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(11) | EP 0 441 502 A2 |
| (12) | EUROPEAN PATENT APPLICATION |
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| (54) | Lithographic plate finisher |
| (57) A non-emulsion type plate finisher which comprises a solvent whose solubility in
water at 20°C is not more than 5 % by weight. The plate finisher is excellent in the
desensitizing ability and does not deteriorate the ink receptivity of image areas.
The lithographic printing plate to which the plate finisher is applied has good ink
receptivity from the beginning of the printing operation. The plate finisher is excellent
in stability over time and can be prepared easily with an inexpensive equipment. |
BACKGROUND OF THE INVENTION
[0002] Upon manufacturing a lithographic printing plate, a gumming up step is performed as the final process. In the gumming up step, a protecting agent, i.e., so-called desensitizing gum is applied onto the surface of the printing plate. This is applied to the plate for the purposes of preventing adhesion of contaminants on the plate after the plate is manufactured and till the plate is set on a printing press to thereby prevent occurrence of background contamination on printed matters and for preventing the formation of defects on the plate surface during storing the plates in the heaped up state or upon hitting them against a foreign substance. The most important purpose of the gumming up step is to prevent the lowering of the hydrophilic properties of non-image areas due to oxidization encountered when the plate surface is directly exposed to air and to enhance the hydrophilic properties thereof. For these reasons, the gumming up is a step indispensable for the plate making process.
[0003] As a gumming solution, there has been used, for a long time, a composition comprising an aqueous solution of gum arabic having a concentration ranging from about 15 to 30% by weight to which additives such as surfactants, pH-adjusting agents and preservatives are optionally added.
[0004] However, the desensitizing ability of gum arabic is so strong that the ink receptivity of image areas is often lowered. Therefore, it is sometimes observed that many unacceptale printed matters are formed till those having satisfactory ink concentration are surely obtained during printing operations.
[0005] There has been proposed an emulsion gum solution comprising an oil phase containing a lipophilic surfactant, such as an organic solvent soluble lipophilic surfactant, dissolved in a petroleum fraction and a water phase containing a water soluble organic high molecular compound dissolved therein. In such emulsion gum solution, gum arabic serves as not only a desensitizing agent but also a protective colloid to stabilize the emulsion.
[0006] However, gum arabic is a natural substance which is produced only in limited regions in the world and its amount of harvest is greatly influenced by various factors such as the climate at the regions. Thus the stable supply thereof is not always expected.
[0007] Under such circumstances, many attempts have been directed to the use of a variety of water-soluble polymeric compounds as desensitizing gum lithographic plate finishers instead of gum arabic.
[0008] For instance, Japanese Patent Un-examined Publication (hereunder referred to as "J.P. KOKAI") No. Sho 54-97102 (B.P. 2010298) discloses dextrin, sterabic, arabogalactan, alginic acid salts, polyacrylic acids, hydroxyethyl cellulose, polyvinyl pyrrolidone, polyacrylamide, methyl cellulose, hydroxypropyl cellulose, hydroxymethyl cellulose and salts of carboxyalkyl celluloses. Moreover, Japanese Patent Publication for Opposition Purpose (hereunder referred to as "J.P. KOKOKU") No. Sho 54-41921 discloses pullulan and pullulan derivatives; J.P. KOKAI No. Sho 58-197091 discloses polyvinyl pyrrolidone; and J.P. KOKAI No. Sho 56-133193 (U.S.P. 4,349,391) discloses polyvinyl alcohols. J.P.KOKAI No. Sho 59-57242 discloses modified starch derivatives which include roasted starch such as British gum, enzyme-modified dextrin such as enzyme dextrin and Schardinger dextrin, acid-treated starch such as solubilized starch, oxidized starch such as dialdehyde starch, gelatinized starch such as modified or non-modified gelatinized starch, esterified starch such as phosphoric acid starch, fatty acid starch, sulfuric acid starch, nitric acid starch, xanthogenic acid starch and carbamic acid starch, etherified starch such as carboxyalkylated starch, hydroxyalkylated starch, sulfoalkylated starch, cyanoethylated starch, allylated starch, benzylated starch, carbamylethylated starch and dialkylamino starch, crosslinked starch such as methylol crosslinked starch, hydroxyalkyl crosslinked starch, phosphoric acid crosslinked starch and dicarboxylic acid crosslinked starch, and starch graft copolymer such as starch polyacrylamide copolymer, starch polyacrylic acid copolymer, starch polyvinyl acetate copolymer, starch polyacrylnitrile copolymer, cationic starch polyacrylate copolymer, cationic starch polyvinyl compound copolymer, starch styrene maleic acid copolymer and starch polyethylene oxide copolymer.
[0009] However, all the plate finishers using water soluble organic polymeric compounds instead of gum arabic are inferior in the ability to desensitize non-image areas to that of gum arabic and therefore, if they are used as emulsion type gum solutions, the oil phase components often contaminate non-image areas.
[0010] Further, the water-soluble organic polymeric compounds are inferior in the property of protective colloid to gum arabic and therefore, emulsion type gum solutions using the polymeric compounds undergo phase separation into oil and aqueous phases in a few days.
[0011] Moreover, an expensive machine such as a homogenizer and labors are required to prepare an emulsion tupe gum solution.
[0012] To make up for these disadvatages, a non-emulsion type gum solution has been known. However, as explained earlier, the non-emulsion type gum solution using a large amount of gum arabic has disadvantages in that it is inferior in ink receptivity in image areas and that gum arabic is not stably supplied. On the other hand, a non-emulsion type gum solution containing a water-soluble organic polymeric compound instead of gum arabic is sufficient in the ability of preventing contamination in non-image areas because it does not contain a lipophilic component, but it is insufficient in ink receptivity in image areas so that many unacceptable printed matters are produced at the beginnig of printing operation.
SUMMARY OF THE INVENTION
[0013] Accordingly, an object of the present invention is to provide a lithographic plate finisher (hereunder referred to as "plate finisher") having good ability of desensitizing non-image areas but not reducing ink receptivity of image areas.
[0014] Another object of the present invention is to provide a plate finisher which is stable against phase separation even when the amount of gum arabic used is small.
[0015] A further object of the present invention is to provide a plate finisher which can easily be prepared with an inexpensive machine.
[0016] The foregoing objects can be quite effectively attained by a non-emulsion type plate finisher for lithographic printing plates which comprises a solvent whose solubility in water at 20 °C is not more than 5 % by weight.
DETAILED EXPLANATION OF THE INVENTION
SOLVENTS
[0018] The plate finisher of the present invention is characterized in that it comprises a solvent whose solubility in water at 20 °C is not more than 5 % by weight. The addition of such solvent improves ink receptivity of image areas.
[0019] Examples of such solvent include benzyl alcohol, ethylene glycol dibutyl ether, ethylene glycol benzyl ether, ethylene glycol monophenyl ether, hexyl glycol, hexyl diglycol, propyl propylene diglycol, methyl phenyl carbitol, diethylene glycol dibutyl ether, n-amyl alcohol, metyl amyl alcohol, isophorone, methyl cyclohexanone and acetophenone. Among them, benzyl alcohol is most preferred because it is highly stable and inexpensive but does not give out strong odor.
[0020] In the invention, the solvent may be used alone or in combination. The amount of the solvent used is preferably 0.1 to 10 % and more preferably 0.5 to 5 % by weight based on the total weight of the plate finisher. If it is less than 0.1 % by weight, ink receptivity of image areas is reduced. On the other hand, if it exceeds 10 % by weight, the plate surface becomes sticky and the drying property is deteriorated. Solvents whose solubility in water is more than 5 % by weight have no or insufficient effect on the prevention of lowering of ink receptivity of image areas.
WATER-SOLUBLE RESINS
[0022] Examples of such resins include natural high molecular compounds such as starches derived from sweet potato, potato, tapioca, wheat, corn and waxy corn; those derived from sea weeds such as carrageenan, laminaran, sea weed mannan, funori (a glue plant), Irish moss, agar and sodium alginate; mucilage derived from plants such as tororo-aoi mucin, mannan, quince seed mucin, pectin, tragacanth gum, karaya gum, xanthine gum, guar bean gum, locust bean gum, gum arabic, carob gum and benzoiun gum; mucilage derived from microorganisms such as homopolysaccharides (e.g., dextran, glucan and levan) and heteropolysaccharides (e.g., succinoglucan and xanthane gum); proteins such as glue, gelatin, casein and collagen; semisynthetic sompounds such as propylene glycol alginate and cellulose derivatives such as viscose, methyl cellulose, ethyl cellulose, methyl ethyl cellulose, hydroxyethyl cellulose, carboxymethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose and hydroxypropyl methyl cellulose phthalate; processed starches such as roasted dextrin (e.g., white dextrin, yellow dextrin and British gum), enzyme-modified dextrin such as enzyme dextrin and Schardinger dextrin, acid-treated starch such as solubilized starch, oxidized starch such as dialdehyde starch, gelatinized starch such as modified or non-modified gelatinized starch, esterified starch such as phosphoric acid starch, fatty acid starch, sulfuric acid starch, nitric acid starch, xanthogenic acid starch, carbamic acid starch and succinic acid starch, etherified starch such as carboxyalkylated starch, hydroxyalkylated starch, sulfoalkylated starch, cyanoethylated starch, allylated starch, benzylated starch, carbamylethylated starch and dialkylamino starch, crosslinked starch such as methylol crosslinked starch, hydroxyalkyl crosslinked starch, phosphoric acid crosslinked starch and dicarboxylic acid crosslinked starch, and starch graft copolymer such as starch polyacrylamide copolymer, starch polyacrylic acid copolymer, starch polyvinyl acetate copolymer, starch polyacrylnitrile copolymer, cationic starch polyacrylate copolymer, cationic starch polyvinyl compound copolymer, starch styrene maleic acid copolymer and starch polyethylene oxide copolymer; and synthetic compounds such as polyvinyl alcohol, modified polyvinyl alcohol such as partial acetal of polyvinyl alcohol, allyl modified polyvinyl alcohol, polyvinyl methyl ether, polyvinyl ethyl ether and polyvinyl isobutyl ether, poly(meth)acrylic acid derivatives such as sodium polyacrylate, partially saponified polyacrylate, partially saponified product of acrylate copolymer, salt of polymethacrylate and polyacrylamide, polyethylene glycol, polyethylene oxide, polyvinyl pyrrolidone, polyvinyl pyrrolidone-vinyl acetate copolymer, carboxy vinylpolymer, styrene-maleic acid copolymer and styrene-crotonic acid copolymer.
[0023] These water-soluble resins may be used in the plate finisher of the present invention alone or in combination in an amount of, preferably, 5 to 40 %, more preferably 10 to 30 % by weight based on the total weight of the plate finisher.
[0024] In the present invention, it is possible to significantly lower the amount of gum arabic to be used in the plate finisher. Although gum arabic may not be used at all in the finisher, it is preferable to use gum arabic in an amount of 1 to 20 % by weight based on the total weight of the water-soluble resin used in the finisher to give sufficient desensitizing ability to non-image areas.
pH ADJUSTING AGENTS
[0025] In general, the plate finisher is preferably used in the acid region, i.e., at pH ranging from 2 to 6. The pH value is generally adjusted by adding a mineral acid, an organic acid, an inorganic salt, an alkali agent or the like to the plate finisher. The amount thereof generally ranges from 0.01 to 3 % by weight.
[0026] Useful examples of the foregoing mineral acids are nitric acid, sulfuric acid and phosphoric acid and those of the organic acids are citric acid, acetic acid, oxalic acid, malonic acid, p-toluenesulfonic acid, tartaric acid, malic acid, lactic acid, levulinic acid, phytic acid, benzoic acid, butyric acid, maleic acid, picolinic acid and organophosphonic acids .
[0027] Useful examples of the foregoing inorganic salts are water soluble alkali metal salts and ammonium salts of nitric acid, phosphoric acid, sulfuric acid, molybdenic acid, acetic acid, polyphosphoric acid and boric acid, such as sodium nitrate, potassium nitrate, ammonium nitrate, monosodium phosphate, disodium phosphate, monopotassium phosphate, dipotassium phosphate, monoammonium phosphate, diammonium phosphate, sodium sulfate, potassium sulfate, ammonium sulfate, sodium molybdate, potassium molybdate, ammonium molybdate, sodium acetate, potassium acetate, ammonium acetate, sodium tripolyphosphate, sodium hexametaphosphate, sodium pyrophosphate, soium borate and ammonium borate and those of the foregoing alkali agents are alkali metal hydroxides such as sodium hydroxide, potassium hydroxide and lithium hydroxide, and amines such as ammonia, monoethanol amine, diethanol amine and triethanol amine.
[0028] The foregoing mineral acids, organic acids, inorganic salts or alkali agents may be used alone or in combination.
SURFACTANTS
[0029] A surfactant can be added to the plate finisher of the present invention to improve the surface conditions or the like of the resulting coated film and to stably solubilize the solvent whose solubility in water at 20 °C is not more than 5 % by weight. Examples of the surfactants usable herein include anionic, nonionic, amphoteric and cationic surfactants.
[0030] Examples of such anionic surfactants include fatty acid salts, alkylbenzene sulfonic acid salts, straight chain alkylbenzene sulfonic acid salts, alkyl sulfonic acid salts, α -olefin sulfonic acid salts, alkyl phosphoric acid ester salts, dialkyl sulfo succinic acid ester salts, polyoxyethylene alkyl ether sulfonic acid salts, polyoxyethylene alkyl ether phophoric acid salts, alkylnaphthalene sulfonic acid salts, N-lauroyl sarcosine salts, sulfonic acid salts of condensates of naphthalene and formaldehyde, and diphenylether disulfonic acid salts.
[0031] Examples of the nonionic surfactants are polyoxyethylene alkyl ethers, polyoxyethylene alkyl phenol ethers, polyoxyethylene-polyoxypropylene brock copolymers, polyoxyethylene sorbitan fatty acid esters, polyoxyethylene glycerin fatty acid esters, polyethylene glycol fatty acid esters, polyoxyethylene fatty acid amines, fatty acid monoglycerides, sorbitan fatty acid esters, pentaerythritol fatty acid esters, sucrose fatty acid esters and amine oxides.
[0032] Examples of the amphoteric surfactants are alkylcarboxy betaines, alkylamino carboxylic acids and alkylimidazolines.
[0033] Examples of the cationic surfactants are tetraalkyl ammonium salts, trialkyl benzyl ammonium salts and alkyl imidazolinium salts. In addition, there may be mentioned fluorine atom containing surfactants and silicon atom containing surfactants.
[0035] The surfactants may be used alone or in combination. The amount thereof used is not limited to a specific range, but preferably it ranges from 0.01 to 10% by weight on the basis of the total weight of the plate finisher.
WETTING AGENTS, PRESERVATIVES AND OTHER ADDITIVES
[0036] In addition to the foregoing components, the plate finisher may further comprise a lower alcohol such as glycerin, ethylene glycol and triethylene glycol as a wetting agent. The amount of the wetting agent preferably ranges from 0.1 to 5.0 % by weight, more preferably 0.5 to 3.0 % by weight based on the total weight of the plate finisher. Moreover, the plate finisher may comprise other additives such as preservatives. Examples thereof are benzoic acid and derivatives thereof, phenol, formalin, sodium dehydroacetate and 3-isothiazolones These compounds may be used in an amount ranging from 0.005 to 2.0 % by weight of the plate finisher. Further, the plate finisher may contain other additives which are used in conventional plate finishers, for example, anti-foaming agents, chelating agents and coloring agents.
METHOD OF THE PREPARATION OF THE PLATE FINISHER
[0037] The plate finisher of the present invention can be prepared by dissolving with agitation the solvent, a water soluble resin, a surfactant, a pH adjusting agent, a wetting agent and a preservative in water or if necessary in hot water. Since the plate finisher of the present invention is a non-emulsion type gum solution, it is unnecessary to prepare a water phase and an oil phase and subsequently to emulsify the mixture with a homogenizer unlike an emulsion type gum solution. Thus, the plate finisher of the present invention can be prepared easily with an inexpensive equipment.
PRESENSITIZED PLATE
[0038] The plate finisher of this invention may be applied to various kinds of lithographic printing plates, in particular the plate finisher can suitably be applied to those obtained by imagewise exposing a presensitized plate (called "PS plate") comprising an aluminum substrate provided thereon with a light-sensitive layer and then developing the same. Examples of preferred such PS plates include those comprising an aluminum substrate provided thereon with a light-sensitive layer composed of a mixture of a diazo resin (a salt of a condensate of p-diazodiphenylamine and paraformaldehyde) and shellac as disclosed in British Patent No. 1,350,521; negative working PS plates such as those comprising an aluminum substrate provided thereon with a light-sensitive layer composed of a mixture of a diazo resin and a polymer mainly composed of repeating units derived from hydroxyethyl methyacrylate or hydroxyethyl acrylate as disclosed in British Patent Nos. 1,460,978 and 1,505,739; and positive working PS plates such as those comprising an aluminum substrate provided thereon with a light-sensitive layer composed of a mixture of o-quinonediazide light-sensitive substance and a novolak type phenol resin as disclosed in J.P. KOKAI No. Sho 50-125806. Preferred examples of such PS plates further include PS plates comprising an aluminum substrate provided thereon with a light-sensitive layer composed of a photocross-linkable photopolymer specifically described in U.S. Patent No. 3,860,426; PS plates comprising an aluminum plate provided thereon with a light-sensitive layer composed of a photopolymerizable photopolymer composition as disclosed in U.S. Patent Nos. 4,072,528 and 4,072,527; and PS plates comprising an aluminum plate provided thereon with a light-sensitive layer composed of a mixture of an azide and a water-soluble polymer as disclosed in British Patent Nos. 1,235, 281 and 1,495,861.
APPLICATION OF THE PLATE FINISHER
[0039] A method for using the plate finisher of the present invention will hereunder be explained specifically with reference to an example in which a PS plate is used.
[0040] First of all, a PS plate is imagewise exposed to light and then developed to give a lithographic printing plate.
[0041] A developer usable in the foregoing development is an alkaline solution whose principal solvent is water. The developer optionally comprises additives such as organic solvents, anionic surfactants and inorganic salts in addition to an alkaline agent.
[0042] Specific examples of the alkaline agents include inorganic alkaline agents such as sodium silicate, potassium silicate, potassium hydroxide, sodium hydroxide, lithium hydroxide, sodium tertiary phosphate, sodium bicarbonate, sodium carbonate, potassium carbonate and ammonium carbonate; and organic alkaline agents such as mono-, di- or tri-ethanolamine and propanolamine. The amount thereof used in the developer preferably ranges from 0.05 to 4 % by weight and more preferably 0.1 to 2 % by weight.
[0043] Examples of useful organic solvents are alcohols such as n-propyl alcohol and benzyl alcohol; and glycol ethers such as phenyl cellosolve. The organic solvents are added to the developer preferably in an amount ranging from 0.5 to 15 % by weight and more preferably 1 to 5 % by weight.
[0044] Examples of anionic surfactants include alkylsulfuric acid ester salts such as sodium laurylsulfate; alkylarylsulfonic acid salts such as sodium dodecylbenzenesulfonate; sulfonic acid salts of dibasic fatty acid esters such as sodium di-(2-ethylhexyl)sulfosuccinate; alkylnaphthalenesulfonic acid salts such as sodium n-butylnaphthalene-sulfonate; and polyoxyethylene alkyl(phenol) ether sulfates and in particular alkylnaphthalenesulfonic acid salts such as n-butylnaphthalenesulfonic acid salt are suitably used. The amount of the anionic surfactants in the developer preferably ranges from 0.1 to 5 % by weight and more preferably 0.5 to 1.5 % by weight.
[0045] Examples of inorganic salts are water-soluble alkali metal or alkaline earth metal salts of inorganic acids such as phosphoric acid, silicic acid, carbonic acid and sulfurous acid and, particularly preferred are alkali and alkaline earth metal salts of sulfurous acid. The amount of these inorganic salts in the developer in general ranges from 0.05 to 5 % by weight and preferably 0.1 to 1 % by weight.
[0046] It is also advantageous that the developer further comprises other additives such as antifoaming agents and wetting agents, if necessary.
[0047] The imagewise exposed PS plate can be developed with the foregoing developer in various known manners. Specific examples of methods for developing the imagewise exposed PS plate include a method comprising dipping the PS plate in a developer; a method comprising spraying a developer on the light-sensitive layer of the PS plate through a plurality of nozzles; a method comprising rubbing the light-sensitive layer of the PS plate with a sponge containing a developer; and a method comprising applying a developer to the surface of the light-sensitive layer of the PS plate with a roller.
[0048] The resulting lithographic printing plate thus developed is washed with water, the water is squeezed from the surface of the PS plate, then a proper amount of the plate finisher of the present invention is poured onto the plate surface. Then, the plate surface is rubbed with a sponge so that the plate finisher is uniformly distributed throughout the plate surface. As a result, non-image areas of the plate surface can be protected and hence the lithographic printing plate can stably stored.
[0049] The plate finisher can be applied to the plate surface in various manner, for example, by applying the plate finisher to the resulting lithographic printing plate after the development and water washing by use of an automatic gumming-up machine; supplying it to the printing plate immediately after the development without water washing; or applying it to the printing plate after water washing with a small amount of water or after rinsing with a rinse solution containing a surfactant by use of an automatic gumming-up machine.
[0050] The lithographic printing plate is in general washed with water, prior to the printing operation to remove the gum on the plate surface (so-called degumming step) and then printing is performed in a conventional manner. However, the plate finisher of the present invention makes it possible to directly perform the printing operation without carrying out such a degumming step. Moreover, the plate finisher of the present invention provides acceptable clear printed matters immediately after the initiation of the printing operation without providing a great number of unacceptable printed matters as usually observed when conventional gumming solution is used. Non-image areas treated by the plate finisher of the present invention are kept highly hydrophilic. Thus, the plate finisher of the present invention can provide good printed matters free of background contamination.
EXAMPLES
[0051] The present invention will hereunder be explained in more detail with reference to the following non-limitative working Examples and the effect practically achieved by the present invention will also be discussd in detail in comparison with Comparative Examples.
[0052] In the following Examples and Comparative Examples, the term "%" means "% by weight" unless otherwise specified.
Example 1
(a) Lithographic printing plate
[0053] An aluminum plate having a thickness of 0.24 mm was degreased by immersing it in 7% aqueous solution of tertiary sodium phosphate maintained at 60°C , washed with water and rubbed with a nylon brush with pouring an aqueous suspension of pumice stone to carry out graining. After washing with water, it was immersed in 5% aqueous solution of potassium silicate (molar ratio of SiO₂/K₂O = 2.0) maintained at 70 °C for 30 to 60 seconds. After sufficiently washing with water, the aluminum plate was dried.
[0054] The aluminum substrate thus treated was coated with a solution of a light-sensitive composition (hereunder referred to as "light-sensitive solution") comprising 2.0 parts by weight of 2-hydroxyethyl methacrylate copolymer (synthesized according to the method disclosed in Example 1 of British Patent No. 1,505,739), 0.12 part by weight of 2-methoxy-4-hydroxy-5-benzoylbenzenesulfonic acid salt of a condensate of p-diazodiphenylamine and paraformaldehyde, 0.03 part by weight of Oil Blue #603 (available from ORIENT CHEMICAL INDUSTRIES CO., LTD.), 15 parts by weight of 2-methoxyethanol, 10 parts by weight of methanol and 5.0 parts by weight of ethylene chloride to obtain a PS plate having a coated amount of the light-sensitive layer of 1.8 g/m² (weighed after drying).
(b) Plate finisher
Gum solution I
[0056] After the starches were dissolved in hot water at 80°C and cooled, the other components were added and dissolved with stirring to prepare a plate finisher.
Gum solution II
Gum solution III
[0059] In the same manner as in the preparation of Gum solution I, Solution A was prepared. Solution B was gradually added to Solution A with vigorous agitation to obtain an emulsion which was further emulsified with a homogenizer to prepare a plate finisher.
Gum solution IV
(c) Test
[0061] The PS plate prepared in step (a) was exposed to light through a negative transparency having halftone dot image. The exposed plate was processed in an automatic processor (Model 600 EII manufactured by FUJI PHOTO FILM CO., LTD.) having a developing zone provided with an aqueous developer comprising 3.0 parts by weight of sodium sulfite, 30.0 parts by weight of benzyl alcohol, 20.0 parts by weight of triethanolamine, 5.0 parts by weight of monoethanolamine, 10.0 parts by weight of sodium t-butylnaphthalenesulfonate and 1000 parts by weight of pure water, to develop the exposed plates, and a finishing zone provided with one part by volume of Gum solution I, II, III or IV prepared in step (b) and one part by volume of tap water, to apply each of the plate finishers to the developed plates immediately after the development without washing with water. Lithographic printing plates were thus prepared.
[0062] These printing plates were previously allowed to stand for 3 days in a thermo-humidistat at a temperature of 45 °C and a relative humidity (RH) of 85% or for 10 days at a room temperature. Each of the plates was set on a printing press Heidelberg SOR-M and printing operation was conducted without removing the gum in an usual manner using dampening water containing 10 % isopropyl alcohol. The number of spoiled printed matters before acceptable clear printed matters were obtained, background contamination and stability of the gum solutions were determined. The stability of the gum solutions was evaluated by storing the solutions under ambient conditions and observing the phase separation of the solutions. The results are shown in Table 1.
[0063] Comparative Example b used a conventional emulsion type gum solution III wherein a large amount of gum arabic was used. Comparative Example c used Gum solution IV wherein the amount of gum arabic was reduced and a large amount of a conventional water-soluble resin was used. Comparing with Comparative Example b, Comparative Example c was small in the number of spoiled printed matters but produced contamination in non-image areas during printing and was so unstable that the solution was separated into a water phase and an oil phase in a few days. Comparative Example a wherein the oil phase was removed was low in background contamination during printing and high in solution stability but produced many spoiled printed matters.
[0064] In contrast, Example 1 of the present invention wherein benzyl alcohol was added was smaller in the number of spoiled printed matters than the conventional emulsion type gum solution (Comparative Example b) and was low in background contamination during printing and high in solution stability. Further, the gum solution of Example 1 was prepared more easily using more inexpensive equipment than the emulsion type gum solutions of Comparative Examples b and c.
Example 2
(d) Lithographic printing plate
[0065] A light-sensitive solution was prepared by dissolving, in 40 parts by weight of methyl cellosolve, 1 part by weight of naphthoquinone-1,2-diazide-5-sulfonic acid ester of polyhydroxyphenyl obtained by polycondensing acetone and pyrogallol as disclosed in J.P. KOKOKU No. Sho 43-28403 and 2 parts by weight of novolak type cresol-formaldehyde resin.
[0066] A grained aluminum plate having a thickness of 0.2 mm was sufficiently washed and then dried. The foregoing light-sensitive solution was applied to the surface of the aluminum plate with a whirler and then dried to thus obtain a positive working PS plate having a light-sensitive layer in an amount of about 0.2 g/m².
(e) Test
[0067] The PS plate prepared in step (d) was exposed to light through a positive transparency having halftone dot iamage, developed with 3% aqueous solution of sodium silicate, washed with water and dried.
[0068] The exposed plate was processed in an automatic processor (Model 800 EB manufactured by FUJI PHOTO FILM CO., LTD.) having a developing zone provided with 3 % aqueous sodium silicate solution, to develop the exposed plates, and a finishing zone provided with one part by volume of Gum solution I, II, III or IV prepared in step (b) and one part by volume of tap water, to apply each of the plate finishers to the developed plates immediately after the development without washing with water. Lithographic printing plates were thus prepared.
[0069] These printing plates were previously allowed to stand for 3 days in a thermo-humidistat at a temperature of 45 °C and a relative humidity (RH) of 85% or for 10 days at a room temperature. Each of the plates was set on a printing press Heidelberg SOR-M and printing operation was conducted without removing the gum in an usual manner using dampening water containing 10 % isopropyl alcohol. The results are shown in Table 2.
Example 3, 4 and 5
[0071] The same procedures as in Examples 1 and 2 were repeated except that benzyl alcohol in Gum solution I was replaced by ethylene glycol monophenyl ether, propylpropylene diglycol or n-amyl alcohol. The results are shown in Table 3.
[0072] In all Examples, the number of spoiled printed matters was much smaller than Comparative Examples a and d and no background contamination was observed during printing.
[0073] The plate finisher of the present invention is excellent in the desensitizing ability and does not deteriorate the ink receptivity of image areas. Therefore, the lithographic printing plate to which the plate finisher of this invention is applied has good ink receptivity from the beginning of the printing operation. Moreover, the plate finisher of the invention is excellent in stability over time and can be prepared easily with an inexpensive equipment.
1. A gumming-up process which comprises applying to a lithographic printing plate consisting
of an oleophilic image area and a hydrophilic non-image area, a lithographic plate
finisher comprising, in uniform admixture, at least one water-soluble resin, an organic
solvent whose solubility in water at 20°C is not more than 5 % by weight, and water.
2. The process of claim 1 wherein the solvent whose solubility in water at 20°C is not
more than 5 % by weight is selected from the group consisting of benzyl alcohol, ethylene
glycol dibutyl ether, ethylene glycol benzyl ether, ethylene glycol monophenyl ether,
hexyl glycol, hexyl diglycol, propyl propylene diglycol, methyl phenyl carbitol, diethylene
glycol dibutyl ether, n-amyl alcohol, metyl amyl alcohol, isophorone, methyl cyclohexanone
and acetophenone.
3. The process of claim 1 wherein the solvent is benzyl alcohol.
4. The process of claim 1 wherein the amount of the solvent used is 0.1 to 10 % by weight
based on the total weight of the plate finisher.
5. The process of claim 1 wherein the amount of the solvent used is 0.5 to 5 % by weight
based on the total weight of the plate finisher.
6. The process of claim 1 wherein said water-soluble resin is selected from the group
consisting of starches derived from sweet potato, potato, tapioca, wheat, corn and
waxy corn; those derived from carrageenan, laminaran, sea weed mannan, funori (a glue
plant), Irish moss, agar and sodium alginate; mucilage derived from tororo-aoi mucin,
mannan, quince seed mucin, pectin, tragacanth gum, karaya gum, xanthine gum, guar
bean gum, locust bean gum, gum arabic, carob gum and benzoiun gum; dextran, glucan,
levan, succinoglucan and xanthane gum; glue, gelatin, casein and collagen; propylene
glycol alginate, viscose, methyl cellulose, ethyl cellulose, methyl ethyl cellulose,
hydroxyethyl cellulose, carboxymethyl cellulose, hydroxypropyl cellulose, hydroxypropyl
methyl cellulose and hydroxypropyl methyl cellulose phthalate; processed starches,
enzyme-modified dextrin, acid-treated starch, oxidized, gelatinized starch, esterified,
fatty acid starch, sulfuric acid starch, nitric acid starch, xanthogenic acid starch,
carbamic acid starch and succinic acid starch, etherified starch, crosslinked, and
starch graft copolymer; polyvinyl alcohol, modified polyvinyl alcohol, poly(meth)acrylic
acid derivatives; polyethylene glycol, polyethylene oxide, polyvinyl pyrrolidone,
polyvinyl pyrrolidone-vinyl acetate copolymer, carboxy vinylpolymer, styrene-maleic
acid copolymer and styrene-crotonic acid copolymer and is contained in an amount of
5 to 40 % based on the total weight of the plate finisher.
7. The process of claim 1 wherein said water-soluble resin comprises gum arabic in an
amount of 1 to 20 % by weight based on the total weight of the water-soluble resin.
8. The process of claim 1 wherein the plate finisher further comprises at least one wetting
agent selected from the group consisting of glycerin, ethylene glycol and triethylene
glycol in an amount ranging from 0.1 to 5.0 % by weight based on the total weight
of the plate finisher.
9. The process of claim 1 wherein the plate finisher further comprises at least one surfactant
selected from the group consisting of fatty acid salts, alkylbenzene sulfonic acid
salts, straight chain alkylbenzene sulfonic acid salts, alkyl sulfonic acid salts,
α -olefin sulfonic acid salts, alkyl phosphoric acid ester salts, dialkyl sulfo succinic
acid ester salts, polyoxyethylene alkyl ether sulfonic acid salts, polyoxyethylene
alkyl ether phophoric acid salts, alkylnaphthalene sulfonic acid salts, N-lauroyl
sarcosine salts, sulfonic acid salts of condensates of naphthalene and formaldehyde,
diphenylether disulfonic acid salts; polyoxyethylene alkyl ethers, polyoxyethylene
alkyl phenol ethers, polyoxyethylene-polyoxypropylene brock copolymers, polyoxyethylene
sorbitan fatty acid esters, polyoxyethylene glycerin fatty acid esters, polyethylene
glycol fatty acid esters, polyoxyethylene fatty acid amines, fatty acid monoglycerides,
sorbitan fatty acid esters, pentaerythritol fatty acid esters, sucrose fatty acid
esters, amine oxides; alkylcarboxy betaines, alkylamino carboxylic acids, alkylimidazolines;
tetraalkyl ammonium salts, trialkyl benzyl ammonium salts, alkyl imidazolinium salts;
fluorine atom containing surfactants and silicon atom containing surfactants in an
amount of 0.01 to 10% by weight based on the total weight of the plate finisher.
10. The process of claim 1 wherein the plate finisher further comprises at least one pH
adjusting agent and has pH of 2 to 6.
11. The process of claim 1 wherein the plate finisher further comprises at least one preservative
selected from the group consisting of benzoic acid, derivatives thereof, phenol, formalin,
sodium dehydroacetate and 3-isothiazolones in an amount ranging from 0.005 to 2.0
% by weight of the plate finisher.
12. The process of claim 1 wherein the plate finisher further comprises at least one selected
from the group consisting of anti-foaming agents, chelating agents and coloring agents.
13. The process of claim 1 wherein said lithographic printing plate is prepared by imagewise
exposing to light a presensitized plate comprising an aluminum support having a lithographically
suitable light-sensitive layer and then developing the imagewise exposed plate with
a developing solution to remove the non-image area of the light-sensitive layer.
14. The process of claim 13 wherein said light-sensitive layer comprises a light-sensitive
diazo resin and a polymeric binder.