BACKGROUND OF THE INVENTION
[0001] The present invention relates to a substrate for presensitized plate for use in making
a lithographic printing plate (hereinafter referred to as "PS plate") and hence for
lithographic printing plate and in particular, to a substrate for PS plate or lithographic
printing plate which can show improved suitability for a plate scanner of an ink-presetting
system.
[0002] The PS plate comprising an aluminum substrate is in general imagewise exposed to
light, developed with a developer and then subjected to retouching to give a lithographic
printing plate. The resulting printing plate is put on a printing press to perform
printing operations.
[0003] The basic principle of the offset printing is to express light and shade of patterns
in terms of the difference between the numbers of half-tone dots and, therefore, it
is ideal that the half-tone dot portion having a rate of area occupied by the half-tone
dots of 10% and solid portion printed on paper should have the same ink thickness.
Moreover, the amount of ink consumed during the offset printing depends on the area
occupied by patterns and correspondingly it is necessary to read the rate of area
occupied by the patterns for every key pitch of an ink bottle and to control the switching
(or opening and closing) of the ink key depending on the outputted value of the rate.
For this reason, an ink-presetting system is in general used for controlling the switching
of the ink key. The "ink-presetting system" herein means a system for reading the
rate of the area of a lithographic printing plate occupied by patterns for every key
pitch by a plate scanner prior to the fitting of the printing plate to a printing
press and for automatically controlling the switching of the ink key depending on
the rate observed. The application of such a system makes it possible to substantially
reduce the time required for adjusting the amount or thickness of ink and to improve
productivity.
[0004] The reading of the rate of area of a lithographic printing plate occupied by patterns
is generally carried out by the following method using a plate scanner. The method
comprises the steps of irradiating the plate surface with light from a light source
arranged perpendicularly to the scanning direction, detecting or determining the quantity
of light reflected from the surface of an aluminum plate on the non-image area by
photosensors arranged on a linear line parallel to the light source and calculating
the area occupied by light-absorbing image area to thus determine the rate of area
occupied by the patterns.
[0005] However, in case of lithographic printing plate comprising an aluminum plate as a
substrate, the following disadvantages are observed when reading the rate of the area
occupied by patterns. The aluminum plate has stripes (rolling marks) on the surface
along the rolling direction and hence the light incident upon the surface is scattered
within the planes perpendicular to the rolling marks. Thus, the light which is made
incident upon the aluminum plate perpendicularly to the rolling direction thereof
is scattered back and forth (parallel direction) relative to the direction of the
light propagation. Therefore, the quantity of light detected by a method capable of
detecting only the light within a limited angle of reflection is smaller than that
observed when any scattering by the rolling marks is not caused. On the other hand,
the light which is made incident upon the aluminum surface parallel to the rolling
direction thereof is scattered and spreads towards the directions perpendicular to
the direction of light propagation due to the presence of the rolling marks, but the
resulting quantity of light detected is almost the same as that observed for the aluminum
plate free of rolling marks if the quantities of light detected by all of the photosensors
are integrated, since many light sources are arranged in this direction.
[0006] As has been explained above, when reading the rate of the area of a lithographic
printing plate occupied by patterns using a plate scanner and putting the printing
plate on a printing press in such a manner that the rolling direction of the aluminum
plate of the printing plate is perpendicular to the direction of the vector component,
parallel to the substrate surface, of the incident light from the light source of
a plate scanner, the quantity of reflected light is lowered and, therefore, a rate
of area occupied by the patterns greater than the true value would be outputted from
the scanner.
[0007] To solve this problem, there have been proposed various methods for eliminating the
rolling marks remaining on the surface of an aluminum substrate. Examples of such
methods include those comprising surface roughening treatments, for instance, mechanical
methods such as brush graining and ball graining; and electrochemical methods such
as electrolytic graining; and a combination of these two methods. However, these treatments
make the manufacturing process complicated and lead to an increase in the production
cost.
[0008] Further, the rolling marks are masked by, for instance, dispersion of titanium oxide
powder in a light-sensitive layer and/or a primer layer for a lithographic printing
plate requiring no dampening water, but a large amount of titanium oxide must be dispersed
in the layers to mask the rolling marks and this makes the installation for dispersing
the same complicated and expensive.
SUMMARY OF THE INVENTION
[0009] An object of the present invention is to provide a substrate for PS plates or lithographic
printing plates which can provide a lithographic printing plate capable of outputting
the rate of area of the plate occupied by patterns almost equal to the true area occupied
by the patterns even if, when determining the rate of the area occupied by patterns
using a plate scanner of an ink presetting system, the lithographic printing plate
is put on a printing press in such a manner that the rolling direction of the aluminum
substrate of the printing plate is perpendicular to the direction of the vector component,
parallel to the substrate surface, of the incident light from light sources of the
plate scanner.
[0010] The inventors of this invention have conducted various studies to achieve the foregoing
object and have completed the present invention. Consequently, the present invention
relates to a substrate for lithographic printing plates which comprises an aluminum
plate whose specular gloss determined by making light incident upon the aluminum plate
perpendicularly to the rolling direction of the plate is at least 70% of that determined
by making light incident upon the plate parallel to the rolling direction.
DESCRIPTION OF THE PREFERRD EMBODIMENTS
[0011] The present invention will hereunder be explained in more detail on the basis of
preferred embodiments.
Substrate
[0012] The aluminum plate used in the present invention as a material for making the substrate
for lithographic printing plates must have the specular gloss determined by making
light incident upon the aluminum plate perpendicularly to the rolling direction of
the plate is at least 70% of that determined by making light incident upon the plate
parallel to the rolling direction.
[0013] The term "specular gloss" herein means the value G
s ( e ) represented by the following equation (I) and can be determined by, for instance,
Glossmeter VG-1 D available from Nippon Denshoku Kogyo K.K.
6 : angle of incident light (in the invention, the measurement was carried out at
a 0 of 600 )
φs: specular reflection light flux from the sample surface
φos: specular reflection light flux from the reference surface
Gs ( e ) : specular gloss
[0014] The aluminum plate used in the invention as a material for the substrate used for
lithographic printing plates is a plate-like material mainly comprising aluminum such
as those comprising pure aluminum or those comprising an aluminum alloy containing
a small amount of foreign atoms. Examples of the foreign atoms are silicon, iron,
manganese, copper, magnesium, chromium, zinc, bismuth, nickel and titanium. The content
of these foreign atoms in the aluminum alloys is in the order of up to about 10% by
weight. Aluminum preferably used in the present invention is pure aluminum, but it
is very difficult to produce completely pure aluminum from the viewpoint of the refining
technique. Therefore, preferably used are those comprising foreign atoms as low as
possible and the aluminum alloys having the foreign atom content defined above can
be used in the present invention as materials for preparing the substrate without
any problem. As explained above, the composition of the aluminum plates usable in
the present invention is not restricted to specific one and hence those obtained from
conventionally known or currently used materials can arbitrarily be employed.
[0015] The aluminum plate used in the invention is usually produced by the rolling technique
and in general has a thickness ranging from 0.1 to 0.5 mm. The specular gloss of the
aluminum plate is greatly dependent upon the rolling rolls used in the rolling process
and the rolling rolls are thus very important in the present invention. In particular,
the surface roughness of the rolling rolls is most important and preferably those
having an averaged central line surface roughness (R
a ) of not more than 0.1 µm, more preferably not more than 0.05 µm are used. The aluminum
plate obtained by rolling with rolls having such a surface roughness has a surface
roughness (R
a ) ranging from 0.1 to 0.01 /1.m.
[0016] If rolling rolls having a surface roughness of more than 0.1 µm are used, the specular
gloss determined by making light incident upon the aluminum plate perpendicularly
to the rolling direction of the plate is less than 70% of that determined by making
light incident upon the plate parallel to the rolling direction. Accordingly, if the
rate of area occupied by patterns is determined by a plate scanner, the plate scanner
outputs a value greater than the true rate and, therefore, the resulting aluminum
plate cannot be used in the present invention.
[0017] The aluminum plate thus obtained is degreased and then desired coating layers can
directly be applied thereto, but the surface of the plate may further be treated prior
to the application of the coating layers.
Surface Treatments
[0018] A rolling oil is adhered to the surface of the rolled aluminum plate and hence the
plate must be degreased. The degreasing treatment is performed by the use of an alkali
such as caustic soda, caustic potash, sodium carbonate, sodium phosphate and sodium
silicate. Preferred conditions for degreasing are a temperature ranging from 30 to
100° C, an alkali concentration ranging from 1 to 50% and a treating time ranging
from 1 to 100 seconds.
[0019] After such a degreasing treatment, coating layers such as a light-sensitive layer
may directly be applied to the aluminum plate, but the plate may be subjected to other
surface treatments such as graining, anodization and/or hydrophilization treatments
prior to the application of the coating layers. Preferred graining treatments are,
for instance, sand blasting or liquid honing methods in which an abrasive is blown
on the plate surface, a brush graining method in which the aluminum surface is rubbed
with a brush and wet abrasive particles and an electrolytic graining carried out in
an electrolyte such as nitric acid or hydrochloric acid, which may, if necessary,
be used in combination. The grained plate surface is cleaned with an acid or alkali
and then anodized. The anodization treatment is in general performed in an electrolyte
comprising sulfuric acid, but it may also be performed in an electrolyte such as those
comprising phosphoric acid or a mixed acid of sulfuric acid and phosphoric acid. Preferred
conditions for the anodization are not always particularly specified, but are in general
an electrolyte concentration ranging from 1 to 30% by weight, a temperature ranging
from 20 to 50 C, an anodization time ranging from 5 to 100 seconds and a current density
ranging from 5 to 100 A/dm
2.
[0020] After forming a desired anodized layer, the aluminum plate may be hydrophilized by
immersing it into a sodium silicate solution. Other hydrophilization treatments may
also be used and examples thereof are immersion in a fluorozirconate solution, a polyacrylate
solution and a polyvinylphosphonate solution. Preferred conditions for the hydrophilization
treatment are a concentration ranging from 1 to 20% by weight, a temperature ranging
from 20 to 80 ° C and a treating time ranging from 5 to 30 seconds.
[0021] Various kinds of lithographic printing plates can be prepared by applying a variety
of layers onto the surface of the thus treated aluminum substrate of the present invention
for use in making lithographic printing plates.
[0022] Specific examples of such lithographic printing plates will be described below, but
the present invention is by no means limited to these specific examples.
[I] PS Plate
[0023] PS plates comprise a substrate provided thereon with a light-sensitive layer. The
light-sensitive layer is imagewise exposed to light directly through an original or
through a film by the usual photomechanical method. Thereafter, the imagewise exposed
light-sensitive layer is developed with a developer such as an organic solvent or
an alkali solution to thus give ink-receptive image portions and hydrophilic non-image
portions to hence give a lithographic printing plate.
[0024] The light-sensitive layer may be obtained from various kinds of light-sensitive composition.
Specific examples thereof will be described below, but the present invention is by
no means limited to these specific examples.
(1) Light-sensitive Layer Comprising Diazo Resin and Binder
[0025] Preferred examples of negative-working light-sensitive diazo compounds useful in
the invention are such a reaction product of a diazonium salt with an organic condensation
agent having reactive carbonyl group, e.g., aldol or acetal as a condensation product
of diphenylamine-p-diazonium salt and formaldehyde (so-called light-sensitive diazo
resins) disclosed in U.S.Patent Nos. 2,063,631 and 2,667,415. Examples of other useful
condensed diazo compounds are such as those disclosed in U.S. Patent No. 3,679,419
and U.K. Patent Nos. 1,312,925 and 1,312,926. The light-sensitive diazo compounds
of this type are in general available in the form of water-soluble inorganic salts
and therefore, they can be applied as an aqueous solution. Alternatively, it is also
possible to use substantially water-insoluble light-sensitive diazo resins obtained
by reacting these water-soluble diazo compounds with aromatic or aliphatic compounds
having either one or both of at least one phenolic hydroxyl group and sulfonic acid
group in the manner as disclosed in U.K. Patent No. 1,280,885.
[0026] In addition, they may be used as a reaction product with hexafluorophosphates or
tetrafluoroborates as disclosed in J.P. KOKAI No. 56-121031. Besides, diazo resins
as disclosed in U.K. Patent No. 1,312,925 are also preferred in the present invention.
[0027] Examples of the compounds having phenolic hydroxyl group are hydroxybenzophenone,
4,4-bis-(4'hydroxyphenyl)pentanoic acid, resorcinol, and diphenolic acids such as
diresorcinol, which may have substituents other than the phenolic hydroxyl group.
The term "hydroxybenzophenone is herein defined to include 2,4-dihydroxybenzophenone,
2-hydroxy-4-methoxybenzophenone, 2,2'-dihydroxy-4,4'dimethoxybenzophenone and 2,2',4,4'-tetrahydroxybenzophenone.
Examples of preferred sulfonic acids include aromatic sulfonic acids such as sulfonic
acids of benzene, toluene, xylene, naphthalene, phenol, naphthol and benzophenone
or soluble salts thereof such as ammonium salts and alkali metal salts. The compounds
having a sulfonate group may in general be substituted with a lower alkyl group, a
nitro group, a halo group, and/or another sulfonate groups. Preferred examples thereof
are benzenesulfonic acid, toluenesulfonic acid, naphthalenesulfonic acid, 2,5-dimethylbenzenesulfonic
acid, sodium benzenesulfonate, naphthalene-2-sulfonic acid, 1-naphthol-2 (or 4)-sulfonic
acid, 2,4-dinitro-1-naphthol-7-sulfonic acid, 2-hydroxy-4-methoxybenzophenone-5-sulfonic
acid, sodium m-(p'-anilinophenylazo)benzenesulfonate, alizarin- sulfonic acid, o-toluidine-m-sulfonic
acid and ethanesulfonic acid. Sulfuric acid esters of alcohols or aromatic hydroxy
compounds or salts thereof are also preferably used. These compounds are usually available
as anionic surfactants. Specific examples thereof are ammonium salts or alkali metal
salts of lauryl sulfate, alkylaryl sulfates, p-nonylphenyl sulfate, 2-phenylethyl
sulfate and isooctylphenoxy diethoxyethyl sulfate.
[0028] These substantially water-insoluble light-sensitive diazo resins can be isolated
as precipitates by mixing an aqueous solution of a water-soluble light-sensitive diazo
resin and approximately the same amount of an aqueous solution of the foregoing aromatic
or aliphatic compound.
[0029] In addition, preferred are also include diazo resins disclosed in U.K. Patent No.
1,312,925.
[0030] The most preferred diazo resin is 2-methoxy-4-hydroxy-5-benzoylbenzenesulfonate of
a condensate of p-diazodiphenylamine and formaldehyde.
[0031] The content of the diazo resin in the light-sensitive layer preferably ranges from
5 to 50% by weight. As the content thereof is lowered, the light sensitivity of the
resulting light-sensitive layer is correspondingly increased, but in contrast therewith,
the stability with time thereof is lowered. The optimum content of the diazo resin
ranges from about 8 to 20% by weight.
[0032] On the other hand, various polymeric compounds may be used as the binder of the light-sensitive
composition, but in the present invention, preferably used are those carrying hydroxyl,
amino, carboxyl, amido, sulfonamido, active methylene, thioalcohol and/or epoxy groups.
Specific examples of the binders include schellac as disclosed in U.K. Patent No.
1,350,521; polymers mainly comprising hydroxyethyl acrylate units or hydroxyethyl
methacrylate units as disclosed in U.K. Patent No. 1,460,978 and U.S. Patent No. 4,123,276;
polyamide resins as disclosed in U.S. Patent No. 3,751,257; phenol resins and polyvinyl
acetal resins such as polyvinyl formal resins and polyvinyl butyral resins disclosed
in U.K. Patent No. 1,074,392; linear polyurethane resins disclosed in U.S. Patent
No. 3,660,097; polyvinyl alcohol resins which are converted into phthalates, epoxy
resins obtained by the condensation of bisphenol A and epichlorohydrin, polymers having
amino groups such as polyaminostyrene and polyalkylamino(meth)acrylate, and cellulose
derivatives such as cellulose acetate, cellulose alkyl ether and cellulose acetate
phthalate.
[0033] The light-sensitive composition comprising a diazo resin and a binder may further
comprise other additives such as a pH indicator as disclosed in U.K. Patent No. 1,041,463;
and phosphoric acid and dyes as disclosed in U.S. Patent No. 3,236,646.
(2) Light-Sensitive Composition Comprising o-Quinonediazide Compound
[0034] Particularly preferred o-quinonediazide compounds are, for instance, o-naphthoquinonediazide
compounds which are disclosed in a variety of publications, for instance, U.S. Patent
Nos. 2,766,118; 2,767,092; 2,772,972; 2,859,112; 2,907,665; 3,046,110; 3,046,111;
3,046,115; 3,046,118; 3,046,119; 3,046,120; 3,046,121; 3,046,122; 3,046,123; 3,061,430;
3,102,809; 3,106,465; 3,635,709; and 3,647,443 and which are preferably used in the
composition. Among these, preferred are o-naphthoquinonediazidosulfonic acid esters
or o-naphthoquinonediazidocarboxylic acid esters of aromatic hydroxy compounds; o-naphthoquinonediazidosulfonic
acid amides or o-naphthoquinonediazidocarboxylic acid amides of aromatic amino compounds
and particularly, esterification reaction products of condensates of pyrogallol and
acetone with o-nap hthoquinonediazidosulfonic acid disclosed in U.S. Patent No. 3,635,709;
esterification reaction products of polyesters having hydroxyl groups at the ends
with o-napht hoquinonediazidosulfonic acid or o-naphthoquinon ediazidocarboxylic acid
disclosed in U.S. Patent No. 4,028,111; esterification reaction products of homopolymers
of p-hydroxystyrene or copolymers of p-hydroxystyrene and monomers copolymerizable
therewith, with o-naphthoquinonediazidosulfonic acid or o-naphthoquinonediazidocarboxylic
acid disclosed in U.K. Patent No. 1,494,043; amidation reaction products of copolymers
of p-aminostyrene and monomers copolymerizable therewith, with o-naphthoquinonediazidosulfonic
acid or o-naphth oquinonediazidocarboxylic acid disclosed in U.K. Patent No. 3,759,711
are very preferable.
[0035] These o-quinonediazide compounds may be used alone, but are preferably used in combination
with alkali-soluble resins. Preferred alkali-soluble resins include novolak type phenol
resins and specific examples thereof are phenol-formaldehyde resins, o-cresol-formaldehyde
resins, and m-cresol-formaldehyde resins. Moreover, it is more preferable to use condensates
of phenols or cresols substituted with an alkyl group having 3 to 8 carbon atoms with
formaldehyde such as t-butylphenol-formaldehyde resin simultaneously with the foregoing
phenol resins as disclosed in U.S. Patent No. 4,123,279. The composition for forming
the light-sensitive layer may comprise these alkali-soluble resins in an amount ranging
from about 50 to about 85% by weight, preferably 60 to 80% by weight on the basis
of the total weight of the composition.
[0036] The light-sensitive composition comprising o-quinonediazide compounds may, if necessary,
comprise other components such as dyes, plasticisers and compounds capable of imparting
printing out properties to the resulting light-sensitive layer as disclosed in U.K.
Patent Nos. 1,401,463 and 1, 039,475 and U.S. Patent No. 3,969,118.
(3) Light-sensitive Layer Obtained from Composition Comprising Polymer Having Carboxylic
Acid or Carboxylic Acid Anhydride Residues, Addition-polymerizable Unsaturated Compound
and Photopolymerization Initiator
[0037] The lithographic printing plate which comprises a substrate provided with a layer
of the composition comprising a polymer having carboxylic acid residues or carboxylic
anhydride residues, an addition-polymerizable unsaturated compound and a photopolymerization
initiator is excellent in storability, the exposed aluminum plate surface on the non-image
area is hardly contaminated with a printing ink, has good hydrophilicity capable of
rapidly removing ink stains on the non-image area and the aluminum plate has high
adhesion to the light-sensitive layer.
[0039] In the general formulas (A) to (D), R
1 and R
4 each represents a hydrogen atom or an alkyl group; R
3 represents a phenylene group or an alkylene group optionally having a hydroxyl group;
R
5 represents a hydrogen atom or an alkyl group optionally having substituents; R
6 represents an alkyl, allyl, aryl or cycloalkyl group which may have substituents;
and n is an integer of 0 or 1.
[0040] More specifically, examples of the repeating units represented by formula (A) are
those derived from acrylic acid, methacrylic acid, crotonic acid and vinyl benzoic
acid; examples of the repeating units represented by formula (B) those derived from
maleic acid, maleic acid monohydroxyalkyl ester and maleic acid monocyclohexyl ester;
examples of the repeating units of formula (C) those derived from maleic acid monoalkylamide
and maleic acid monohydroxyalkylamide; and examples of the repeating units represented
by formula (D) those derived from maleic anhydride and itaconic anhydride. As the
polymers, those having an average molecular weight ranging from 1,000 to 100,000 are
usually used in the invention.
[0041] The addition polymerizable unsaturated compounds herein mean monomers having ethylenically
unsaturated double bonds which can cause addition polymerization between them in the
three-dimensional direction when the photopolymerizable light-sensitive composition
is irradiated with actinic rays. Examples thereof are unsaturated carboxylic acids,
esters of unsaturated carboxylic acids and aliphatic polyhydric compounds and esters
of unsaturated carboxylic acids and aromatic polyhydric compounds.
[0042] As the photopolymerization initiators, there may be mentioned, for instance, benzoin,
benzoin alkyl ether, benzophenone, anthraquinone and Michler's ketones which may be
used alone or in combination in an amount ranging from 1 to 3 g/m
2 (weighed after drying).
[II] Presensitized Plate for Use in Making Lithographic Printing Plate Requiring No
Dampening Water (Hereunder Refered to as "PS Plate Requiring No Dampening Water")
[0043] There have already been proposed various PS plates requiring no dampening water in
which a silicone rubber layer serves as a non-image area (see, for instance, Japanese
Examined Patent Publication (hereinafter referred to as "J.P. KOKOKU") Nos. Sho 44-23042,
Sho 46-16044, Sho 54-26923 and Sho 61-54222 and Japanese Unexamined Patent Publication
(Hereinafter referred to as "J.P. KOKAI") No. Sho 63-265247).
[0044] There are two kinds of methods for preparing a PS plate requiring no dampening water
of this type. One of these is disclosed in, for instance, J.P. KOKOKU No. Sho 46-16044
in which image areas are formed by dissolving the light-sensitive layer on the image
areas with a developer to thus remove the silicone rubber layer on the image areas
and the other is disclosed in, for instance, J.P. KOKOKU No. Sho 54-26923 and J.P.
KOKAI No. 56-80046 in which a PS plate requiring no dampening water comprising a photoadhesive
or photopeelable light-sensitive layer and a silicone rubber layer is employed and
the silicone rubber layer on image areas is selectively removed.
[0045] In the former, i.e., in the method wherein the image areas are formed by dissolving
the light-sensitive layer on the image areas with a developer, it is preferred to
apply a silicone rubber layer having a thickness ranging from 0.5 to 5 /1.m on the
photopolymerizable light-sensitive layer of the foregoing polymer having carboxylic
acid residues or carboxylic acid anhydride residues, an addition-polymerizable unsaturated
compound and a photopolymerization initiator.
[0046] If the latter and in particular, a PS plate requiring no dampening water which comprises
a photoadhesive light-sensitive layer and a silicone rubber layer is exposed to light,
the photoadhesive light-sensitive layer is firmly photolytically adhered to the silicone
rubber layer. Thus, making the most use of this phenomenon, only the silicone rubber
layer on the non-exposed areas can be selectively peeled off and removed with a developer
which does not substantially dissolve the photoadhesive light-sensitive layer (only
slightly dissolves the layer) and is capable of swelling the light-sensitive layer
and/or the silicone rubber layer. The exposed light-sensitive layer thus serves as
an ink-receptive portion of the printing plate. In this case, the silicone rubber
layer is preferably applied onto the light-sensitive layer comprising a component
substantially insoluble in a developer, an addition-polymerizable unsaturated compound
and a photopolymerization initiator in a thickness ranging from 0.5 to 5 /1.m.
[0047] The effect of the present invention is particularly conspicuous in this embodiment,
i.e., in the PS plate requiring no dampening water, since the surface of the aluminum
substrate is not generally subjected to any surface roughening treatment (the rolling
marks are reduced or disappeared through the surface roughening treatment).
[III] PS Plate for Electrophotographic Plate-Making Process
[0048] The electrophotographic plate making method has been known and is detailed in "DENSHI
SHASHIN GIJUTSU NO KISO TO OYO (The Basis and Applications of Electrophotographic
Techniques), issued by Society of Electrophotography, published by Corona Publishing
Company (1988) of "KIROKU ZAIRYO MANUAL (A Manual of Recording Materials", Trykepus
Publishing Company (1981) which may be used in the invention.
[0049] For instance, there has been known a method which comprises applying, onto an aluminum
substrate, a photoconductive layer comprising at least a photoconductive material
and an alkali-soluble resin, developing with a toner, fixing the toner and then removing
the photoconductive layer on non-image area free of toner with an alkaline solution
in the usual manner to give a lithographic printing plate.
[0050] Specific examples thereof are those disclosed in J.P. KOKOKU Nos. Sho 37-17162, Sho
38-6961, Sho 38-7758, Sho 41-2426 and Sho 46-39405 and J.P. KOKAI Nos. Sho 50-19509,
Sho 50-19510, Sho 52-2437, Sho 54-145538, Sho 54-134632, Sho 55-105254, Sho 55-153948,
Sho 55-161250, Sho 57-147656 and Sho 57-161863.
[0051] Moreover, it is also possible to use a method which comprises transferring the toner
image formed on an electrophotographic light-sensitive material onto a proper substrate
to give a lithographic printing plate.
[0052] For instance, toner images are formed on an organic or inorganic electrophotographic
light-sensitive material in the usual manner. The resulting toner images are transferred
to an aluminum substrate in the usual known transfer method such as a corona transfer,
bias-roller transfer or pressure transfer method to give a lithographic printing plate.
In addition, the toner images can, if necessary, be transferred to an aluminum substrate
after a plurality of transferring processes through a transferring material such as
a rubber roller.
[0053] Further, a lithographic printing plate may also be prepared by previously applying
an insulating layer onto an aluminum substrate, then transferring toner images to
the insulating layer in the usual manner and removing the non-image area free of toner.
[0054] This method is detailed in, for instance, J.P. KOKAI Nos. Sho 59-36272, Sho 60-107042,
Sho 61-118778, Hei 1-225975 and Hei 1-216367 and J.P. KOKOKU No. Sho 55-42752.
[0055] The lithographic printing plate obtained from the substrate therefor of the present
invention can output the rate of area of the printing plate occupied by patterns almost
equal to the true area of the patterns formed thereon even if, when determining the
rate of the area occupied by patterns using a plate scanner of an ink presetting system,
the lithographic printing plate is put on a printing press in such a manner that the
rolling direction of the aluminum substrate of the printing plate is perpendicular
to the direction of the vector component, parallel to the substrate surface, of the
incident light from light sources of the plate scanner.
[0056] The present invention will be explained in more detail with reference to the following
non-limitative working Examples and the effect practically attained by the present
invention will also be discussed in detail in comparison with Comparative Examples.
Example 1
[0057] An aluminum plate (JIS A1050; surface roughness = 0.04 µm) which had been rolled
with rolls having an averaged center line surface roughness (Ra) of 0.03 µm was immersed
in a 10% aqueous solution of NaOH at 50 C for 20 seconds to remove the rolling oil
from the surface thereof and then immersed in a 2.5% aqueous solution of No. 3 sodium
silicate at 70 °C for 10 seconds to give an aluminum substrate.
[0058] The rate of specular gloss of the foregoing rolled aluminum plate (JIS A1050) was
determined by a glossmeter VG-1 D available from Nippon Denshoku Kogyo K.K. The results
thus obtained are summarized in the following Table 1. The rate of specular gloss
is defined as follows:
Rate of Specular Gloss(%) = (S.G.)v x 100/(S.G.)p
(S.G.)v : specular gloss determined by making light incident upon the surface vertically to
the rolling direction.
(S.G.)p : specular gloss determined by making light incident upon the surface parallel
to the rolling direction.
[0059] A light-sensitive layer was formed on the surface of the aluminum substrate thus
obtained by applying a light-sensitive solution having the following composition in
an amount of 2.0 g/m
2(weighed after drying) and then drying.

[0060] The PS plate thus prepared was imagewise exposed to light in a vacuum printing frame
by making the surface of the plate and an original having a rate of area occupied
by half-tone dots of 50% at a density of 133 lines/inch and then irradiating the assembly
with light from a 3 KW metal halide lamp for 50 seconds at a distance of 1 m, then
developed with a developer having the following composition and gummed-up with an
aqueous solution of gum arabic to give a lithographic printing plate.

[0061] The resulting lithographic printing plate was subjected to test for examining suitability
for plate scanner of an ink presetting system. The results obtained are summarized
in Table 1.
[0062] The term "suitability for plate scanner" herein means the ability of outputting the
rate of area of a lithographic printing plate occupied by patterns almost equal to
the true area occupied by the patterns even if the lithographic printing plate is
put on a printing press in such a manner that the rolling direction of the aluminum
substrate of the printing plate is perpendicular to the direction of the vector component,
parallel to the substrate surface, of the incident light from the light source of
the plate scanner. Therefore, the smaller the difference between the rates of the
area occupied by patterns each observed when the rolling direction is perpendicular
to or parallel to the direction of the vector component, parallel to the substrate
surface, of the incident light, the higher the suitability for plate scanner.
Comparative Example 1
[0063] An aluminum plate (JIS A1050; surface roughness = 0.20 µm) which had been rolled
with conventional rolls having an averaged center line surface roughness of 0.2 µm
was immersed in a 10% aqueous solution of NaOH at 50 C for 20 seconds to remove the
rolling oil from the surface thereof and then immersed in a 2.5% aqueous solution
of No. 3 sodium silicate at 70 ° C for 10 seconds to give an aluminum substrate.
[0064] The rate of specular gloss of the foregoing rolled aluminum plate (JIS A1050) was
determined in the same manner used in Example 1. The results thus obtained are summarized
in Table 1.
[0065] The suitability for plate scanner of the lithographic printing plate produced in
the same manner used in Example 1 was likewise determined and the results obtained
were summarized in Table 1.
Example 2
[0066] To an aluminum substrate prepared in the same procedures used in Example 1, there
were applied, in order, a primer layer, a light-sensitive layer and a silicone rubber
layer in the following manner to give an original PS plate requiring no dampening
water.
o Primer Layer
[0067] The primer layer was formed by applying a composition for primer layer having the
following composition onto the surface of the resulting aluminum substrate in an amount
of 8.0 g/m
2 (weighed after drying) and then heating at 120° C for 3 minutes to dry the same.
Composition for Primer Layer
[0068] A solution comprising 450 parts by weight of pure water and 2.6 parts by weight of
anhydrous sodium carbonate was heated to 70 C and 50 parts by weight of casein powder
(casein lactate (New Zealand- grown product; available from Murray Coulburn Cooperative
Co., Ltd.)) was added to and dissolved in the solution with stirring and then the
following components were incorporated into the aqueous casein solution to give a
composition for primer layer:

o Light-Sensitive Layer
[0069] Then a light-sensitive layer was formed on the resulting primer layer by applying
a light-sensitive composition having the following composition in an amount of 3.0
g/m
2 (weighed after drying) and drying at 100°C for one minute.

o Silicone Rubber Layer
[0070] A silicone rubber layer was formed on the resulting light-sensitive layer by applying
a composition for silicone rubber layer having the following composition in an amount
of 2.0 g/m
2 (weighed after drying) and then drying at 140°C for 2 minutes to harden the layer.

[0071] A one-side matted polypropylene film having a thickness of 9 /1.m was laminated with
the surface of the silicone rubber layer thus produced to give an original PS plate
requiring no dampening water.
[0072] The original PS plate requiring no dampening water thus prepared was imagewise exposed
to light in a vacuum printing frame by making the surface of the plate come in close
contact with an original having a rate of area occupied by half-tone dots of 50% at
a density of 133 lines/inch and then irradiating the assembly with light from a 3
KW metal halide lamp for 50 seconds at a distance of 1 m, then the laminate film was
peeled off, the exposed PS plate was developed by immersing, for one minute, in a
developer which comprised 12 parts by weight of benzyl alcohol, 5 parts by weight
of sodium iso propylnaphthalenesulfonate, one part by weight of triethanolamine and
82 parts by weight of water and then rubbed with a developing pad to remove the light-sensitive
layer and the silicone rubber layer on the non-exposed areas to thus give a lithographic
printing plate requiring no dampening water.
[0073] The suitability for plate scanner of the resulting printing plate was determined.
The results thus obtained are listed in Table 1 below.
Comparative Example 2
[0074] To an aluminum substrate prepared in the same manner used in Comparative Example
1, there were applied, in order, a primer layer, a light-sensitive layer and a silicone
rubber layer and the resulting original PS plate requiring no dampening water was
imagewise exposed to light and developed in the same manner used in Example 2 to give
a lithographic printing plate requiring no dampening water.
[0075] The suitability for plate scanner of the resulting printing plate was determined.
The results thus obtained are listed in Table 1 below.

[0076] This is a value obtained by imagewise exposing a PS plate to light through an original
having a rate of area occupied by half-tone dots of 50% at a density of 133 lines/inch
and determining the rate of area on the plate occupied by the half-tone dots using
a plate scanner (Demia 640; available from Dainippon Ink & Chemicals, Incorporated).
[0077] *2: The rate of area occupied by the half-tone dots observed when the lithographic
printing plate was put on a printing press in such a manner that the rolling direction
of the aluminum substrate of the plate is perpendicular to the direction of the vector
component, parallel to the substrate surface, of the incident light from the light
source of the plate scanner.
[0078]
