EP1295717B1 - Wärmeempfindlicher positiv arbeitender Flachdruckplattenvorläufer - Google Patents

Wärmeempfindlicher positiv arbeitender Flachdruckplattenvorläufer Download PDF

Info

Publication number
EP1295717B1
EP1295717B1 EP02102309A EP02102309A EP1295717B1 EP 1295717 B1 EP1295717 B1 EP 1295717B1 EP 02102309 A EP02102309 A EP 02102309A EP 02102309 A EP02102309 A EP 02102309A EP 1295717 B1 EP1295717 B1 EP 1295717B1
Authority
EP
European Patent Office
Prior art keywords
developer
optionally substituted
printing plate
coating
plate precursor
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 - Fee Related
Application number
EP02102309A
Other languages
English (en)
French (fr)
Other versions
EP1295717A3 (de
EP1295717A2 (de
Inventor
Marc AGFA-Gevaert Van Damme
Joan AGFA-GEVAERT Vermeersch
Geert AGFA-GEVAERT Deroover
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Agfa NV
Original Assignee
Agfa Graphics NV
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Agfa Graphics NV filed Critical Agfa Graphics NV
Priority to EP02102309A priority Critical patent/EP1295717B1/de
Publication of EP1295717A2 publication Critical patent/EP1295717A2/de
Publication of EP1295717A3 publication Critical patent/EP1295717A3/de
Application granted granted Critical
Publication of EP1295717B1 publication Critical patent/EP1295717B1/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C1/00—Forme preparation
    • B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
    • B41C1/1008—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials
    • B41C1/1016—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials characterised by structural details, e.g. protective layers, backcoat layers or several imaging layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C1/00—Forme preparation
    • B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
    • B41C1/1008—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials
    • 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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/02—Positive working, i.e. the exposed (imaged) areas are removed
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/06—Developable by an alkaline solution
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/22—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation characterised by organic non-macromolecular additives, e.g. dyes, UV-absorbers, plasticisers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/24—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation characterised by a macromolecular compound or binder obtained by reactions involving carbon-to-carbon unsaturated bonds, e.g. acrylics, vinyl polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/26—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation characterised by a macromolecular compound or binder obtained by reactions not involving carbon-to-carbon unsaturated bonds
    • B41C2210/262—Phenolic condensation polymers, e.g. novolacs, resols

Definitions

  • the present invention relates to a heat-sensitive positive-working lithographic printing plate precursor that requires aqueous alkaline processing.
  • Lithographic printing presses use a so-called printing master such as a printing plate which is mounted on a cylinder of the printing press.
  • the master carries a lithographic image on its surface and a print is obtained by applying ink to said image and then transferring the ink from the master onto a receiver material, which is typically paper.
  • ink as well as an aqueous fountain solution also called dampening liquid
  • the lithographic image which consists of oleophilic (or hydrophobic, i.e. ink-accepting, water-repelling) areas as well as hydrophilic (or oleophobic, i.e. water-accepting, ink-repelling) areas.
  • so-called driographic printing the lithographic image consists of ink-accepting and ink-abhesive (ink-repelling) areas and during driographic printing, only ink is supplied to the master.
  • Printing masters are generally obtained by the so-called computer-to-film method wherein various pre-press steps such as typeface selection, scanning, color separation, screening, trapping, layout and imposition are accomplished digitally and each color selection is transferred to graphic arts film using an image-setter.
  • the film can be used as a mask for the exposure of an imaging material called plate precursor and after plate processing, a printing plate is obtained which can be used as a master.
  • a typical printing plate precursor for computer-to-film methods comprise a hydrophilic support and an image-recording layer of a photosensitive polymer layers which include UV-sensitive diazo compounds, dichromate-sensitized hydrophilic colloids and a large variety of synthetic photopolymers. Particularly diazo-sensitized systems are widely used.
  • Upon image-wise exposure typically by means of a film mask in a UV contact frame, the exposed image areas become insoluble and the unexposed areas remain soluble in an aqueous alkaline developer.
  • the plate is then processed with the developer to remove the diazonium salt or diazo resin in the unexposed areas.
  • the exposed areas define the image areas (printing areas) of the printing master, and such printing plate precursors are therefore called 'negative-working'.
  • positive-working materials wherein the exposed areas define the non-printing areas, are known, e.g. plates having a novolac/naphtoquinone-diazide coating which dissolves in the developer only at exposed areas.
  • thermoplastic polymer latex In addition to the above photosensitive materials, also heat-sensitive printing plate precursors have become very popular. Such thermal materials offer the advantage of daylight-stability and are especially used in the so-called computer-to-plate method wherein the plate precursor is directly exposed, i.e. without the use of a film mask. The material is exposed to heat or to infrared light and the generated heat triggers a (physico-)chemical process, such as ablation, polymerization, insolubilization by cross-linking of a polymer, decomposition, or particle coagulation of a thermoplastic polymer latex.
  • a (physico-)chemical process such as ablation, polymerization, insolubilization by cross-linking of a polymer, decomposition, or particle coagulation of a thermoplastic polymer latex.
  • WO97/39894 and EP-A 823 327 describe positive-working heat-sensitive materials comprising a hydrophilic support and a oleophilic coating provided thereon.
  • the coating comprises a phenolic resin and a dissolution inhibitor, i.e. a compound which reduces the solubility of the phenolic resin in an aqueous alkaline developer.
  • the interaction between the inhibitor and the phenolic resin is disrupted by exposure to heat or infrared light and, as a result, the exposed areas of the coating dissolve faster in the developer than the non-exposed areas and a lithographic image consisting of hydrophilic (exposed) and oleophilic (non-exposed) areas is obtained.
  • EP-A 864 420 and EP-A 950 517 disclose the use of developer resistance means such as polysiloxane compounds which are capable of preventing the aqueous alkaline developer from penetrating into the phenolic resin layer.
  • developer resistance means such as polysiloxane compounds which are capable of preventing the aqueous alkaline developer from penetrating into the phenolic resin layer.
  • the increased developer resistance thus obtained can be reduced by exposure to heat or infrared light and upon subsequent immersion in the developer, a positive lithographic image is obtained.
  • the coating of the known printing plates contain a colorant, also called contrast dye or indicator dye, in order to provide a visible image after image-wise exposure and development.
  • a colorant also called contrast dye or indicator dye
  • Such colorants remain in the coating at printing areas and are removed, together with the coating, at non-printing areas.
  • Most of such prior art materials are characterized by a low sensitivity and therefore require a high power during exposure.
  • the colorants that are used as indicator dyes in the prior art materials, are typically organic molecules containing quaternary nitrogen atoms, or carbonyl (-CO-), sulfinyl (-SO-) or sulfonyl (-SO 2 -) groups. Such groups have a dissolution inhibiting effect, probably due to hydrogen bridge formation with the binder(s) present in the coating such as phenolic resins.
  • Known examples of such inhibiting dyes are the amino-substituted tri- or diarylmethane dyes, e.g. crystal violet, methyl violet, violet pure blue, auramine and malachite green.
  • the colorants which are used in the prior art materials can be replaced by alternatives that are non-inhibiting.
  • Such colorants provide a higher sensitivity, even if the absorption efficiency at the wavelength of the image-wise exposure is not affected thereby.
  • the lithographic printing plate precursor of the present invention contains a hydrophilic support and a coating comprising an oleophilic layer provided thereon.
  • the printing plate precursor is positive-working, i.e. after exposure and development the exposed areas of the oleophilic layer are removed from the support and define hydrophilic (non-printing) areas, whereas the unexposed layer is not removed from the support and defines an oleophilic (printing) area.
  • the support has a hydrophilic surface or is provided with a hydrophilic layer.
  • the support may be a sheet-like material such as a plate or it may be a cylindrical element such as a sleeve which can be slid around a print cylinder of a printing press.
  • the support is a metal support such as aluminum or stainless steel.
  • a particularly preferred lithographic support is an electrochemically grained and anodized aluminum support.
  • the anodized aluminum support may be treated to improve the hydrophilic properties of its surface.
  • the aluminum support may be silicated by treating its surface with a sodium silicate solution at elevated temperature, e.g. 95°C.
  • a phosphate treatment may be applied which involves treating the aluminum oxide surface with a phosphate solution that may further contain an inorganic fluoride.
  • the aluminum oxide surface may be rinsed with a citric acid or citrate solution. This treatment may be carried out at room temperature or may be carried out at a slightly elevated temperature of about 30 to 50°C.
  • a further interesting treatment involves rinsing the aluminum oxide surface with a bicarbonate solution.
  • the aluminum oxide surface may be treated with polyvinylphosphonic acid, polyvinylmethylphosphonic acid, phosphoric acid esters of polyvinyl alcohol, polyvinylsulfonic acid, polyvinylbenzenesulfonic acid, sulfuric acid esters of polyvinyl alcohol, and acetals of polyvinyl alcohols formed by reaction with a sulfonated aliphatic aldehyde It is further evident that one or more of these post treatments may be carried out alone or in combination.
  • the support can also be a flexible support, which is provided with a hydrophilic layer, hereinafter called 'base layer'.
  • the flexible support is e.g. paper, plastic film, thin aluminum or a laminate thereof.
  • Preferred examples of plastic film are polyethylene terephthalate film, polyethylene naphthalate film, cellulose acetate film, polystyrene film, polycarbonate film, etc.
  • the plastic film support may be opaque or transparent.
  • the base layer is preferably a cross-linked hydrophilic layer obtained from a hydrophilic binder cross-linked with a hardening agent such as formaldehyde, glyoxal, polyisocyanate or a hydrolyzed tetra-alkylorthosilicate.
  • a hardening agent such as formaldehyde, glyoxal, polyisocyanate or a hydrolyzed tetra-alkylorthosilicate.
  • the thickness of the hydrophilic base layer may vary in the range of 0.2 to 25 ⁇ m and is preferably 1 to 10 ⁇ m.
  • the hydrophilic binder for use in the base layer is e.g. a hydrophilic (co)polymer such as homopolymers and copolymers of vinyl alcohol, acrylamide, methylol acrylamide, methylol methacrylamide, acrylate acid, methacrylate acid, hydroxyethyl acrylate, hydroxyethyl methacrylate or maleic anhydride/vinylmethylether copolymers.
  • the hydrophilicity of the (co)polymer or (co)polymer mixture used is preferably the same as or higher than the hydrophilicity of polyvinyl acetate hydrolyzed to at least an extent of 60% by weight, preferably 80% by weight.
  • the amount of hardening agent, in particular tetraalkyl orthosilicate, is preferably at least 0.2 parts per part by weight of hydrophilic binder, more preferably between 0.5 and 5 parts by weight, most preferably between 1 parts and 3 parts by weight.
  • the hydrophilic base layer may also contain substances that increase the mechanical strength and the porosity of the layer.
  • colloidal silica may be used.
  • the colloidal silica employed may be in the form of any commercially available water dispersion of colloidal silica for example having an average particle size up to 40 nm, e.g. 20 nm.
  • inert particles of larger size than the colloidal silica may be added e.g. silica prepared according to Stöber as described in J. Colloid and Interface Sci., Vol. 26, 1968, pages 62 to 69 or alumina particles or particles having an average diameter of at least 100 nm which are particles of titanium dioxide or other heavy metal oxides.
  • the surface of the hydrophilic base layer is given a uniform rough texture consisting of microscopic hills and valleys, which serve as storage places for water in background areas.
  • hydrophilic base layers for use in accordance with the present invention are disclosed in EP-A- 601 240 , GB-P- 1 419 512 , FR-P- 2 300 354 , US-P- 3 971 660 , and US-P- 4 284 705 .
  • the amount of silica in the adhesion improving layer is between 200 mg/m 2 and 750 mg/m 2 .
  • the ratio of silica to hydrophilic binder is preferably more than 1 and the surface area of the colloidal silica is preferably at least 300 m 2 /gram, more preferably at least 500 m 2 /gram.
  • the oleophilic layer contains a polymer that is soluble in an aqueous alkaline developer.
  • Preferred polymers are phenolic resins which are soluble in an aqueous developer, preferably having a pH between 7.5 and 14.
  • Suitable polymers are e.g. novolac, resoles, polyvinyl phenols and carboxy-substituted polymers. Typical examples of such polymers are described in DE-A-4007428 , DE-A-4027301 and DE-A-4445820 .
  • the oleophilic layer also contains an organic dye which absorbs visible light so that a perceptible image is obtained upon image-wise exposure and subsequent development.
  • organic dye shall be understood as excluding pigments and metal ion complexes.
  • the dye has an absorption maximum in the visible wavelength region (380-750 nm).
  • the dye may also absorb the infrared light that can be used for the image-wise exposure.
  • the dye does not substantially absorb the light that may be used for the image-wise exposure and then it is advantageous to add an additional sensitizer to the coating that is capable of absorbing the light used for the image-wise exposure. The latter sensitizer is discussed in more detail below.
  • the dye absorbs visible light, it preferably does not sensitize the printing plate precursor, i.e. the coating does not become more soluble in the developer upon exposure to visible light.
  • the coating does not comprise photosensitive ingredients, such as diazide or diazonium compounds, photoacids, photoinitiators, sensitisers etc., which absorb the near UV and/or visible light that is present in sun light or office lighting and thereby render the coating more soluble in exposed areas.
  • the dyes in the materials of the present invention are non-inhibiting, i.e. they do not reduce the solubility of the above polymer in an aqueous alkaline developer.
  • "Reducing the solubility of the polymer” shall be understood as reducing the dissolution rate of the polymer in the developer, rather than reducing the concentration of the dissolved polymer in equilibrium conditions.
  • a positive working material shows a faster dissolution of the oleophilic layer at exposed areas than at unexposed areas.
  • the exposed areas are completely dissolved in the developer before the unexposed areas are attacked so that the latter are characterized by sharp edges and high ink-acceptance. It may be concluded that the solubility differentiation between exposed and unexposed areas of the coating is induced by a kinetic rather than a thermodynamic effect.
  • the inhibiting capability of the dye can easily be tested by coating two samples of the oleophilic layer on a support : the reference sample contains only the polymer and another includes both the polymer (in equal amounts as the reference) as well as the dye.
  • a series of unexposed samples is immersed in an aqueous alkaline developer, each sample during a different time period. After the immersion period, the sample is removed from the developer, immediately rinsed with water, dried and then the dissolution of the coating in the developer is measured by comparing the weight of the sample before and after the development. As soon as the coating is dissolved completely, no more weight loss is measured upon longer immersion time periods, i.e.
  • dissolution time a curve representing weight loss as a function of immersion time reaches a plateau from the moment of complete dissolution of the layer, which is referred to herein as "dissolution time".
  • the non-inhibiting dye is present in an amount sufficient to give the coating a visible color. It is self evident that the required amount depends on the extinction coefficient of the dye.
  • concentration of a typical non-inhibiting dye in the oleophilic layer may vary e.g. between 0.25 and 10.0 wt.% relative to the oleophilic layer, more preferably between 0.5 and 5.0 wt.%.
  • the oleophilic layer may further contain other ingredients, e.g. additional binders to improve the run length of the plate, such as those described in EP-A 933 682 .
  • additional binders to improve the run length of the plate, such as those described in EP-A 933 682 .
  • development accelerators are included, i.e. compounds which act as dissolution promoters because they are capable of reducing the dissolution time of the oleophilic layer, which can be tested by the same procedure as describe above in relation to the inhibiting capability of the dye.
  • cyclic acid anhydrides, phenols or organic acids can be used in order to improve the aqueous developability.
  • cyclic acid anhydride examples include phthalic anhydride, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, 3,6-endoxy- 4-tetrahydrophthalic anhydride, tetrachlorophthalic anhydride, maleic anhydride, chloromaleic anhydride, alpha - phenylmaleic anhydride, succinic anhydride, and pyromellitic anhydride, as described in U.S. Patent No. 4,115,128 .
  • phenols examples include bisphenol A, p-nitrophenol, p-ethoxyphenol, 2,4,4'-trihydroxybenzophenone, 2,3,4-trihydroxy-benzophenone, 4-hydroxybenzophenone, 4,4',4"-trihydroxy-triphenylmethane, and 4,4',3",4"-tetrahydroxy-3,5,3',5'-tetramethyltriphenyl-methane, and the like.
  • organic acids include sulfonic acids, sulfinic acids, alkylsulfuric acids, phosphonic acids, phosphates, and carboxylic acids, as described in, for example, JP-A Nos. 60-88,942 and 2-96,755 .
  • organic acids include p-toluenesulfonic acid, dodecylbenzenesulfonic acid, p-toluenesulfinic acid, ethylsulfuric acid, phenylphosphonic acid, phenylphosphinic acid, phenyl phosphate, diphenyl phosphate, benzoic acid, isophthalic acid, adipic acid, p-toluic acid, 3,4-dimethoxybenzoic acid, phthalic acid, terephthalic acid, 4-cyclohexene-1,2-dicarboxylic acid, erucic acid, lauric acid, n-undecanoic acid, and ascorbic acid.
  • the amount of the cyclic acid anhydride, phenol, or organic acid contained in the image forming composition is preferably in the range of 0.05 to 20% by weight.
  • the coating also contains developer resistance means, i.e. one or more materials which prevent penetration of the aqueous alkaline developer into the oleophilic layer at unexposed areas.
  • developer resistance means can be added to the oleophilic layer or in a barrier layer provided on top of the oleophilic layer.
  • solubility of the barrier layer in the developer or the penetrability of the barrier layer by the developer can be reduced by exposure to heat or infrared light, as described in e.g. EP-A 864 420 , EP-A 950 517 and WO99/21725 .
  • the developer resistance means include water-repellent polymers such as a polymer comprising siloxane and/or perfluoroalkyl units.
  • the barrier layer contains such a water-repellent polymer in an amount between 0.5 and 25 mg/m 2 , preferably between 0.5 and 15 mg/m 2 and most preferably between 0.5 and 10 mg/m 2 .
  • the water-repellent polymer is also ink-repelling, e.g. in the case of polysiloxanes, higher amounts than 25 mg/m 2 can result in poor ink-acceptance of the non-exposed areas.
  • An amount lower than 0.5 mg/m 2 on the other hand may lead to an unsatisfactory development resistance.
  • the polysiloxane may be a linear, cyclic or complex cross-linked polymer or copolymer.
  • the term polysiloxane compound shall include any compound which contains more than one siloxane group -Si(R,R')-O-, wherein R and R' are optionally substituted alkyl or aryl groups.
  • Preferred siloxanes are phenylalkylsiloxanes and dialkylsiloxanes.
  • the number of siloxane groups in the (co)polymer is at least 2, preferably at least 10, more preferably at least 20. It may be less than 100, preferably less than 60.
  • the water-repellant polymer is a block-copolymer or a graft-copolymer of a poly(alkylene oxide) and a polymer comprising siloxane and/or perfluoroalkyl units.
  • a suitable copolymer comprises about 15 to 25 siloxane units and 50 to 70 alkyleneoxide groups.
  • Preferred examples include copolymers comprising phenylmethylsiloxane and/or dimethylsiloxane as well as ethylene oxide and/or propylene oxide, such as Tego Glide 410, Tego Wet 265, Tego Protect 5001 or Silikophen P50/X, all commercially available from Tego Chemie, Essen, Germany.
  • Such a copolymer acts as a surfactant which upon coating, due to its bifunctional structure, automatically positions itself at the interface between the coating and air and thereby forms a separate top layer even when applied as an ingredient of the coating solution of the oleophilic layer. Simultaneously, such surfactants act as a spreading agent which improves the coating quality.
  • the water-repellent polymer can be applied in a second solution, coated on top of the oleophilic layer. In that embodiment, it may be advantageous to use a solvent in the second coating solution that is not capable of dissolving the ingredients present in the first layer so that a highly concentrated water-repellent phase is obtained at the top of the material.
  • the material can be image-wise exposed directly with heat, e.g. by means of a thermal head, or indirectly by infrared light, which is converted into heat by a light absorbing compound. Near infrared light is preferred.
  • the coating comprises, in addition to the non-inhibiting dye, a sensitizer which is a dye or pigment having an absorption maximum in the IR wavelength range.
  • concentration of the sensitizing dye or pigment in the oleophilic layer is typically between 0.25 and 10.0 wt.%, more preferably between 0.5 and 7.5 wt.% relative to said layer.
  • Preferred IR-absorbing compounds are dyes such as cyanine or merocyanine dyes or pigments such as carbon black.
  • a suitable compound is the following infrared dye :
  • the sensitizing dye or pigment may be present in the oleophilic layer, in the barrier layer discussed above or in an optional other layer.
  • the dye or pigment is concentrated in or near the barrier layer, e.g. in an intermediate layer between the oleophilic and the barrier layer.
  • said intermediate layer comprises the light absorbing compound in an amount higher than the amount of light absorbing compound in the oleophilic or in the barrier layer.
  • the barrier layer consists essentially of water-repellent polymer, i.e. comprises no effective amount of sensitizer or other ingredients.
  • the printing plate precursor of the present invention can be exposed to heat or to infrared light, e.g. by means of a thermal head, LEDs or a laser.
  • the light used for the exposure is a laser emitting near infrared light having a wavelength in the range from about 750 to about 1500 nm is used, such as a semiconductor laser diode, a Nd:YAG or a Nd:YLF laser.
  • the required laser power depends on the sensitivity of the image-recording layer, the pixel dwell time of the laser beam, which is determined by the spot diameter (typical value of modern plate-setters at 1/e 2 of maximum intensity : 10-25 ⁇ m), the scan speed and the resolution of the exposure apparatus (i.e. the number of addressable pixels per unit of linear distance, often expressed in dots per inch or dpi; typical value : 1000-4000 dpi).
  • ITD plate-setters for thermal plates are typically characterized by a very high scan speed up to 500 m/sec and may require a laser power of several Watts.
  • the known plate-setters can be used as an off-press exposure apparatus, which offers the benefit of reduced press down-time.
  • XTD plate-setter configurations can also be used for on-press exposure, offering the benefit of immediate registration in a multi-color press. More technical details of on-press exposure apparatuses are described in e.g. US 5,174,205 and US 5,163,368 .
  • the non-image areas of the coating are removed by immersion in an aqueous alkaline developer, which may be combined with mechanical rubbing, e.g. by a rotating brush.
  • the development step may be followed by a rinsing step, a gumming step, a drying step and/or a post-baking step.
  • the printing plate thus obtained can be used for conventional, so-called wet offset printing, in which ink and an aqueous dampening liquid is supplied to the plate.
  • Another suitable printing method uses so-called single-fluid ink without a dampening liquid.
  • Single-fluid inks which are suitable for use in the method of the present invention have been described in US 4,045,232 ; US 4,981,517 and US 6,140,392 .
  • the single-fluid ink comprises an ink phase, also called the hydrophobic or oleophilic phase, and a polyol phase as described in WO 00/32705 .
  • a 0.30 mm thick aluminum foil was degreased by immersing the foil in an aqueous solution containing 5 g/l of sodium hydroxide at 50°C and rinsed with demineralized water.
  • the foil was then electrochemically grained using an alternating current in an aqueous solution containing 4 g/l of hydrochloric acid, 4 g/l of hydroboric acid and 5 g/l of aluminum ions at a temperature of 35°C and a current density of 1200 A/m 2 to form a surface topography with an average center-line roughness Ra of 0.5 ⁇ m.
  • the aluminum foil was then etched with an aqueous solution containing 300 g/l of sulfuric acid at 60°C for 180 seconds and rinsed with demineralized water at 25°C for 30 seconds.
  • the foil was subsequently subjected to anodic oxidation in an aqueous solution containing 200 g/l of sulfuric acid at a temperature of 45°C, a voltage of about 10 V and a current density of 150 A/m 2 for about 300 seconds to form an anodic oxidation film of 3.00 g/m 2 of Al 2 O 3 then washed with demineralized water, post-treated with a solution containing polyvinylphosphonic acid and subsequently with a solution containing aluminum trichloride, rinsed with demineralized water at 20°C during 120 seconds and dried.
  • Novolac Alnovol SPN452 from Clariant, a 40.5 wt.% solution in methoxypropanol
  • Table 1 A layer of novolac (Alnovol SPN452 from Clariant, a 40.5 wt.% solution in methoxypropanol) and the dyes specified in Table 1 were coated on the above support. After drying during 2 min at 120°C, the samples contained 0.9 g/m 2 of novolac. The samples were then dipped in an Ozasol EP26 developer from Agfa at 20°C and the dissolution time was determined as described above. Examples 2-4 contained a dye according to the invention and showed shorter dissolution time values than Reference Example 1 without dye. Comparative Example 5 contained Resolin Rot F3BS, which is an inhibiting dye, inducing a longer dissolution time than for the materials of the present invention. Table 1 Example no.
  • the solutions in Table 2 were coated on the above support at a wet coating thickness of 22 ⁇ m and then dried during 2 min at 120°C.
  • the materials were then imaged on a Creo Trendsetter 3244 (830 nm) using the following series of energy density settings (power at the image plane) : 79 mJ/cm 2 , 99 mJ/cm 2 , 125 mJ/cm 2 , 157 mJ/cm 2 , and 197 mJ/cm 2 .
  • the plates were then processed in an Agfa Autolith PN85 processor operating at a speed of 0.84 m/min using Agfa Ozasol EP26 developer at 25°C and finally gummed with Agfa Ozasol RC795.
  • the IR-sensitivity was defined as the energy density that is required to obtain a 50% light absorption, measured on the developed plate at the wavelength maximum of the dye, in areas which have been exposed with a dot area of a 50% screen (@200 lpi).

Landscapes

  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials For Photolithography (AREA)
  • Printing Plates And Materials Therefor (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)

Claims (8)

  1. Eine wärmeempfindliche lithografische Druckplattenvorstufe mit (i) einem Träger, der eine hydrophile Oberfläche aufweist oder mit einer hydrophilen Schicht versehen ist, und (ii) einer darüber aufgetragenen Beschichtung, wobei die Beschichtung eine oleophile Schicht aufweist, die bei bildmäßiger Erwärmung oder bildmäßiger Belichtung mit Infrarotlicht und anschließender Eintauchung in einen wässrig-alkalischen Entwickler im Entwickler gelöst wird und zwar bei einer höheren Lösungsgeschwindigkeit in den belichteten Bereichen als in den nicht-belichteten Bereichen, wobei die oleophile Schicht :
    (a) ein im Entwickler lösliches Polymer,
    (b) eine Infrarotlicht absorbierende Verbindung,
    (c) und einen organischen Farbstoff in einer Menge, die hinreicht, um der Beschichtung eine sichtbare Farbe zu verleihen, enthält,
    dadurch gekennzeichnet, dass der organische Farbstoff die Lösungsgeschwindigkeit der nicht-belichteten Bereiche im Entwickler nicht verringert und eine chemische Struktur gemäß einer der folgenden Formeln aufweist :
    Figure imgb0014
    Figure imgb0015
    Figure imgb0016
    Figure imgb0017
     in denen :
    - i und j unabhängig voneinander 0 bis 3 bedeuten,
    - k, l und o unabhängig voneinander 0 bis 4 bedeuten,
    - m und n unabhängig voneinander 0 bis 5 bedeuten,
    - p 0 bis 3 bedeutet,
    - R1, R1', R1 " , R2 und R2' unabhängig voneinander jeweils eine gegebenenfalls substituierte Alkylgruppe, eine gegebenenfalls substituierte Arylgruppe, -G, -L-G , -CN, ein Halogenatom,
    - NO2, -ORd, -CO-O-Ra, -O-CO-Ra, -CO-NRdRe, -NRdRe, -NRd-CO-Ra,
    - NRd-CO-O-Ra, -NRd-CO-NReRf, -SO2-O-Ra oder -SO2-NRdRe bedeuten oder zwei benachbarte Radikale R1, R1 ' , R1 " , R2 oder R2 ' zusammen einen anellierten carbocyclischen oder heterocyclischen Ring bilden, und
    - R3, R4 und R5 unabhängig voneinander jeweils ein Wasserstoffatom, eine gegebenenfalls substituierte Alkylgruppe, eine gegebenenfalls substituierte Arylgruppe, -CO-Rb, -CO-O-Rb, -CO-NRfRg oder -L-G bedeuten,
    wobei
    - Ra und Rb eine gegebenenfalls substituierte Alkylgruppe oder eine gegebenenfalls substituierte Arylgruppe bedeuten,
    - Rd, Re, Rf und Rg ein Wasserstoffatom, eine gegebenenfalls substituierte Alkylgruppe oder eine gegebenenfalls substituierte Arylgruppe bedeuten,
    - G eine anionische Gruppe ist oder eine Gruppe, die durch Eintauchen der Beschichtung in den Entwickler anionisch gemacht werden kann, und
    - L eine zweiwertige Verbindungsgruppe bedeutet,
    vorausgesetzt, der organische Farbstoff enthält zumindest eine Gruppe G.
  2. Lithografische Druckplattenvorstufe nach Anspruch 1, dadurch gekennzeichnet, dass G unabhängig -COOH, -OH, -PO3H2, -O-PO3H2, -SO3H, -O-SO3H, -SO2-NH2, -SO2-NH-R, -SO2-NH-CO-R oder ein daraus gebildetes Salz ist, wobei R eine gegebenenfalls substituierte Alkylgruppe oder eine gegebenenfalls substituierte Arylgruppe bedeutet.
  3. Lithografische Druckplattenvorstufe nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass die oleophile Schicht ferner eine die Lösungsgeschwindigkeit der nicht-belichteten Bereiche im Entwickler steigernde Verbindung enthält.
  4. Lithografische Druckplattenvorstufe nach Anspruch 3, dadurch gekennzeichnet, dass die die Lösungsgeschwindigkeit der nicht-belichteten Bereiche steigernde Verbindung ein cyclisches Säureanhydrid, ein Phenol oder eine organische Säure ist.
  5. Lithografische Druckplattenvorstufe nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass die Beschichtung ferner Mittel enthält, die die Beständigkeit der Beschichtung gegen den Entwickler steigern, wobei die Beständigkeit der Beschichtung gegen den Entwickler bei Erwärmung oder Belichtung mit Infrarotlicht verringert wird.
  6. Lithografische Druckplattenvorstufe nach Anspruch 5, dadurch gekennzeichnet, dass die Mittel zum Steigern der Beständigkeit der Beschichtung gegen den Entwickler in einer auf die oleophile Schicht aufgetragenen Sperrschicht enthalten sind und die Löslichkeit der Sperrschicht im Entwickler oder die Durchdringbarkeit des Entwicklers in die Sperrschicht bei Erwärmung oder Belichtung mit Infrarotlicht verringert wird.
  7. Lithografische Druckplattenvorstufe nach Anspruch 5 oder 6, dadurch gekennzeichnet, dass die Mittel zum Steigern der Beständigkeit der Beschichtung gegen den Entwickler ein wasserabstoßendes Polymer enthalten.
  8. Lithografische Druckplattenvorstufe nach Anspruch 7, dadurch gekennzeichnet, dass das wasserabstoßende Polymer
    - ein Polymer mit Siloxan- und/oder Perfluoralkyleinheiten oder
    - ein Blockcopolymer oder Pfropfcopolymer eines Poly(alkylenoxids) und eines Polymers mit Siloxan- und/oder Perfluoralkyleinheiten ist.
EP02102309A 2001-09-24 2002-09-05 Wärmeempfindlicher positiv arbeitender Flachdruckplattenvorläufer Expired - Fee Related EP1295717B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP02102309A EP1295717B1 (de) 2001-09-24 2002-09-05 Wärmeempfindlicher positiv arbeitender Flachdruckplattenvorläufer

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP01000495 2001-09-24
EP01000495 2001-09-24
EP02102309A EP1295717B1 (de) 2001-09-24 2002-09-05 Wärmeempfindlicher positiv arbeitender Flachdruckplattenvorläufer

Publications (3)

Publication Number Publication Date
EP1295717A2 EP1295717A2 (de) 2003-03-26
EP1295717A3 EP1295717A3 (de) 2003-07-16
EP1295717B1 true EP1295717B1 (de) 2007-07-25

Family

ID=26076418

Family Applications (1)

Application Number Title Priority Date Filing Date
EP02102309A Expired - Fee Related EP1295717B1 (de) 2001-09-24 2002-09-05 Wärmeempfindlicher positiv arbeitender Flachdruckplattenvorläufer

Country Status (1)

Country Link
EP (1) EP1295717B1 (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1588847B1 (de) * 2004-04-21 2007-05-09 Agfa Graphics N.V. Verfahren zur genauen Belichtung von kleinen Punkten auf eine Wärmeempfindliche positiv arbeitende Flachdruckplatte
US7467587B2 (en) 2004-04-21 2008-12-23 Agfa Graphics, N.V. Method for accurate exposure of small dots on a heat-sensitive positive-working lithographic printing plate material

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1084070A (en) 1960-08-05 1967-09-20 Kalle Ag Process and material for the preparation of planographic printing plates
DE4417907A1 (de) 1994-05-21 1995-11-23 Hoechst Ag Verfahren zur Nachbehandlung von platten-, folien- oder bandförmigem Material, Träger aus derartigem Material und seine Verwendung für Offsetdruckplatten
DE4423140A1 (de) 1994-07-01 1996-01-04 Hoechst Ag Hydrophiliertes Trägermaterial und damit hergestelltes Aufzeichnungsmaterial
EP0825927B1 (de) * 1996-04-23 1999-08-11 Kodak Polychrome Graphics Company Ltd. Vorläufer einer lithographischen druckform und ihre verwendung bei der bebilderung durch wärme
JP3814961B2 (ja) 1996-08-06 2006-08-30 三菱化学株式会社 ポジ型感光性印刷版
GB9617415D0 (en) * 1996-08-20 1996-10-02 Minnesota Mining & Mfg Production of colour proofs and printing plates
EP0855267B1 (de) * 1997-01-24 2002-04-17 Fuji Photo Film Co., Ltd. Flachdruckplatte
EP0864420B2 (de) 1997-03-11 2005-11-16 Agfa-Gevaert Wärmempfindliches Aufzeichnungselement zur Herstellung von positiv arbeitenden Flachdruckformen
DE69810242T2 (de) * 1997-10-28 2003-10-30 Mitsubishi Chem Corp Positiv arbeitendes strahlungsempfindliches Gemisch, positiv arbeitende lichtempfindliche Flachdruckplatte und Verfahren zur Bebilderung der Druckplatte
GB9722862D0 (en) 1997-10-29 1997-12-24 Horsell Graphic Ind Ltd Pattern formation
EP0938972B1 (de) * 1998-02-27 2002-11-13 Fuji Photo Film Co., Ltd. Photoempfindliche Druckplatte mit einem Bildaufzeichnungsmaterial
EP0950517B1 (de) 1998-04-15 2001-10-04 Agfa-Gevaert N.V. Wärmeempfindliches Aufzeichnungsmaterial zur Herstellung von positiv arbeitenden Druckplatten

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Also Published As

Publication number Publication date
EP1295717A3 (de) 2003-07-16
EP1295717A2 (de) 2003-03-26

Similar Documents

Publication Publication Date Title
EP1506854B1 (de) Verfahren zum Nacheinbrennen von lithographischen Druckplatten
EP1554347B1 (de) Polymer für wärmeemfindlicher lithographischer druckplattevorläufer
EP1594696B1 (de) Wärmeempfindlicher lithographischer druckplattenvorläufer
US6641976B2 (en) Method of making a negative-working heat-sensitive lithographic printing plate precursor
EP1554346B1 (de) Polymer für wärmeempfindliche lithographische druckplattenvorläufer
EP1554324B1 (de) Polymer für wärmeempfindlichen vorläufer einer lithographischen druckplatte
EP1738901B1 (de) Wärmeempfindlicher lithographischer Druckplattenvorläufer
EP1554117A1 (de) Wärmeempfindlicher vorläufer für eine lithographische druckplatte
EP1506858A2 (de) Wärmeempfindlicher lithographischer Druckplattevorläufer
US20050037280A1 (en) Heat-sensitive lithographic printing plate precursor
US7041427B2 (en) Heat-sensitive lithographic printing plate precursor
US20070003870A1 (en) Heat-sensitive lithographic printing plate precursor
EP1738900B1 (de) Wärmeempfindlicher Flachdruckplattenvorläufer
EP1243413B1 (de) Verfahren zur Herstellung einer negativarbeitenden, wärmeempfindlichen, lithographischen Druckplattenvorstufe
US20050037287A1 (en) Method for postbaking a lithographic printing plate
EP1297950B1 (de) Wärmeempfindlicher lithographischer Druckplattenvorläufer
US20040048195A1 (en) Heat-sensitive lithographic printing plate precursor
US6846613B2 (en) Positive-working lithographic printing plate precursors
EP1256444B1 (de) Positivarbeitende lithographische Druckplattenvorläufer
US7294447B2 (en) Positive-working lithographic printing plate precursor
EP1295717B1 (de) Wärmeempfindlicher positiv arbeitender Flachdruckplattenvorläufer
EP1249341A1 (de) Flachdruckplattenvorläufer
EP1396338B1 (de) Wärmeempfindlicher Flachdruckplattenvorläufer
US20070003869A1 (en) Heat-sensitive lithographic printing plate-precursor
EP1243410A1 (de) Verfahren zur Herstellung eines wärmeempfindlichen Vorläufers für eine Flachdruckplatte

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LI LU MC NL PT SE SK TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LI LU MC NL PT SE SK TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

17P Request for examination filed

Effective date: 20040116

AKX Designation fees paid

Designated state(s): DE FR GB NL

17Q First examination report despatched

Effective date: 20040326

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: AGFA GRAPHICS

RIN1 Information on inventor provided before grant (corrected)

Inventor name: VERMEERSCH, JOANAGFA-GEVAERT

Inventor name: VAN DAMME, MARC,AGFA-GEVAERT

Inventor name: DEROOVER, GEERT,AGFA-GEVAERT

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB NL

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 60221329

Country of ref document: DE

Date of ref document: 20070906

Kind code of ref document: P

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20080428

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 15

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 16

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 60221329

Country of ref document: DE

Owner name: AGFA NV, BE

Free format text: FORMER OWNER: AGFA GRAPHICS N.V., MORTSEL, BE

REG Reference to a national code

Ref country code: NL

Ref legal event code: HC

Owner name: AGFA NV; BE

Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), CHANGE OF OWNER(S) NAME; FORMER OWNER NAME: AGFA GRAPHICS N.V.

Effective date: 20180126

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 17

REG Reference to a national code

Ref country code: FR

Ref legal event code: CD

Owner name: AGFA NV, BE

Effective date: 20180628

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20190730

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20190731

Year of fee payment: 18

Ref country code: DE

Payment date: 20190731

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20190731

Year of fee payment: 18

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 60221329

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MM

Effective date: 20201001

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20200905

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201001

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210401

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200930

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200905