcellulose.
- a treatment with hydrophilic precipitating or hardening agents for these colloids has proved to be advantageous. So, use can be made of formaldehyde as protein hardener and heavy metal salts forming a precipitate e.g. with alginates.
- the pH of the hydrophilizing liquid is preferably below 7 and more preferably within the range of 3 to 6.
- water-soluble mineral and/or organic acids can be used e.g. orthophosphoric acid, nitric acid, sulfuric acid, hydrochloric acid, boric acid, acetic acid, citric acid, tartaric acid, tannic acid and lactic acid.
- the hydrophilizing action of the hydrophilizing agent may be improved by a pretreatment of the developed and fixed recording layer with a softening or swelling agent for thebinder occasionally in combination with a wetting agent improving the penetrating power of the hydrophilizing agent in the recordin gTayerT In this way much more zinc oxide grains are reached by thehydrophilizing agent and hydrophilized.
- swelling agents preferably water-miscible compounds such as acetone and methyl ethyl ketone are used.
- the electrophotographic recording layer is rendered water-receptive at the areas to be hydrophilized after the printing master has been mounted on the press, thus obviating any separate immersion treatment.
- the hydrophilizing treatment of said layer may be carried out by means of an absorbent pad impregnated with an aqueous solution containing the partly or wholly neutralized or quaternized polyamine.
- Electrophotographic recording materials which are especially suited to be used in the preparation of a planographic printing plate, are described e.g. in the published Dutch Pat. applications 6,608,814 and 6,608,815.
- Any known process for forming the electrostatic latent image and hydrophobic image may be applied.
- the hydrophobic image is formed by the consecutive steps of producing an electrostatic image on a photoconductive zinc oxide/hydrophobic binder layer by integrally electrostatically charging that layer, subsequently image-wise exposing and developing the latter with a hydrophobic developer powder, which is fixed to the recording layer e.g. by heating.
- the powder image can be formed by the known dry carrier-toner development" or by a liquid development based on electrophoresis wherein charged hydrophobic particles are attracted from an electrically insulating liquid to be charged areas of the recording layer.
- Such development technique is described eg in the U.K. Pat. specification 755,486.
- an electrostatic latent image can also be developed by a selective deposit of an aqueous developing composition.
- That composition can e.g. contain a dispersed hydrophobic polymer, which on drying the liquid image is image-wise left and forms a hydrophobic pattern.
- polyamines applied according to the present invention can be used in combination with other hydrophilizing compounds.
- EXAMPLE 1 A layer of photoconductive material consisting of photoconductive zinc oxide dispersed in an insulating binder (3 parts by weight of zinc oxide to 1 part by weight or resin binder) was coated on a sheet of aluminum foil laminated to a paper support.
- the resin binder contained on a weight basis of styrene-butadiene copolymer (80/20), 20% of silicone resin (Silicone Resin SR-82 supplied by General Electric Silicone Products Department Waterford, N.Y., U.S.A.).
- the recording layer was charged with a negative corona with a tension of 6000 v. on the corona wires and exposed through a graphic original. Development was carried out by using the magnetic brush technique with iron particles as carrier and gilsonite as fusible toner.
- the powder image was fixed to the layer by heating for seconds at C.
- a cotton pad was impregnated with a solution containing the following ingredients:
- the plate was rubbed softly with the cotton pad while on the press.
- the quality of prints was very good.
- EXAMPLE 6 A layer of photoconductive material consisting of photoconductive zinc oxide dispersed in an insulating binder (6 parts by weight of zinc oxide to l part by weight of binder) was coated on a flexible aluminum foil.
- the binder was prepared from a mixture of EPOK X-l 772 (ammoniacal alkyd resin salt marketed as a 66 to 68 percent (by weight) aqueous solution by British Resin Products Ltd.) and EPOK W-980l (a 72 to 75 percent aqueous solution ofa melamine-formaldehyde resin marketed by British Resin Products).
- EPOK X-l 772 ammoniacal alkyd resin salt marketed as a 66 to 68 percent (by weight) aqueous solution by British Resin Products Ltd.
- EPOK W-980l a 72 to 75 percent aqueous solution ofa melamine-formaldehyde resin marketed by British Resin Products
- the cured recording layer was charged with a negative corona with a tension of 6000 v. on the corona-wires and exposed to a line-copy.
- the electrostatic image was electrophoretically developed by means of an electrophoretic developer obtained by diluting the hereinafter described concentrated developer composition in a volume ratio of l5/l000 with the hydrocarbon solvent SHELLSOL T (trade name) carbon black (average particle size p.)
- SHELLSOL T (trade name) 750 cc.
- the resin binder solution was prepared by heating 500 g. of ALKYDAL L 67 [trade name by Konverkusen, West Germany, for a linseed oil (67. percent by weight) modified alkyd resin] and 500 cc. of white spirit containing l 1 percent by weight of aromatic compounds at 60 C. till a clear solution was obtained, and subsequent cooling.
- ALKYDAL L 67 trade name by Konverkusen, West Germany
- SOLIDOGEN FFL (trade name) 5 cc. sodium ferrocyanide l g. sodium sulfite (antioxidant) 2.5 g.
- Example 7 Example 6 was repeated, with the proviso, however, that the hydrophilizing liquid was acidified till pH 3 by means of tartaric acid, phosphoric acid, citric acid, phytic acid, or oxalic acid.
- Example I was repeated with the proviso, however, that the hydrophilizing liquid was acidified till pH 6 and that it contained 5 percent by weight of the quaternized polyamino compound No. 6 of the table.
- the hydrophilization obtained was equivalent to that according to the procedure of example I. Results of slightly inferior quality were obtained by using the compounds Nos. 7, 8 and 9 in the same concentration at pH values of 6, 2 and 6 respectively.
- a process for preparing a planographic printing plate comprising the steps of forming a latent electrostatic image on a photoconductive insulating recording layer containing an inorganic photoconductive substance, which can provide zinc ions, and developing said image with a toner forming an image-wise hydrophobic deposit on said recording layer, the improvement of treating the portions of the recording layer whichare not covered with said hydrophobic deposit with an aqueous hydrophilizing solution containing a a water-soluble polyamino compound comprising at least two nonaromatic amino groups with each adjacent pair of such amino groups being connected by an aliphatic linkage'including a hydrocarboifchain (fit leis: two but not more than six carbon atoms, said compounds containing not more than six carbon atoms in a continuous carbon chain, at least part of the amino groups in said compound being in amine salt or quaternized salt form.
- polyamino compound is a. member of the group consisting of:
- n is an integer from 2 to 50;
- R is a. C -C alkyl group; and a: is an integer from 2 to 50;
- n is at least 2;
- n is at least 2;
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Printing Plates And Materials Therefor (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB00475/67A GB1192602A (en) | 1967-03-06 | 1967-03-06 | Process for Preparing a Planographic Printing Plate |
GB10477/67A GB1198123A (en) | 1967-03-06 | 1967-03-06 | Process for Preparing a Planographic Printing Master |
GB10476/67A GB1198122A (en) | 1967-03-06 | 1967-03-06 | Process for Preparing a Planographic Printing Form |
Publications (1)
Publication Number | Publication Date |
---|---|
US3617266A true US3617266A (en) | 1971-11-02 |
Family
ID=27256529
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US710723A Expired - Lifetime US3617266A (en) | 1967-03-06 | 1968-03-06 | Process for preparing a planographic printing form |
US710729A Expired - Lifetime US3573041A (en) | 1967-03-06 | 1968-03-06 | Process for preparing a planographic printing plate |
US710730A Expired - Lifetime US3592640A (en) | 1967-03-06 | 1968-03-06 | Process for preparing a planographic printing master |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US710729A Expired - Lifetime US3573041A (en) | 1967-03-06 | 1968-03-06 | Process for preparing a planographic printing plate |
US710730A Expired - Lifetime US3592640A (en) | 1967-03-06 | 1968-03-06 | Process for preparing a planographic printing master |
Country Status (7)
Country | Link |
---|---|
US (3) | US3617266A (enrdf_load_stackoverflow) |
BE (1) | BE711704A (enrdf_load_stackoverflow) |
CH (1) | CH500512A (enrdf_load_stackoverflow) |
DE (1) | DE1622950A1 (enrdf_load_stackoverflow) |
FR (1) | FR1558045A (enrdf_load_stackoverflow) |
GB (3) | GB1198122A (enrdf_load_stackoverflow) |
NL (1) | NL6803164A (enrdf_load_stackoverflow) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3946671A (en) * | 1972-09-28 | 1976-03-30 | The Commonwealth Of Australia | Electrostatic offset printing |
US3948827A (en) * | 1973-10-26 | 1976-04-06 | Dai Nippon Printing Company Limited | Dry planographic printing ink composition |
US3970455A (en) * | 1973-06-04 | 1976-07-20 | Itek Corporation | Electrostatic lithographic printing process utilizing hydrophilizing composition |
US4058470A (en) * | 1975-10-24 | 1977-11-15 | A. B. Dick Company | Liquid developer composition for lithographic masters |
EP0135031A1 (en) * | 1983-07-19 | 1985-03-27 | Tomoegawa Paper Co. Ltd. | Desensitizing solution for use in offset printing |
US5525458A (en) * | 1993-09-02 | 1996-06-11 | Tomoegawa Paper Co., Ltd. | Desensitizing solution for lithographic platemaking |
US5565290A (en) * | 1991-07-30 | 1996-10-15 | Fuji Photo Film Co., Ltd. | Desensitizing solution for offset printing |
US5681686A (en) * | 1993-04-20 | 1997-10-28 | Iwatsu Electric Co., Ltd | Desensitizing solution for offset printing |
JP3222667B2 (ja) | 1993-11-16 | 2001-10-29 | 株式会社巴川製紙所 | 平版印刷用不感脂化処理液 |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3807305A (en) * | 1968-07-15 | 1974-04-30 | Itek Corp | Metal photographic plate comprising a silver halide process |
US3807304A (en) * | 1968-07-15 | 1974-04-30 | Itek Corp | Photographic process for producing coherent metallic image bonded to a roughened support and products produced thereby |
US4053319A (en) * | 1973-06-04 | 1977-10-11 | Itek Corporation | Hydrophilizing composition for lithographic printing plates |
NL7606078A (nl) * | 1975-06-12 | 1976-12-14 | Dow Chemical Co | Werkwijze voor het bereiden van een bevochti- gingsoplossing voor lithografische drukken. |
US4070969A (en) * | 1976-07-16 | 1978-01-31 | Minnesota Mining And Manufacturing Company | Method for strengthening lithographic printing plate images |
US4043811A (en) * | 1976-07-29 | 1977-08-23 | Addressograph Multigraph Corporation | Conversion solutions for planographic masters |
DE2934897C1 (de) * | 1978-02-06 | 1984-09-20 | Napp Systems (USA), Inc., San Marcos, Calif. | Desensibilisierungsloesung fuer fotoempfindliche Diazodruckplatten |
GB8501868D0 (en) * | 1985-01-25 | 1985-02-27 | Byrne P | Board game |
JPS6277994A (ja) * | 1985-10-01 | 1987-04-10 | Nikken Kagaku Kenkyusho:Kk | オフセツト印刷用電子写真版の不感脂化処理液 |
JPH01133795A (ja) * | 1987-11-19 | 1989-05-25 | Nikken Kagaku Kenkyusho:Kk | オフセツト印刷用電子写真版の不感脂化処理液 |
JP2622753B2 (ja) * | 1988-06-27 | 1997-06-18 | 石原産業株式会社 | オフセット印刷マスターの作成方法 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2023669A (en) * | 1933-01-06 | 1935-12-10 | Art of printing | |
US3106158A (en) * | 1962-01-22 | 1963-10-08 | Rca Corp | Method of preparing lithographic printing plates |
US3211686A (en) * | 1959-06-18 | 1965-10-12 | Plastic Coating Corp | Aqueous composition for prewetting a master carrying an image prepared by electrophotographic reproduction containing polyacrylic acid |
US3230081A (en) * | 1959-08-04 | 1966-01-18 | Azoplate Corp | Process for the preparation of printing plates utilizing electrostatic image formation techniques |
US3245784A (en) * | 1961-10-16 | 1966-04-12 | Minnesota Mining & Mfg | Lithographic master and process of preparation |
US3309940A (en) * | 1963-11-27 | 1967-03-21 | Int Standard Electric Corp | Detention mechanism for rotary switches, particularly stepping switches |
-
1967
- 1967-03-06 GB GB10476/67A patent/GB1198122A/en not_active Expired
- 1967-03-06 GB GB00475/67A patent/GB1192602A/en not_active Expired
- 1967-03-06 GB GB10477/67A patent/GB1198123A/en not_active Expired
-
1968
- 1968-03-02 DE DE19681622950 patent/DE1622950A1/de active Pending
- 1968-03-05 FR FR1558045D patent/FR1558045A/fr not_active Expired
- 1968-03-05 CH CH323268A patent/CH500512A/de not_active IP Right Cessation
- 1968-03-06 BE BE711704D patent/BE711704A/xx unknown
- 1968-03-06 NL NL6803164A patent/NL6803164A/xx unknown
- 1968-03-06 US US710723A patent/US3617266A/en not_active Expired - Lifetime
- 1968-03-06 US US710729A patent/US3573041A/en not_active Expired - Lifetime
- 1968-03-06 US US710730A patent/US3592640A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2023669A (en) * | 1933-01-06 | 1935-12-10 | Art of printing | |
US3211686A (en) * | 1959-06-18 | 1965-10-12 | Plastic Coating Corp | Aqueous composition for prewetting a master carrying an image prepared by electrophotographic reproduction containing polyacrylic acid |
US3230081A (en) * | 1959-08-04 | 1966-01-18 | Azoplate Corp | Process for the preparation of printing plates utilizing electrostatic image formation techniques |
US3245784A (en) * | 1961-10-16 | 1966-04-12 | Minnesota Mining & Mfg | Lithographic master and process of preparation |
US3106158A (en) * | 1962-01-22 | 1963-10-08 | Rca Corp | Method of preparing lithographic printing plates |
US3309940A (en) * | 1963-11-27 | 1967-03-21 | Int Standard Electric Corp | Detention mechanism for rotary switches, particularly stepping switches |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3946671A (en) * | 1972-09-28 | 1976-03-30 | The Commonwealth Of Australia | Electrostatic offset printing |
US3970455A (en) * | 1973-06-04 | 1976-07-20 | Itek Corporation | Electrostatic lithographic printing process utilizing hydrophilizing composition |
US3948827A (en) * | 1973-10-26 | 1976-04-06 | Dai Nippon Printing Company Limited | Dry planographic printing ink composition |
US4058470A (en) * | 1975-10-24 | 1977-11-15 | A. B. Dick Company | Liquid developer composition for lithographic masters |
EP0135031A1 (en) * | 1983-07-19 | 1985-03-27 | Tomoegawa Paper Co. Ltd. | Desensitizing solution for use in offset printing |
US5565290A (en) * | 1991-07-30 | 1996-10-15 | Fuji Photo Film Co., Ltd. | Desensitizing solution for offset printing |
US5681686A (en) * | 1993-04-20 | 1997-10-28 | Iwatsu Electric Co., Ltd | Desensitizing solution for offset printing |
US5525458A (en) * | 1993-09-02 | 1996-06-11 | Tomoegawa Paper Co., Ltd. | Desensitizing solution for lithographic platemaking |
JP3222667B2 (ja) | 1993-11-16 | 2001-10-29 | 株式会社巴川製紙所 | 平版印刷用不感脂化処理液 |
Also Published As
Publication number | Publication date |
---|---|
DE1622950A1 (de) | 1971-01-14 |
US3573041A (en) | 1971-03-30 |
CH500512A (de) | 1970-12-15 |
GB1198122A (en) | 1970-07-08 |
FR1558045A (enrdf_load_stackoverflow) | 1969-02-21 |
GB1192602A (en) | 1970-05-20 |
US3592640A (en) | 1971-07-13 |
GB1198123A (en) | 1970-07-08 |
NL6803164A (enrdf_load_stackoverflow) | 1968-05-27 |
BE711704A (enrdf_load_stackoverflow) | 1968-09-06 |
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