Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
  • B41N1/00—Printing plates or foils; Materials therefor
  • B41N1/006—Printing plates or foils; Materials therefor made entirely of inorganic materials other than natural stone or metals, e.g. ceramics, carbide materials, ferroelectric materials

Definitions

• Lithographic printing plates have been widely used for many years.
• One of the basic concepts utilized in that technology is the establishment of differential wettability between areas on the planographic printing surface. This is most usually effected by providing a substrate having a hydrophilic or water we table surface and coating that surface with an imageable (usually visible light or radiation sensitive) and developable grease compatible (oleophilic) and hydrophobic layer. After imaging and developing of this layer/ the printing plate imagewise exposes hydrophilic and hydrophobic surfaces.
• the plate is first wet with water and then coated with grease or oil-based printing inks, only the hydrophobic areas of the image will hold the ink and provide a trans ⁇ ferred dark image when pressed against a receiving surface such as paper.
• This lithographic process has been able to provide planographic printing plates which are capable of producing as few as hundreds of copies or as many as several hundred thousand high quality copies.
• the desirability of being able to produce large numbers of copies from a single plate are quite apparent. Only a single imaging and developing procedure must be performed, and the printing press need not be shut down during operation in order to change plates.
• OMFI centered on the imageable and hydrophobic coating layer on the hydrophilic surface of the substrate. As it is usually the breakdown of this layer which causes failure of the printing plate, the logic of that direction of research is apparent.
• the substrate provided for the image ⁇ able layer is an aluminum sheet which has been prepared for coating by a variety of cleaning, mechanical, and chemical treatments.
• an aluminum surface is usually cleaned to remove oils and other contaminants. This cleaning is then followed by a mechanical or electro ⁇ chemical graining process, and finally an anodizing process.
• U.S. Patent No. 3,963,594 discloses the electrochemical etching of an aluminum substrate with an aqueous solution of hydrochloric acid and gluconic acid. This provides a uniformly coarse surface texture to the aluminum substrate.
• the process of that patent permits the use of lower current densities than were found to be necessary when using only hydrochloric acid in the bath.
• the treatment also coraplexed dissolved aluminum and other impurities which form in the etching bath. This extended the life of the bath. Desmutting treatments were also shown in combination with the electrochemical etching.
• 1,439,127 discloses an anodizing treatment for aluminum substrates in which the anodization is performed in an aqueous sulfuric acid bath at a temperature in excess of 70°C and with an anodizing current density of at least 50 amps/sq. ft. This treat- ment reduces the length of time in which the anodizing step is performed.
• Other etching solution compositions and electrical parameters are disclosed in U.S. Patents Nos. 4,072,589 and 4,052,275 and French Patent No. 2,322,015.
• an anodically oxidizing treatment is usually performed to render the aluminum surface both corrosion resistant and wear resistant. This is shown in British Patent 1,439,127 discussed above and in U.S. Patent No. 4,131,518.
• aluminum foil in the form of a continuous web particularly when the aluminum carries a polymeric coating on one side thereof, is anodized so that energy requirements are reduced and anodizing speeds are increased.
• U.S. Patent No. 3,181,461 discloses an anodizing process in which the sulfuric acid anodizing step is followed by treatment with an aqueous solution of sodium silicate. This treatment seals the pores of the anodic oxide surface and provides a hydrophilic, ink-repelling surface layer.
• German Patent (Offenlegungsschrift) 24 34 098 discusses firing a composition of aluminum phosphate and silicon carbide particles onto a metal surface for the purpose of increasing its wear resistance.
• this invention of German Patent 24 34 098 is not suitable for use on lithographic plates and is not coated on aluminum surfaces.
• a novel method for providing textured surfaces on lithographic printing plate substrates of aluminum was disclosed in U.S. Patent No. 3,210,184.
• a layer of boehmite (aluminum oxide monohydrate) was produced on the aluminum substrate by bathing the aluminum in hot water or steam in the presence of a weak organic base.
• Printing plates using the textured substrate were shown to provide increased numbers of copies under comparable conditions as compared to printing plates using mechanically roughened aluminum substrates.
• U.S. Patent Nos. 3,871,881 and 3,975,197 dis ⁇ close another method of enhancing the physical properties of aluminum surfaces.
• Various types of particulate material are bonded to the surface of the aluminum by an in situ formed binder of aluminum hydroxyoxide.
• the enhanced aluminum article is suggested for use as a susbstrate for printing plates.
• U.S. Patent No. 4,319,924 discloses an aqueous coating composition
• an aqueous coating composition comprising, in coating forming propor- tions: dissolved phosphate; dissolved dichromate; dissolved aluminum; and dispersed solid particulate material, preferably an aluminum-containing material.
• This composition is capable of being heat-cured at elevated temperatures into a water-insoluble material.
• the composition further comprises diethanolamine in an amount sufficient to reduce the temperature at which said composition can be cured into the water-insoluble material.
• a novel process for treating lithographic quality aluminum foil can provide a durable, long-running substrate for lithographic plate construc ⁇ tions.
• This process provides a novel substrate which can be resistant to the chemical action of the printing plate developers and press solvents.
• the novel substrate also enables the bonding of many photoreactive imaging layers to the treated aluminum substrate without the need for primers or other adhesion promoting agents.
• a process for firing a solution of monobasic phosphate, preferably monoaluminum phosphate on
• O PI an aluminum substrate or aluminized surface of a sub ⁇ strate.
• This process produces an aluminum sheet bearing a layer of glass or polymorphic forms of aluminum phosphate or mixtures of aluminum phosphates on at least one surface thereof.
• This coated layer has been found to provide an excellent surface for adhesion of organic materials.
• the aluminum phosphate layer provides excellent adhesion for diazonium resins and photopolymeric compositions used in the printing art and particularly in the planographic printing art.
• a process is also disclosed for firing a slurry of particles and a phosphate binder.
• the particles are preferably weakly basic or amphoteric non-metallic parti ⁇ cles and the composition is fired on an aluminum or aluminized substrate.
• This process produces an aluminum substrate or aluminized surface of a sheet bearing a textured layer of hard particles bonded together by a water resistant phase, or phases, of a dehydration products of monobasic phosphates such as those of aluminum and/or magnesium, alone or in combination with the products of their reaction with some or all of the particles, on at least one surface of the sheet.
• This textured layer has been found to provide an excellent surface for adhesion of organic materials.
• the phosphates strongly bind and adhere the particles into a layer having excellent adhesion for diazonium resins and photopolymeric composi ⁇ tions used in the printing art and particularly in the planographic printing art. This adhesion is enhanced by the surface texture and improved chemical stability imparted by the particles.
• the process of forming phosphate coatings on substrates according to the present invention provides a number of improvements over prior art processes for producing substrates for photoimaging elements, particularly in the continuous manufacture of substrates. Not only does the coated substrate of the present inven ⁇ tion have equivalent or improved properties as compared to materials of the prior art, but also it provides signifi ⁇ cant economic advantages in its manufacture. Apparatus used in the process consists of fewer separate items of equipment, thus requiring a lower capital investment than conventional forms of continuous substrate formation. The significant equipment eliminated includes the anodizing facility which is itself costly to operate because of high energy requirements and the need for safe effluent disposal.
• Such equipment is desirably eliminated from a substrate manufacturing line because of associated electro ⁇ chemical corrosion problems of other equipment on the same production line.
• the coating layer produced according to the present invention does not require etching or other texturizing. Such other texturizing may be optionally performed to provide additional characteristics to the surface. The elimination of such texturizing processes provides a further increment of cost reduction. The process can be readily performed in a continuous fashion and has been found to provide results substantially iden ⁇ tical to those of a batch process.
• a coating of a monobasic phosphate solution or a monobasic phosphate solution forming a slurry with metal oxide particles is applied to a clean aluminum or aluminized surface.
• This coating is fired at a tempera ⁇ ture of at least 450°F (230°C), preferably at least 500 or 550°F (260 or 290°C), to produce a ceramic coating of a phosphate glass.
• a textured coating is provided by the presence of the metal oxide particles and/or etching.
• This coating may comprise non-metallic and especially metal oxide particles embedded in a vitreous, water resistant phase or phases of a dehydration product of monobasic phosphates such as those of aluminum and/or magnesium, alone or in combination with the products of their reaction with some or all of the particles.
• monobasic phosphates which are acceptable include those of zinc, calcium, iron, and beryllium.
• the metal oxide is alumina, the bonding phase between the phosphate glass and the alumina is most likely aluminum orthophosphate.
• the firing should be performed for a long enough time at these temperatures to insure substantially complete dehydration of the coating. This may take place in as little time as three seconds at the described temperature depending upon the thickness of the coating and the temperature and other parameters of the firing process.
• the ceramic surface may be further treated as by etching to provide particularly desired textures and properties to the surface, but the surface resulting from the firing already is textured.
• This optional treating • is not critical or essential to the present invention and is most generally performed in conjunction with imaging systems (e.g., lithographic printing plates) which are optimized by a silicate treatment of the substrate or some other analogous layer.
• Etching for example, can be accom ⁇ plished by using known alkaline silicate solutions which will deposit a silicate coating at the same time. Where no silicating is required or where the subsequently applied light sensitive composition would not be compatible with a silicate surface, the etch may be performed in alkaline phosphate or aluminate solutions, for example.
• the aluminum or aluminized substrate may initially have a texturized surface so that etching of the ceramic coating will expose the texture through the ceramic coating. This is unnecessary, however, in the practice of the present invention because of the natural texture produced in the process.
• This natural texture which is a microscopic texturing visible by light scattering or under magnification, provides a physical structure to which subsequently applied light sensitive coating compositions may adhere.
• An optional post-firing etch may remove whatever amount of the dehydrated ceramic coating is necessary to provide the character required in the texture of the substrate. As little as five percent and as much as sixty percent by weight or more of the ceramic coating may be removed.
• the length of time of the etch is regulated by the temperature and pH of the etching environment. Higher temperatures and higher pH levels provide faster etches.
• the pH may be controlled by the addition of alkaline hydroxides such as sodium hydroxide.
• Replenishing solu ⁇ tions may be added during the continuous processing opera ⁇ tion to replace any material, such as the alkali component, which is depleted during the etch.
• the combined etch and silicating solutions are generally optimized to emphasize the silicating treatment, since the silicate etch has a wider performance latitude than phosphate or aluminate etching solutions.
• the silicates used for the combined etching and silicating baths are preferably at the high silica content end of the commer ⁇ cially available materials. Such materials as "Kasil #1" or “S-35" of the Philadelphia Quartz Co. or mixtures of "S-SS" with a fine silica sol (e.g., Sol #1115 of Nalco Chemical Co.) are particularly useful when diluted with water to give solutions having approximately one percent silica on a dry weight basis.
• the texturized substrates produced on the ceramic coated aluminum or aluminized substrate by the firing step may then be coated with a light sensitive composition either directly or with an intermediate sublayer.
• An oligomeric diazonium resin and/or an organic negative or positive acting photosensitive composition may be desirably applied to the textured surface.
• a broad range of photosensitive compositions having various different fields of utility are known to those of ordinary skill.
• the types of photosensitive coatings useful in the practice of the present invention are those which would ordinarily be considered for use in the printing plate art, and specifically, lithographic and relief compositions. These compositions would include both negative and positive acting lithographic composi ⁇ tions and negative acting relief compositions.
• Negative acting compositions ordinarily perform by having a photopolymerizable composition which becomes less soluble and/or more highly polymerized when struck by actinic radiation in an imagewise pattern. This is ordinarily accomplished by having a mixture of materials including such various ingredients as binders, polymeriz- able materials (monomers, oligomers and polymers), photo- initiator catalysts for the polyraerizable materials, sensitizers for the photocatalysts, and various other ingredients such as oleophilicity enhancers, pigments, surfactants, coating aids and other ingredients known in the art.
• Positive acting lithographic compositions ordinarily comprise a binder of thermoplastic or partially crosslinked compositions which contain a positive acting photosensitizer which, when struck by light, becomes more soluble in selected solvents than the non-light exposed sensitizer.
• the most common photosensitizers used in the art are o-quinone diazide compounds and polymers.
• Various binders such as acrylic resins, phenol formaldehyde resins (particularly novolaks), polyvinyl acetal resins, and cellu- losic esters are also generally known in the art for use with this type of photosensitizer. See, for example, U.S. Patent Nos. 4,193,797; 4,189,320; 4,169,732 and 4,247,616.
• Negative acting relief compositions work in similar fashion to negative acting lithographic systems, except that the layers are considerably thicker and that molds and embossing are often used to impress the surface structure when forming the relief image.
• the ceramic surface provided on the aluminum substrate is highly water receptive and has been shown to be at least as hydrophilic as anodized aluminum.
• the surface provides excellent adhesion for polymeric and oligomeric compositions.
• the surface has been found to provide particularly excellent adhesion for positive acting photosensitive compositions such as those containing diazo oxides and diazo sulfides, and provides good resistance to the developing solutions used which are generally highly alkaline.
• the thickness of the ceramic coating can readily be varied as desired, for example, between 0.2 and 15 micrometers.
• the coating layer is between 0.3 and 10 micrometers and more preferably is between 0.5 and 5 micrometers.
• the firing temperatures used in the practice of the present invention must be higher than 450 or 500°F (230 or 260°C) and preferably are at least 550°F (285°C). Temperatures higher than 700°F (370°C) do not offer any significant advantages and raise the energy requirements of the process and may distort or weaken the substrate. These temperatures refer to the surface temperature of the coating, measured by contacting the coating surface with the bare junction of a thermocouple. It will be under ⁇ stood that many different types of ovens having a variety of control characteristics may be used for achieving the required surface temperatures. The control temperature may in fact differ substantially from the surface temperature measured in the manner described above.
• the particulate matter added to the monobasic phosphate to form a slurry may have a considerable range and constitute substantially any non-metallic inorganic particle.
• non-metallic it is meant that the particle should not have such a high proportion of free metal (greater than 25% by weight on the surface) as would interfere with lithographic compositions.
• particles within a broad size range are useful, particles small enough to form colloidal dispersions, e.g., as small as average sizes of 5 x 10" ⁇ 3 micrometers and preferably no smaller than 1 x 10 ⁇ 3 micrometers are quite useful up to 45 micrometers.
• the preferred size range is between 10 ⁇ 2 and 45 micrometers, and the most preferred range is between 10 ⁇ 2 and 5 micrometers.
• highly reactive particles they will in effect dissolve away (in whole or in part) by reaction of material from the surface of the particle.
• surprisingly large particles can be used which would not interfere with the physical properties of the surface.
• Agglomerated particles having an effective large size which can be broken down during processing may also be used.
• the metal oxides may include alumina (in various phases such as alpha, beta, theta, and gamma alumina), chromia, titania, zirconia, zinc oxide, stannous oxide, stannic oxide, beryllia, boria, silica, magnesium oxide, etc. Certain oxides and even certain different phases of the oxides or mixtures thereof perform better than others. For example, the use of mixtures of alpha alumina and certain reactive transition aluminas such as the theta and gamma alumina provides a surface having improved properties over that obtained with particles of a single alumina phase.
• the presence of the alpha phase in the slurry provides a ceramic coating with increased wear resistance and the presence of the other phases, or other metal oxide particles, tends to provide a more finely textured surface than alpha alumina by itself.
• 'reactive' it is meant that the oxide reacts with monobasic phosphate during firing conditions.
• OMPI Particulate materials which react with the acid or monobasic phosphate give more alkali-resistant binder compositions. When such materials are added in excess of the amount that will react fully with phosphate, they may additionally contribute to the surface texture of the fired coating. If they are in a form that reacts slowly or not at all at room temperature, they may contribute to the consistency or viscosity of the slurry, giving a formulation that may be particularly well-adapted for particular coating methods. Furthermore, some of these materials detract from or add to the hydrophilicity of the phosphate coating in a controlled way.
• a reactive inorganic material most desirably present is a magnesium compound.
• Magnesium carbonate, magnesium oxide, magnesium hydroxide, and monomagnesium phosphate have been used, and the characteristic, desirable, contribution to alkali resistance was obtained in each case.
• Zinc oxide, zinc carbonate or zinc phosphate could be substituted for the magnesium compound, though slightly poorer alkali resistance was obtained with the zinc compounds than with the magnesium compounds.
• magnesia i.e., magnesium oxide or magnesium hydroxide
• the amount of magnesia, i.e., magnesium oxide or magnesium hydroxide, generally added is not enough to yield a fully tribasic (dehydrated) phosphate composition upon firing, so additions of other materials supplying polyvalent cations will in general give further alkali resistance.
• Hydrated or transition aluminas, sols of many metal oxides, or blends of these materials may be added, generally together with magnesia and generally in such proportions as to optimize the coating as noted above.
• the resulting fired slurries tolerated moderate levels of alkali metal oxides, such that commercial or technical grades of materials are generally acceptable; however, compounds containing major amounts of alkali metal cations are not recommended.
• silica sol When silica sol is added, compensating extra metallic oxide should also be added to optimize alkali resistance.
• particles of hard, wear- resistant materials may be added with good effect. In general these are expected to react only superficially with the phosphate bonding material, and not to contribute substantially to insolubilization.
• Graded alpha alumina of the type of *381200 Alundura supplied by the Norton Co. of Troy, N.Y.
• I was substituted for or blended with alumina in several proportions without loss of properties.
• Graded fine sands of other hard materials such as quartz, amorphous silica, cerium oxide, zirconia, zircon, spinel, aluminum silicate ( ullite) , and even hydrophobic particles such as silicon carbide, among many others, would be expected to function satisfactorily, though perhaps (as compared to alumina) to have less attractive cost or availability as closely-sized powders. It is preferred to use hydrophilic particles in the practice of the present invention, and especially metal oxides.
• the present process is highly flexible and can be readily altered to provide substrates which fit changed requirements. It should be noted that one can practice the present invention by forming monoaluminum phosphate or other acid phosphates ⁇ n situ during the firing step. This can be accomplished, for example, by coating a slurry of phosphoric acid and a stoichiometric excess of reactive alumina onto the aluminum or aluminized surface to be fired. Aluminum phosphate is generated during the initial firing period, and with a stoichiometric excess of alumina present, reactive alumina particulate material will remain in the reactive composition during the continued firing.
• monoaluminum phos ⁇ phate or other aluminum phosphates or mixed phosphates of aluminum and other metals i ⁇ _ situ is contemplated as being within the scope of practicing the present invention.
• monoaluminum phosphate __ situ or mixed phosphates of aluminum and other metals __ situ by reacting stoichiometrically equivalent amounts of reactive alumina, i.e., aluminum oxide or aluminum hydroxide, with either phosphoric acid or an alkaline earth acid phosphate such as monomagnesium phosphate solution.
• reactive alumina i.e., aluminum oxide or aluminum hydroxide
• alkaline earth acid phosphates may be created in solution by mixing an appropriate alkaline earth tribasic phosphate with phosphoric acid. For example,
• addition of calcium- containing inorganic compounds to the slurry reduces the necessity for close monitoring of the firing temperature, by providing a mixture that is effectively dehydrated at somewhat lower temperatures or shorter times.
• the calcium addition is preferably in the form of calcium hydroxide, calcium carbonate, calcium oxide, calcium phosphate, or mixtures thereof.
• the magnesium-containing compound as a soluble phosphate and the aluminum-containing compound in an ultrafine and/or dissolved condition.
• addition of calcium- containing inorganic compounds to the slurry contributes to a coating composition that may be fired at a lower temperature or in less time, while retaining lithographic quality at greater coating thicknesses than previously possible.
• the aluminum-containing compound may be a fumed alumina, e.g. that produced by flame hydrolysis of anhydrous aluminum chloride, having mean ultimate particle diameter less than 20 nanometers.
• a fumed alumina e.g. that produced by flame hydrolysis of anhydrous aluminum chloride, having mean ultimate particle diameter less than 20 nanometers.
• phosphate and silicate tends to weaken the coating mechanically, giving less abrasion resistance of the type described by ANSI-ASTM tests C501-66 and D1044-76, or a test combining some of the features of each of the two standard tests.
• the slurries or solutions generally contain between 85 and 95% (by volume) of material that is volatile upon firing, the actual amount being that required to yield a satisfactory coating weight and satisfactory coatability with the chosen coating tech ⁇ nique.
• the volatile material is generally water, although water-miscible volatile liquids such as alcohols may be added in substantial part.
• the volume of volatile material stated above includes both the volatile material added as solvent or diluent, and that generated by reac- tions such as pyrolysis of organics or acid-base metathesis.
• the second largest constituent of the slurries or solutions, which constituent may or may not be present, is a form of hard particles, such as the alpha aluminas mentioned previously. These may comprise between zero and 65% of the volume of the non-volatile portion.
• the size, shape, volume and type of hard particles is varied as needed to accommodate the intended specific use of the ceramic-coated material.
• a coating containing more than 65% hard particles by volume will be too lean in binder material with the result that the hard particles will not be securely bonded, and the voids between them may tend to trap ink in areas required to remain free of ink when the coating is used as a lithographic substrate.
• a fired film containing 45-60% by volume hard particles is dominated by relatively coarse features.
• This type of surface is desirable for use with some image coatings.
• Fired films containing less than 50% by volume hard particles may have their surfaces increasingly dominated by ultrafine features, because the relative volume of hard particles declines, while the relative volume of ultrafine particles increases.
• the ultrafine features are more desirable for use with some image coatings.
• Sedimentation and agglomera ⁇ tion of hard particles may be a source of coating problems, Where a formulation is required wherein the main charac ⁇ teristic is ease of coating with simple apparatus, the reduction of the volume of, or the complete elimination of, the coarser particles may be preferable.
• the hard particles considered for use in this invention react so slowly with phosphate solutions that they are presumed to undergo negligible reaction during firing.
• the remaining constituent of the slurry formula- tion is a matrix or bonding constituent.
• phosphoric acid alone may be coated and fired; how ⁇ ever, useful properties are enhanced by using acid phos ⁇ phates, such as monoaluminum phosphate, and/or reactive particles, such as alumina. Greater chemical resistance than can be obtained with a coating derived from phosphoric acid employed by itself is essential or at least preferred.
• CMPI greater chemical resistance reactive particles which yield metal ions should be added to the phosphate solution in quantities sufficient that an orthophosphate or mixture of orthophosphates is created upon firing.
• the reactive particles are of a chemical species which yield calcium ions
• a quantity ranging from about 0 to about 20% of the amount that would combine with the available phosphate ions to give calcium ortho ⁇ phosphate is used.
• Calcium additions in excess of 20% result in coagulation of the slurry, and are likely to result in a decline in acid resistance of the final article.
• Quantities in the range of about 4 to about 7% give the maximum reduction of firing temperature with no noticeable degradation of acid resistance or slurry viscosity.
• a solution of monocalcium phosphate, rather than particles which yield calcium ions, may be used to provide the calcium content.
• the reactive particles are of a chemical species which yield magnesium ions
• a quantity ranging from about 0 to about 35% of the amount that would combine with the available phosphate to give magnesium orthophosphate is used. Quantities in the range of about 10 to about 20% are preferred.
• magnesium-containing particles are added at a level greater than 35% to monoaluminum phosphate, the resulting coating will flake away from the aluminum substrate upon cooling down from the firing temperature. Amounts of magnesium at lower than the 10% level are found to provide a less than optimum contribution to alkali resistance.
• magnesium phosphate solution containing 5.3% MgO and 32.6% 2O5 by weight, may be used to provide magnesium ions since the amounts of magnesium and phosphate provided by this solution, with no other phosphate addition, give a magnesium ion addition of 19.1% of the amount required to yield magnesium orthophosphate.
• Reactive particles yielding aluminum ions may be added in quantities ranging from about 0 to about 200% of the amount which, in combination with all other metal and phosphate ions present or liberated during firing, would give stoichiometric orthophosphate.
• the preferred range is 100-150%.
• the preferred amount of aluminum ion-containing material to be added would be in the range of 80-130% of the amount that would yield aluminum orthophosphate.
• Dispersants such as gluconic acid may also be added to the slurry.
• Alkaline dispersants such as sodium tripolyphosphates are not preferred even though they do not destroy the function of the present invention.
• Pretreatment of the coarsest particles as with colloidal silica, may make the resulting slurries more stable against sedimentation.
• Lithographically useful compositions may, of course, be coated on the ceramic surface.
• Such composi ⁇ tions would comprise 1) oligomeric diazonium resins, 2) positive acting diazo oxides or esters, 3) photopoly- merizable organic compositions (particularly such as ethylenically unsaturated materials in the presence of free radical photoinitiators) , 4) oligomeric diazonium resin undercoats with photopolymerizable organic composi ⁇ tion overcoats, and 5) any other various well known litho- graphically useful photosensitive compositions.
• Example 1 A precleaned aluminum foil was coated with a solution of 50 weight percent monoaluminum phosphate in water and dried below 100°C to a coating thickness of about 3 micrometers. The surface temperature of the coating was raised to 550°F (260°C) in ninety seconds in an oven and removed after thirty seconds at that tempera ⁇ ture.
• a positive acting photosensitive composition as described in Example 3 of U.S. Patent No. 4,247,616 was coated onto the treated surface after rinsing and drying. The composition adhered to the substrate and developed off cleanly after exposure.
• Example 2 A precleaned aluminum foil was coated with a composition comprising, by weight, 12% transition alumina (nominally 0.5 micrometers diameter of gamma or theta phase alumina), 15% monoaluminum phosphate, .0.75% magnesium oxide (particle size less than 200 mesh), and 72.25% water. The coating was dried to a thickness of about 3 micrometers. The coated foil was placed in an oven and the surface temperature of the coating was raised to 550°F (260°C) in thirty seconds. Dwell time in the oven was one and one half minutes. The coated foil was cooled, rinsed, and dried, then rolled up.
• the foil was subsequently unrolled and coated wijh the positive acting photosensitive composition of the previous example.
• the photosensitive layer adhered well to the substrate and developed off cleanly with no undesir ⁇ able undercutting of the half tone image.
• the background areas were less readily attacked by alkaline developer than was the substrate of Example 1.
• Example 3 The procedure of Example 2 was repeated except that 1% zinc oxide was used in place of the magnesium oxide and correspondingly less water was used.
• the coated aluminum was found to be somewhat less resistant to developer chemicals than the sheet of Example 2, but still provided excellent adherence to the photosensitive layer and provided a useful printing plate surface.
• Example 4 The procedure of Example 2 was repeated, using the same coating composition, but with firing effected at 600°F (310°C). No differences were observed between the mechanical or chemical properties of the materials. Both were presumed to be fully dehydrated.
• Example 2 The procedure of Example 2 was repeated using a coating composition having 8 percent reactive (e.g. , theta transition alumina) alumina (nominally 0.5 microns diameter), 0.5 percent dead-burned magnesia (particle size less than 200 mesh), and 4.0 percent alpha alumina
• aqueous gluconic acid A water and monoaluminum phosphate solution was used to provide the above weight percentages of metal oxides and 15 percent by weight of monoaluminum phosphate and 66 percent water.
• the alpha alumina content conferred additional wear resistance and a higher arithmetic average roughness to the fired coating. These additional properties are advantageous in many image coating systems.
• Example 6 The fired substrate of Example 2 was immersed for 2-1/2 minutes in a solution containing 5% by weight Phila. Quartz Co. "Star” brand sodium silicate solution at 95°C, then rinsed in a deionized water spray and dried. It was coated with a negative oligomeric diazonium resin and an 8 micron dried thickness coating of the negative photopolymeric composition of Example 2 of U.S. Serial No. 103,712, filed December 14, 1979.
• the image develoepd cleanly upon conventional exposure and development. It gave many thousands of good inked impressions during an accelerated press wear test, at least equalling the wear performance of the same image material on conventional grained and anodized aluminum.
• Example 7 A slurry was prepared consisting of 19.1% (wt. )
• Norton Co. "#381200 Alundum” brand alpha alumina (prior to addition it had been cleaned by firing overnight in air at 600°C); 2.4% Alcoa "Hydral 710" alumina trihydrate; 0.75% Condea Cheraie "Dispural 10/2” alumina monohydrate; 0.36% Martin Marietta “MagChem 10" magnesia, and 14.4% 50% monoaluminum phosphate solution, plus some surface-active materials as follows. The dry powders were milled together as a 30% solids slurry.
• alpha alumina was milled alone in a solution containing all the water of the 30% slurry and 2% of the weight of alumina as Nalco "Nalcoag 1115" colloidal silica, for one hour. Then enough 50% gluconic acid was added to make the aqueous
• Example 8 A slurry was prepared, coated and fired similarly to that of Example 7 except that the proportions were grade 1200 alpha alumina, 17.8%; Alcoa "Hydral 710", 3.2%; Condea "Dispural 10/2" 0.7%; MgO, 0.38%; the milling times were 30 min. for alpha alumina in silica sol, and 4 hours for all solids at 40% solids; the phosphate addition was 15.4% 50% monoaluminum phosphate solution.
• Example 9 The slurry of Example 8 was roll coated onto Bethlehem Steel Co. "Duraskin” sheet, which is steel sheet plated with a predominately aluminum, aluminum-zinc- silicon alloy, and rerolled to .010 in. thickness.
• the "Duraskin” sheet was precleaned using the same "Scotch-brite” brushing technique described in Example 8.
• the fired material functioned very well as the substrate for either negative- or positive-working, long-wear life, lithographic plates; no significant differences being ob ⁇ served between it and the lithoplates of Example 8 in its image contrast or resolution, or its wear characteristics.
• Example 10 A slurry was prepared consisting of 19.05%
• Example 7 0.02 micrometers; 32.9% deionized water; and 47.4% of the Mobil Chemical Co. 50% monoaluminum phosphate solution.
• the silica and colloidal alumina were first mixed together in the water, then the phosphate solution was added. This slurry was coated onto the substrate of Example 7 and fired as in the same Example. It was then immersed 25 seconds in an 80°C solution containing 4.8 wt. % "Kasil No. 1" potassium silicate solution available from the Philadelphia Quartz Co. , rinsed in deionized water and air dried. The resulting sheet was primed with a negative- working diazo compound and overcoated with a negative- working photopolymer of a type well-known in the art.
• Example 11 A slurry was prepared consisting of 15.08% (wt.) Norton Co. "#381200 Alundum” brand alpha alumina (prior to addition it has been cleaned by firing overnight in air at 600°C), 0.45% (wt.) "Nalcoag 1115" 15% aqueous colloidal silica suspension, 0.45% (wt.) 50% aqueous gluconic acid solution, 62.12% (wt.) deionized water, 2.72% (wt.
• the resulting lithographic plate When cooled and coated with a posi ⁇ tive working composition of the diazo oxide-phenolic resin type well known in the art, the resulting lithographic plate was capable of state-of-the-art performance, with regard to resolution, ink/water balance, and wear life, as determined by accelerated wear tests.
• a slurry was prepared consisting of 18.64% (wt.)maschineacher “WSK” F1200 alumina (prior to addition it had been cleaned by calcining at 600°C) 0.56% (wt. ) "Nalcoag 1115" 15% aqueous colloidal silica suspension, 0.44% (wt. ) 50% aqueous gluconic acid solution, 58.64% (wt.) deionized water, 4.21% (wt. ) "Aluminum Oxide C", manufactured by Degussa Pigments Division of Frankfurt, Germany, 17.00% (wt.
• Example 13 A precleaned, ungrained aluminum foil was coated with a solution of 25 weight percent monoaluminum phosphate in water and dried above 100°C to a coating thickness of about 3 micrometers. The surface temperature of the coating was raised to 550°F (260°C) in ninety seconds in an oven and removed after thirty seconds at that temperature.
• a positive acting photosensitive composition as described in Example 3 of U.S. Patent 4,247,616 was coated onto the treated surface after rinsing and drying. The composition adhered well to the substrate and developed off cleanly after exposure.
• Example 14 A precleaned, ungrained aluminum foil was coated with a composition comprising, by weight, 12% alumina (nominally 0.5 micrometers diameter), 15% monoaluminum phosphate, 0.75% magnesium oxide (particle size less than 200 mesh), and 72.25% water. The coating was dried to a thickness of about 3 micrometers.
• the coated film was placed in an oven and the surface temperature of the coating was raised to 550°F (260°C) in thirty seconds. Dwell time in the oven was one and one half minutes. The coated film was cooled, rinsed, and dried, then rolled up.
• Example 15 The procedure of Example 14 was repeated except that 1% zinc oxide was used in place of the magnesium oxide and correspondingly less water was used.
• the coated aluminum was found to be somewhat less resistant to developer chemicals than the sheet of Example 14, but still provided excellent adherence to the photosensitive layer and provided a useful printing plate surface.
• "Kasil #1" brand potassium silicate solution Philadelphia Quartz Co.
• the silicate treated foil was rinsed in a spray of deionized water for 30 seconds, dried, and coated with a 12 micron negative acting photo ⁇ polymeric composition having acrylate monomers and a photosensitizer.
• a 12 micron negative acting photo ⁇ polymeric composition having acrylate monomers and a photosensitizer.
• the aluminum phosphate coated plate gave at least as many good impressions before showing wear, as the factory-made anodized plate.
• Example 18 A grained aluminum foil prepared, phosphate coated and fired as in Example 16, and similarly etched except in a pH 10.4 solution of sodium pyrophosphate at 70°C, was coated with a positive-working photopolymeric composition, and tested similarly against a factory-made plate. It gave several times as many copies before showing wear as the Tartan 25 plate, which is brush grained similarly to the experimental plate but is not hard coated or anodized.
• Example 19 A grained aluminum foil prepared, phosphate coated and fired as in Example 16, was etched as above except in a pH 10.4 solution of "Nalco 680" sodium aluminate, made by the Nalco Chemical Co., and tested similarly. It gave several times as many copies before showing wear as the factory-made plate.

Landscapes

• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Ceramic Engineering (AREA)
• Inorganic Chemistry (AREA)
• Printing Plates And Materials Therefor (AREA)

Applications Claiming Priority (4)

Publications (3)

Family

ID=26971370

Family Applications (1)

Country Status (5)

Families Citing this family (5)

Citations (2)

Family Cites Families (6)

• 1982
  • 1982-09-08 BR BR8207853A patent/BR8207853A/pt not_active IP Right Cessation
  • 1982-09-08 AU AU89599/82A patent/AU553537B2/en not_active Ceased
  • 1982-09-08 WO PCT/US1982/001209 patent/WO1983000844A1/en active IP Right Grant
  • 1982-09-08 EP EP82902955A patent/EP0087469B1/de not_active Expired
  • 1982-09-08 DE DE8282902955T patent/DE3268962D1/de not_active Expired

Patent Citations (2)

Non-Patent Citations (2)

Also Published As

Similar Documents

Legal Events