FIELD OF THE INVENTION
[0001] The present invention relates to a heat-sensitive imaging element for making lithographic
printing plates. More specifically the invention relates to a heat-sensitive imaging
element which requires no processing.
BACKGROUND OF THE INVENTION
[0002] Lithographic printing is the process of printing from specially prepared surfaces,
some areas of which are capable of accepting ink, whereas other areas will not accept
ink.
[0003] In the art of photolithography, a photographic material is made imagewise receptive
to oily or greasy ink in the photo-exposed (negative working) or in the non-exposed
areas (positive working) on a ink-repelling background.
[0004] In the production of common lithographic plates, also called surface litho plates
or planographic printing plates, a support that has affinity to water or obtains such
affinity by chemical treatment is coated with a thin layer of a photosensitive composition.
Coatings for that purpose include light-sensitive polymer layers containing diazo
compounds, dichromate-sensitized hydrophilic colloids and a large variety of synthetic
photopolymers. Particularly diazo-sensitized systems are widely used.
[0005] Upon imagewise exposure of such light-sensitive layer the exposed image areas become
insoluble and the unexposed areas remain soluble. The plate is then developed with
a suitable liquid to remove the diazonium salt or diazo resin in the unexposed areas.
[0006] On the other hand, methods are known for making printing plates involving the use
of imaging elements that are heat-sensitive rather than photosensitive. A particular
disadvantage of photosensitive imaging elements such as described above for making
a printing plate is that they have to be shielded from the light. Furthermore they
have a problem of stability of sensitivity in view of the storage time and they show
a lower resolution. The trend towards heat-sensitive printing plate precursors is
clearly seen on the market.
[0007] EP-A- 444 786, JP- 63-208036,and
JP- 63-274592 disclose photopolymer resists that are sensitized to the near IR. So far, none has
proved commercially viable and all require wet development to wash off the unexposed
regions.
EP-A- 514 145 describes a laser addressed plate in which heat generated by the laser exposure causes
particles in the plate coating to melt and coalescence and hence change their solubility
characteristics. Once again, wet development is required.
EP-A- 652 483 discloses a lithographic printing plate requiring no dissolution processing which
comprises a substrate bearing a heat-sensitive coating, which coating becomes relatively
more hydrophilic under the action of heat. Said system yields a positive working printing
plate.
EP-A- 609 941 describes a heat-mode recording material comprising on a substrate a metallic layer
and a thin hydrophobic layer which becomes hydrophilic upon exposure. However the
lithographic performance of the obtained printing plate is poor.
OBJECTS OF THE INVENTION
[0008] It is an object of the present invention to provide a heat-sensitive imaging element
for preparing lithographic printing plates requiring no dissolution processing and
having a high lithographic performance (ink acceptance, scratch resistance , durability)
SUMMARY OF THE INVENTION
[0009] According to the present invention there is provided a heat-sensitive imaging element
for making lithographc printing plates comprising on a lithographic base, having a
hydrophilic surface, a metallic layer or metal oxide layer and on top thereof an oleophobic
polymeric layer having a thickness of less than 5µm characterised in that said polymeric
layer comprises a polymer containing phenolic groups.
DETAILED DESCRIPTION OF THE INVENTION
[0010] It has been found that according to the present invention, using an imaging element
as described above, lithographic printing plates requiring no processing and having
an excellent lithographic performance can be obtained.
[0011] Metallic layers or metal oxide layers suitable for use in accordance with the invention
comprise metals or metal oxides converting the actinic radiation to heat so that the
oleophobicity of the oleophobic top-layer is destroyed. The thickness of the metallic
layer or metal oxide layer is preferably from 0.01µm to 2µm, and most preferably from
0.05µm to 1.5 µm. Specific examples of metal layers or metal oxide layers are aluminum,
titanium oxide, bismuth and silver of which the three latter are preferred.
[0012] A silver layer for use in this invention as the metallic layer can be made according
to the principles of the silver complex diffusion transfer reversal process, hereinafter
called DTR-process, having been described e.g. in US-P 2,352,014 and in the book "Photographic
Silver Halide Diffusion Processes" by André Rott and Edith Weyde - The Focal Press
- London and New York, (1972).
[0013] In the DTR-process non-developed silver halide of an information-wise exposed photographic
silver halide emulsion layer material is transformed with a so-called silver halide
solvent into soluble silver complex compounds which are allowed to diffuse into an
image-receiving element and are reduced therein with a developing agent, generally
in the presence of physical development nuclei, to form a silver image having reversed
image density values ('DTR-image') with respect to the black silver image obtained
in the exposed areas of the photographic material.
[0014] In another method for providing a metal layer on the lithographic base having a hydrophilic
surface a silver halide emulsion disposed on a lithographic base having a hydrophilic
surface is strongly exposed to actinic radiation and then developed, or otherwise
processed to maximum blackness. The black opaque emulsion is converted to a reflective
recording material by heating at least to 270 °C in an oxygen containing environment
until the emulsion coating assumes a shiny reflective appearance. Such method is disclosed
in
US-P-4 314 260.
[0015] According to an alternative method for providing a metal layer on the lithographic
base the metal is provided using vapour or vacuum deposition.
[0016] According to another embodiment of the invention the metallic layer can be a bismuth
layer that can be provided by vacuum deposition.
[0017] A drawback of the method of preparation of a thin bismuth recording layer by vacuum
deposition is the fact that this is a complicated, cumbersome and expensive process.
[0018] Therefore, in
EP-A- 97201282 the vacuum deposition is replaced by coating from an aqueous medium. According to
this disclosure a thin metal layer is formed by the following steps :
(1) preparing an aqueous medium containing ions of a metal,
(2) reducing said metal ions by a reducing agent thus forming metal particles,
(3) coating said aqueous medium containing said metal particles on a transparent support.
[0019] As a metal oxide layer preferably a titanium oxide layer is used. This layer can
be applied to the substrate by vacuum deposition, electron-beam evaporation or sputtering.
[0020] The oleophobic layer provided on top of the metallic layer or metal oxide layer comprises
a polymer containing phenolic groups. Preferred polymers containing phenolic groups
are phenolic resins (e.g. novolac) or hydroxyphenyl substituted polymers (e.g. polyhydroxystyrenes).
The oleophobic layer has a thickness of less than 5µm. As a consequence a highly sensitive
heat-sensitive imaging element is obtained. The use of a polymer containing phenolic
groups furthermore improves the lithographic performance ( ink acceptance, scratch
resistance, durability) of the lithographic printing plates obtained according to
the present invention.
[0021] According to one embodiment of the present invention, the lithographic base having
a hydrophilic surface can be an anodised aluminum. A particularly preferred lithographic
base having a hydrophilic surface is an electrochemically grained and anodised aluminum
support. Most preferably said aluminum support is grained in nitric acid, yielding
imaging elements with a higher sensitivity. According to the present invention, an
anodised aluminum support may be treated to improve the hydrophilic properties of
its surface. For example, the aluminum support may be silicated by treating its surface
with a sodium silicate solution at elevated temperature, e.g. 95°C. Alternatively,
a phosphate treatment may be applied which involves treating the aluminum oxide surface
with a phosphate solution that may further contain an inorganic fluoride. Further,
the aluminum oxide surface may be rinsed with a citric acid or citrate solution. This
treatment may be carried out at room temperature or can 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. Still further, the
aluminum oxide surface may be treated with polyvinylphosphonic acid, polyvinylmethylphosphonic
acid, phosphoric acid esters of polyvinyl alcohol, polyvinylsulphonic acid, polyvinylbenzenesulphonic
acid, sulphuric acid esters of polyvinyl alcohol, and acetals of polyvinyl alcohols
formed by reaction with a sulphonated aliphatic aldehyde. It is further evident that
one or more of these post treatments may be carried out alone or in combination.
[0022] According to another embodiment in connection with the present invention, the lithographic
base can comprise a flexible support, such as e.g. paper or plastic film, provided
with a hardened hydrophilic layer. A particularly suitable hardedned rough hydrophilic
layer may be obtained from a hydrophilic binder hardened with a hardening agent such
as formaldehyde, glyoxal, polyisocyanate or preferably a hydrolysed tetra-alkylorthosilicate.
[0023] As hydrophilic binder there may be used hydrophilic (co)polymers such as for example,
homopolymers and copolymers of vinyl alcohol, acrylamide, methylol acrylamide, methylol
methacrylamide, acrylic acid, methacrylic acid, hydroxyethyl acrylate, hydroxyethyl
methacrylate or maleic anhydride/vinylmethylether copolymers.
[0024] A hardened hydrophilic layer on a flexible support used in accordance with the present
embodiment preferably also contains substances that increase the mechanical strength
and the porosity of the layer e.g. colloidal silica. In addition inert particles of
larger size than the colloidal silica can 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. Incorporation
of these particles gives the surface of the hardened hydrophilic layer a uniform rough
texture consisting of microscopic hills and valleys.
[0025] The thickness of the hardened hydrophilic layer may vary in the range of 0.2 to 25
µm and is preferably 1 to 10 µm.
[0026] Particular examples of suitable hardened hydrophilic layers for use in accordance
with the present invention are disclosed in
EP-A 601 240, GB-P-1 419 512, FR-P-230 354, US-P-3 971 660, US-P-4 284 705 and
EP-A 514 490.
[0027] As support on which the hydrophilic layer is provided it is particularly preferred
to use a plastic film e.g. substrated polyethylene terephthalate film, cellulose acetate
film, polystyrene film, polycarbonate film etc... The plastic film support may be
opaque or transparent.
[0028] It is particularly preferred to use a polyester film support to which an adhesion
improving layer has been provided. Particularly suitable adhesion improving layers
for use in accordance with the present invention comprise a hydrophilic binder and
colloidal silica as disclosed in
EP-A- 619 524, EP-A- 620 502 and EP-A- 619 525. Preferably, the amount of silica in the adhesion improving layer is between 200
mg per m
2 and 750 mg per m
2. Further, 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 per gram, more preferably a surface area of 500 m
2 per gram.
[0029] In accordance to the method of the present invention for obtaining a lithographic
printing plate the heat-sensitive imaging element is image-wise scanning exposed using
a laser, preferably a laser that operates in the infrared or near-infrared, i.e. wavelenght
range of 700-1500nm. Most preferred are laser diodes emitting in the near-infrared.
[0030] After the exposure the imaging element can be used without an additional wet treatment
as a lithographic printing plate.
[0031] The printing plate obtained according to the present invention can also be used in
the printing process as a seamless sleeve printing plate. This cylindrical printing
plate wich has as diameter the diameter of the print cylinder is slided on the print
cylinder instead of applying in a classical way a classically formed printing plate.
More details on sleeves are given in 'Grafisch Nieuws' ed. Keesing, 15, 1995, page
4 to 6.
[0032] The following examples illustrate the present invention without limiting it thereto.
All parts and percentages are by weight unless otherwise specified.
EXAMPLES
Example 1
Preparation of the DTR material
[0033] On the back of a polyethylene terephtalate support with a thickness of 175 µ, was
coated a layer from a 11% wt solution in demineralized water ( pH=4), with a wet thickness
of 50 µm. The resulting layer contained 74.7% of titaniumdioxide, 8.6% of polyvinylalcohol,
16.2% of hydrolysed tetramethylorthosilicate and 0.5% wetting agents.
[0034] On the other side of the polyethylene terephtalate support which is provided with
a hydrophilic subbing layer, is first coated a layer from a 20% wt solution in demineralized
water ( pH=4), with a wet coating thickness of 50 µm. This layer contained 82.7% of
titaniumdioxide, 9.1% of polyvinylalcohol, 8.2% of hydrolysed tetramethylorthosilicate
and 0.17‰ of palladiumsulphide (particle size 2-3 nm). On this base layer, a layer
of palladiumsulphide particles (2-3 nm) is coated from a 0.24‰ wt solution (pH=9)
in demineralized water, with a wet thickness of 13 µm. Finally, an emulsion layer
and top layer were simultaneously coated by means of the cascade coating technique.
The emulsion layer was coated with a wet thickness of 30 µm and such that the silver
halide coverage expressed as AgNO
3 was 2.50 g/m
2 and the gelatin content was 1.50 g/m
2. The toplayer was coated with a wet thickness of 15 µm such that the gelatin content
was 0.7 g/m
2. The top layer further contained 61 mg/m
2 of Levanyl Rot and 0.14 g/m
2 matting agent.
Preparation of the heat-sensitive imaging element
[0035] To obtain a heat-sensitive imaging element according to the present invention, the
unexposed DTR material as described above was developed for 12s at 24 °C in an aqueous
alkaline solution having the following ingredients:
Anhydrous sodium sulphite |
120 g |
Sodium hydroxide |
22 g |
Carboxymethylcellulose |
4 g |
Potassium bromide |
0.75 g |
Anhydrous sodium thiosulphate |
8 g |
Aluminum sulphate.18H2O |
8 g |
Ethylene diamine tetraacetic acid tetrasodium salt |
4.2 g |
Hydroquinone |
20 g |
Methylfenidon |
6.25 g |
Demineralized water to make |
1L |
pH (25°C) > 12.5 |
|
[0036] The initiated diffusion transfer was allowed to continue for 18 s to form a silver
layer, whereafter the material was rinsed with water containing 0.03‰ of trypsine
at 50 °C.
[0037] The thus obtained metallic silver layer was provided with a hydrophobic layer by
guiding the material through a finisher at 45°C, having the following composition:
Dextran 70000 |
40 g |
Polyethyleneglycol 200 |
50 ml |
Sodiumdihydrogenphosphate.2H2O |
20 g |
Citric acid |
22 g |
Potassium nitrate |
12.5 g |
Sodium hydroxide |
12.6 g |
1-phenyl-5-mercaptotetrazole |
0.5 g |
Biocide |
0.1 g |
Wetting agent |
261.5 mg |
Demineralized water to make |
1L |
pH (25°C) = 5.95 |
|
Exposing the heat-sensitive imaging element
[0038] This material was imaged with:
1. a Gerber C42T™ internal drum platesetter at 275 m/s and 2540 dpi. The power level
of the laser in the image plane was 5.4 W.
2. an Isomet diode external drum platesetter at 3.2 m/s and 5 3600 dpi. The power
level in the image plane was 253 mW.
Printing the imagewise exposed element
[0039] 0 The plates were both printed on a Heidelberg GTO46 printing machine with a conventional
ink (Van Son rubberbase) and fountain solution (Rotamatic), resulting in excellent
prints without any scumming in the IR-exposed areas and good ink-uptake in the unexposed
areas. The printing results with respect to image quality 5 are presented in tabel
1.
Tabel1
Laser |
Dot rendering |
Dot rendering |
|
(100th print - 200 lpi) |
40% |
50% |
70% screen |
Internal drum |
4 - 91 |
61 |
73 |
91 |
External drum |
2 - 94 |
64 |
75 |
88 |
Example 2
Preparation of the DTR material
[0040] The DTR material was prepared as described in example 1.
Preparation of the heat-sensitive imaging element
[0041] To obtain a heat-sensitive imaging element according to the present invention, the
unexposed DTR material was developed for 12s at 24 °C in an aqueous alkaline solution
as described in example 1.
[0042] The initiated diffusion transfer was allowed to continue for 18 s to form a silver
layer, whereafter the material was rinsed with water at 50 °C.
[0043] One of the thus obtained metallic silver layers was used as such, one was coated
with a polyethylene layer (2 g/m
2) and a 3th one was coated with a novolac layer (2 g/m
2 Alnovol SPN452).
[0044] A 4th material was prepared as described in example 1.
Exposing the heat-sensitive imaging element
[0045] The 4 materials were all imaged with a Gerber C42T™ internal drum platesetter at
12,000 rpm (367 m/s, pixel dwell time 0.032 µs) and 2540 dpi. The power level of the
laser in the image plane was 5.4 W.
[0046] After imaging, the plates were printed without any additional wet treatment.
Printing the imagewise exposed element
[0047] The plates were printed on a Heidelberg GTO46 printing machine under more critical
conditions than in example 1 with a conventional ink (K+E) and a fountain solution
of 5% G671c (commercialy available from Agfa-Gevaert N.V.) + 10% isopropanol.
[0048] The plate that did not get an extra coating layer after developing, did not show
any ink-uptake in the unexposed areas and the material prepared as described in example
1 showed a slower ink-uptake while the one with polyethylene as a final coating, resulted
in a better ink-uptake and no scumming, but the image was already damaged after 25
prints. Finally the one with the novolac coating on top, showed a good ink-uptake,
no scumming and a runlength > 3000 prints.
Example 3
Preparation of the DTR material
[0049] The DTR material was prepared as described in example 1 or 2.
Preparation of the heat-sensitive imaging element
[0050] To obtain a heat-sensitive imaging element according to the present invention, the
unexposed DTR material was developed for 12s at 24 °C in an aqueous alkaline solution
as described in example 1 or 2.
[0051] The initiated diffusion tranfer was allowed to continue for 18 s to form a silver
layer, whereafter the material was rinsed with water at 50 °C.
[0052] One of the thus obtained metallic silver layers was used as such, one was coated
with a polyethylene layer (1 g/m
2), a third one was coated with a novolac layer (1 g/m
2 Alnovol SPN452) and the last one was coated with a top layer of a copolymer of polyvinylbutyral,
polyvinylalcohol and polyvinylacetate, esterified with trimellitic acid anhydride
(1 g/m
2).
Exposing the heat-sensitive imaging element
[0053] The 4 materials were all imaged with a Gerber C42T™ internal drum platesetter at
12,000 rpm (367 m/s, pixel dwell time 0.032 µs) and 2540 dpi. The power level of the
laser in the image plane was 5.4 W.
[0054] After imaging, the plates were printed without any additional wet treatment.
Printing the imagewise exposed element
[0055] The plates were printed on a Heidelberg GTO46 printing machine with a conventional
ink (K+E) and a fountain solution of 5% G671c (commercially available from Agfa-Gevaert
N.V.) + 10% isopropanol.
[0056] The plate that did not get an extra coating layer after developing, did not show
any ink-uptake in the unexposed areas. The ones with polyethylene and the one with
the copolymer as a final coating, resulted in a good ink-uptake and no scumming, but
the image was already damaged after 25-50 prints. Finally the one with the novolac
coating on top, showed a good ink-uptake, no scumming and a runlength > 3000 prints.
Example 4
Preparation of the DTR material
[0057] The DTR material was prepared as described in example 1 to 3.
Preparation of the heat-sensitive imaging element
[0058] To obtain a heat-sensitive imaging element according to the present invention, the
unexposed DTR material was developed for 12s at 24 °C in an aqueous alkaline solution
as described in example 1 to 3.
[0059] The initiated diffusion tranfer was allowed to continue for 18 s to form a silver
layer, whereafter the material was rinsed with water at 50 °C.
[0060] One of the thus obtained metallic silver layers was used as such, three other silver
layers were coated with a novolac layer of respectively 1, 2 and 5 g/m
2 Alnovol SPN452.
Exposing the heat-sensitive imaging element
[0061] The 4 materials were all imaged with a Gerber C42T™ internal drum platesetter at
12,000 rpm (367 m/s, pixel dwell time 0.032 µs) and 2540 dpi. The power level of the
laser in the image plane was 5.4 W.
[0062] After imaging, the plates were cleaned with a dry cotton pad and subsequently printed.
Printing the imagewise exposed element
[0063] The plate that did not get an extra coating layer after developing, showed strong
ablation during imaging and no residues were left on the exposed parts. The plates
with a novolac coating on top of 1 or 2 g/m
2 Alnovol SPN452, ablated as an easily removable yellow powder, while on the one with
a 5 g/m
2 novolac coating, still ablation residues were found after cleaning.
[0064] The plates were printed on a Heidelberg GTO46 printing machine with a conventional
ink (K+E) and a fountain solution of 5% G671c (commercially available from Agfa-Gevaert
N.V.) + 10% isopropanol.
[0065] The plate that did not get an extra coating layer after developing, did not show
any ink-uptake in the unexposed areas. All three layers with a novolac coating on
top, showed a good ink-uptake and a runlenght> 3000 prints .
1. A heat-sensitive imaging material for making lithographic printing plates comprising
on a lithographic base, having a hydrophilic surface, a metallic layer or metal oxide
layer and on top thereof an oleophobic polymeric layer having a thickness of less
than 5µm characterised in that said polymeric layer comprises a polymer containing
phenolic groups.
2. A heat-sensitive imaging material according to claim 1 wherein said polymer containing
phenolic groups is a phenolic resin or a hydroxyphenyl subsituted polymer.
3. A heat-sensitive imaging material according to claim 1 wherein said metallic layer
is a metallic silver or bismuth layer.
4. A heat-sensitive imaging material according to claim 1 wherein said metal oxide layer
is a titanium oxide layer.
5. A heat-sensitive imaging material according to claim 1 wherein said metallic layer
or metal oxide layer has a thickness between 0.05 and 1.5µm.
6. A heat-sensitive imaging material according to claim 1 wherein said lithographic base
having a hydrophilic surface is a grained and anodised aluminum support.
7. A heat-sensitive imaging material according to claim 6 wherein the lithographic base
having a hydrophilic surface is an anodized aluminum support which has been treated
with a compound selected from the group consisting of polyvinylphosphonic acid, polyvinylmethylphosphonic
acid, phosphoric acid esters of polyvinyl alcohol, polyvinylsulphonic acid, polyvinylbenzenesulphonic
acid, sulphuric acid esters of polyvinyl alcohol, and acetals of polyvinyl alcohols
formed by reaction with a sulphonated aliphatic aldehyde.
8. A heat-sensitive imaging material according to claim 1 wherein said lithographic base
having a hydrophilic surface comprises a plastic support provided with a hydrophilic
binder cross-linked by means of a hydrolysed tetra-alkylorthosilicate.
9. A method for making a lithographic printing plate comprising the step of image-wise
exposing to actinic radiation a heat-sensitive element comprising on a lithographic
base , having a hydrophilic surface, a metallic layer or metal oxide layer and on
top thereof an oleophobic polymeric layer having a thickness of less than 5µm characterised
in that said polymeric layer comprises a polymer containing phenolic groups.
10. A method for making multiple copies of an original comprising the steps of:
- image-wise exposing to actinic radiation a heat-sensitive imaging material comprising
on a lithographic base , having a hydrophilic surface, a metallic layer or metal oxide
layer and on top thereof an oleophobic polymeric layer having a thickness of less
than 5µm characterised in that said polymeric layer comprises a polymer containing
phenolic groups,
- starting printing without an additional wet treatment of the exposed imaging material.
11. A method according to claim 9 wherein said image-wise exposure is carried out by an
IR-laser.