US3415187A - Lithographic plate and method for manufacturing same - Google Patents
Lithographic plate and method for manufacturing same Download PDFInfo
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- US3415187A US3415187A US623555A US62355567A US3415187A US 3415187 A US3415187 A US 3415187A US 623555 A US623555 A US 623555A US 62355567 A US62355567 A US 62355567A US 3415187 A US3415187 A US 3415187A
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- coating
- lithographic
- adhesive
- base
- drying
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- 238000000034 method Methods 0.000 title description 25
- 238000004519 manufacturing process Methods 0.000 title description 8
- 238000000576 coating method Methods 0.000 description 63
- 239000011248 coating agent Substances 0.000 description 60
- 239000002585 base Substances 0.000 description 53
- 239000000853 adhesive Substances 0.000 description 42
- 230000001070 adhesive effect Effects 0.000 description 42
- 239000000123 paper Substances 0.000 description 35
- 238000001035 drying Methods 0.000 description 30
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 22
- 230000005012 migration Effects 0.000 description 21
- 238000013508 migration Methods 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000007787 solid Substances 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- 239000008199 coating composition Substances 0.000 description 11
- 239000011787 zinc oxide Substances 0.000 description 11
- 238000001704 evaporation Methods 0.000 description 10
- 239000000945 filler Substances 0.000 description 10
- 230000008569 process Effects 0.000 description 10
- 230000008020 evaporation Effects 0.000 description 9
- 229920002125 Sokalan® Polymers 0.000 description 8
- 239000004584 polyacrylic acid Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 230000033458 reproduction Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 238000009825 accumulation Methods 0.000 description 6
- 230000001680 brushing effect Effects 0.000 description 6
- 239000004927 clay Substances 0.000 description 6
- 238000003384 imaging method Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 229920000877 Melamine resin Polymers 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- -1 or the like Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 238000003490 calendering Methods 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 238000010981 drying operation Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 238000004873 anchoring Methods 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000008098 formaldehyde solution Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 2
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 239000004246 zinc acetate Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- MJWPFSQVORELDX-UHFFFAOYSA-K aluminium formate Chemical compound [Al+3].[O-]C=O.[O-]C=O.[O-]C=O MJWPFSQVORELDX-UHFFFAOYSA-K 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 1
- 230000005660 hydrophilic surface Effects 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 235000019988 mead Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000011120 smear test Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002982 water resistant material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
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
- B41N3/00—Preparing for use and conserving printing surfaces
- B41N3/03—Chemical or electrical pretreatment
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof
Definitions
- the present invention relates to the preparation of new and improved surfaces having lithographic properties. More particularly, it rel-ates to lithographic plates of improved characteristics and to methods of producing same by reducing mi ration of adhesives used therein to the exposed surface of the coating before and during drying.
- Prior art Lithographic surfaces have previously been prepared by applying to suitable carriers, such as paper, coating compositions comprising casein and ester gum to function as a Water receptive hydrophilic colloid, inert fillers such as clay, and formaldehyde.
- suitable carriers such as paper
- coating compositions comprising casein and ester gum to function as a Water receptive hydrophilic colloid, inert fillers such as clay, and formaldehyde.
- Such coatings were applied in one or more layers depending upon the number of copies to be made from the lithographic plate. Fol-lowing application and drying of the coating, it was necessary for the outer or exposed surface of the coating to be then subjected to a subsequent treatment in order to render the surface suitable for the production of uniform reproductions.
- Such subsequent treatment usually consisted of brushing or abrading the surface to remove excessive adhesive, or the insolubilization thereof by application of a wash coat comprising a solution of a polyvalent metal, such as a solution of aluminum chloride, zinc chloride, aluminum form-ate, or the like.
- a wash coat comprising a solution of a polyvalent metal, such as a solution of aluminum chloride, zinc chloride, aluminum form-ate, or the like.
- the base of the plate is an inexpensive paper, such as kraft
- the paper to swell and change dimensions as the water application of water to the plate has a tendency to cause penetrates the surface coating and reaches the paper base.
- Such changes cause distortion: of the image, imperfect registration and deterioration of the paper base.
- the surface of the plate may not be completely wetted by the solution because of the fact that it has been withdrawn from the surface into the plate.
- the surface of the plate may not repel the printing ink and hence areas of the surface which should be perfectly blank will show backgrdimd discoloration or become darkened or toned. This iiiomplete wetting of the surface of the plate may also occpr during printing.
- the adhesive employed for holding the coating onto the base be of such character that it satisfactorily bonds the coating layer and at the same time is subject to a minimum tendency to migrate to the outer or exposed surface of the coating, or into the base stock during the drying operation.
- Migration of the adhesive to the outer surface of the lithographic plate causes an undue accumulation of adhesive on the surface and seals the latter, thereby preventing the imaging material from penetrating the surface and firmly anchoring thereto.
- migration of adhesive into the base stock produces a surface layer relatively low in adhesive content and not sufficiently bonded to anchor the image.
- an object of the present invention is to provide means for obviating the difliculties previously inherent in paper base lithographic plates.
- Another object is to produce and to provide a method for producing a new and improved lithographic surface using high speed coating techniques.
- Still another object is to produce and to provide a method for producing a lithographic plate of the type described which requires consider-ably fewer operational steps in its manufacture and which during use is capable of holding an ink-receptive image having the properties of immediate reproduction of copy of good quality.
- Another object is to provide a method of controlling adhesive migration during application of lithographic coatings to a paper base.
- Yet another object is to produce and to provide a method for producing a paper base lithographic plate of the character described which is useful either as a direct image master or as an indirect image master where the existing image produced elsewhere is transferred to a coating surface produced in accordance with the invention.
- a further object is to produce an improved lithographic plate of the type described which is easy and economical to manufacture and use, is characterized by excellent stability, is capable of holding tenaciously an inkreceptive image having the properties of immediate reproduction of copy of good quality and which continues to produce such copies for a considerable period of time.
- the process of the present invention relates to a method for effecting the drying of lithographic plates, and particularly paper base lithographic plates, in a manner so as to substantially reduce migration of the adhesive content to the exposed surface of the coating during said drying operation. More specifically, it relates to an improvement of the product and process of Beatty US. Patent 2,760,431, referred to above. Applicants have discovered that by effecting drying of the Beatty coating in the manner discovered by them and specifically described below, consistent and uniform printing results can be obtained without resorting to the added step of brushing or abrading or washing with a solution of a polyvalent metal salt, as required when plates are produced as described by Beatty.
- the Beatty product is obtained by coating a base with a composition containing an inert filler, polyacrylic acid and a metal base selected from the group consisting of the oxides and hydroxides of zinc, magnesium, calcium, barium and lead, and mixtures thereof, and present in the ratio of 1 part by weight of metal base to 2-20 parts by weight of filler and 1 part by weight of polyacrylic acid to 2-10 parts by weight filler plus metal base and with ammonium ions present in amounts in excess of that necessary to maintain the solubility of the polyacrylic acid in the presence of the metal base.
- a composition containing an inert filler, polyacrylic acid and a metal base selected from the group consisting of the oxides and hydroxides of zinc, magnesium, calcium, barium and lead, and mixtures thereof, and present in the ratio of 1 part by weight of metal base to 2-20 parts by weight of filler and 1 part by weight of polyacrylic acid to 2-10 parts by weight filler plus metal base and with ammonium ions present in amounts in excess of that necessary
- the resulting composition in the form of 40-60% solids content with water was coated onto a suitable base in an amount sufficient to give a coating weight of 6-30 pounds per 3300 square feet surface and then dried by passage through an air drying oven heated to a temperature in excess of 250 F.
- the lithographic plates thus produced required treatment by brushing or abrasion or washing with a solution of a polyvalent metal salt before consistent lithographic printing results were obtainable.
- the subsequent brushing, abrading or washing step is not required for satisfactory lithographic printing results if the lithographic coating is subjected to a drying operation whereby the migration of adhesive to the outer or exposed coating surface is reduced to a minimum. They have also discovered that this type of drying can be accomplished in different manners so long as the solvent for the adhesive (water plus ammonia) is evaporated substantially within the coating and principally at the coating base sheet interface rather than at the exposed surface of the coating. In other words, evaporation of the liquid solvent must be effected substantially in a region within said coating away from the exposed coating surface.
- evaporation of solvent in the coating composition is most satisfactorily effected by use of infra-red rays or by application of heat to the uncoated side of the coated base, such as by contacting the uncoated surface of the base with a dryer drum. Yankee dryer or impinging hot air. Since heat is generated throughout the coated paper by absorption of the infra-red rays, these rays may be applied from either the uncoated or the coated side of the base. In any event, it is highly important to the success of the present invention that heat not be applied to the outer or exposed coating surface until after the coating has dried to a substantially non-tacky state, whereby the liquid portion of the coating is immobilized.
- the liquid solvent and adhesive When heat is applied directly to the exposed surface, the liquid solvent and adhesive first migrate to the surface where evaporation of the solvent takes place and thereby permitting an 'accumulation of adhesive at the lithographic surface.
- evaporation takes place substantially Within the coating and at the coatingbase interface, thus reducing accumulation of adhesive at the lithographic surface.
- the migration of adhesive to the lithographic surface is also affected by such factors as the character of the adhesive, the quantity thereof used in the coating, the coat weight, the solids content of the coating, as well as the method of drying. For example, migration of adhesive is reduced by using a lower coat weight and a higher solids content than customarily employed, as well as by effecting the drying of the wet coating by the method of this invention. While each of these factors is important, the most satisfactory general results are obtained by the use of a combination of these factors.
- the coat weight used should be sufficient to form a continuous lithographic surface but should not be so heavy as to cause cracking of the coating. -In addition to providing poor coverage over the base coat, insufficient coat weight results in short copy life. Excess coat weights, in addition to causing increased adhesive'migration, cause surface cracking which results in reproduction of the cracks on the copy and also in short copy life.
- the proper coat weight employed will depend to some extent upon the composition of the paper base which, in turn, depends upon the desired copy life. For example, tests have shown that a paper raw stock which has been tub sized and then given two base coats should preferably use a coat weight ranging from one to five pounds per 3300 square feet. Generally, a four pound coat has given optimum results, other critical factors being the same. However, acceptable levels of lithographic surfaces have been obtained outside this range.
- the inert filler can include such materials as chalk, talc, satin white, silica, and the like.
- the various constituents of the coating should preferably be present within certain specified ranges.
- the zinc oxide and adhesive should preferably be present in the ratio of 1 part adhesive to 1-4 parts of zinc oxide.
- the zinc oxide and inert filler are preferably present in the ratio of part zinc oxide to 2 parts inert filler.
- the ratio of adhesive to zinc oxide plus inert filler is preferably 1 to 2 parts polyacrylic acid to parts of zinc oxide plus inert filler.
- Suitable supports for the lithographic surface can include paper, fiberboard, textile fabrics, plastic sheet stock or metal strips, preferably thin enough to provide sufficient flexibility for bending about a typewriter platen and at the same time having suflicient strength to maintain dimensional stability for at least the number of copies to be produced therefrom.
- the base stock comprises paper or other sheet stock of fibrous character ordinarily having a high degree of water absorption
- materials such as a resinous solution of melamine-formaldehyde or other suitable wet strength resins. Any high quality of paper base stock can be used in the practice of this invention.
- the method of drying the applied coating is an essential feature of reducing migration of adhesive, as well as the limitation of coat weight and solids content. After application of the coating composition, the latter must be dried in a manner so as to inhibit adhesive migration during drying or the beneficial results of the specified coat weight and solids content will be largely lost. It has been found in accordance with the present invention that evaporation of the liquid portion of the coating must be effected without direct contact of the drying means to the surface of the coating. Drying from the coated side of the base either by means of contact with heated surfaces or heated air should be avoided as such means tend to increase the adhesive migration and increase accumulation of adhesive on the exposed surface of the lithographic plate.
- radiant energy driers such as for example,
- infra-red driers preferably located above the upper surface of the coating on a suitable base, used either alone or in combination with heated drum driers located on the uncoated side of the coated base are preferred for the method of this invention.
- heated drum driers it is essential that the wet coating be dried to a substantially non-tacky condition before the outer ,surface of the coating comes into contact with the heated drum. When this stage is reached, adhesive migration can no longer take place and completion of the drying can be effected by any conventional means.
- Example 1 A lithographic coating was prepared using'the following composition:
- ingredients are designated in parts by weight of dry solids, except where indicated to the contrary.
- the above lithographic coating composition was prepared by mixing of pigments (clay and zinc oxide), dispersing agent (sodium hexametaphosphate) together with about one-third of the polyacrylic acid and enough water to produce a thick paste.
- the polyacrylic acid was added slowly as a 27% solution of the acid in water allowing sufiicient time for the acid to react completely with the zinc oxide pigment.
- the remaining polyacrylic acid solution was then added to the composition.
- the zinc acetate was dissolved in the ammonium hydroxide and the resulting solution mixed with the above composition, the resulting mixture then diluted with water to about 48% solids content.
- the above composition was then applied by a blade coater at a speed of approximately 700 feet/minute onto a high wet strength paper base sheet with a coating weight of about 6 pounds per 3300 square feet of surface. Thereafter, the coated paper was dried by infra-red heat as above described and subsequently calendered. Upon drying, the hydrophilic colloid became highly insoluble, pos. sibly by reason of the fact that upon elimination of the ammonia by volatilization, an insoluble zinc salt of polyacrylic acid was formed.
- the resulting surface was highly receptive to water so that it substantially immediately wet out and yet without further treatment was capable of receiving and holding an ink-receptive, oleophilic imaging material, applied by various means, commonly used in the imaging of conventional lithographic materials.
- the lithographic surface formed on the paper base sheet did not cause excessive stiffening or embrittlement of the base sheet so that the composite structure could be readily used in a typewriter or the like for imaging in the usual manner for office duplication.
- the surface formed upon the drying of the coating composition was insoluble and yet was readily wet out by water in the non-imaging areas and became ink receptive in the areas imaged with the greasy composition or the like..
- the lithographic surface prepared in accordance with the present invention required no brushing and/or treatment of the coated surface with a polyvalent metal salt before it would give satisfactory lithographic reproductions.
- Example 1 Approximately 4 pounds per 3300 square feet of dry solids of the lithographic coating composition of Example 1 was then applied over the base coat by means of a blade coater and subsequently dried as described in Example 1 with the exception that a combination of infra-red heating rays and heated drum driers was used, the coating surface not being permitted to come into contact with the drum driers until after being dried to a non-tacky condition.
- Paper base masters were prepared as described in Example 2 and then coated with the following lithographic coating composition:
- Example 3 4 5 Coating clay 62 62 62 Zinc oxide 26 26 26 Ammonia neutralized polyacrylic 11 12. 5 Sodium hexamotaphosphate- 0. 13 0. 13 0. 13 Zinc acetate 4. 6 4. 6 4. 6 Ammonium hydroxide (26 Banme) 10.8 10. 8 10. 8
- Example 4 was slightly lower than that of Example 2 but better than that of Example 3. That of Example 5 was approximately equal in quality to that of Example 2.
- Example 6-13 Using the process of Example 2, drying of the lithographic coating on the paper base master was accomplished using (1) infra-red heat applied directly on the coated surface of the paper, (2) drum driers contacting the uncoated side of the base, and (3) high velocity air applied to the coated or exposed lithographic surface of the sheet.
- An ink smear test was made by rubbing a standard offset ink on the lithographic surface of the test papers from Examples 6 through 13.
- the ink was diluted 1 pound of ink to 4 parts of ink varnish to reduce the ink viscosity. After removing the excess ink by wiping with a cloth, the test surface was wiped with a cloth ⁇ vetted with standard lithographic etch solution, and G.E. paper brightness tests were made on the test surface. The results are relative with the lower brightness readings indicating better anchorage of the offset ink images.
- Example 14 High sized wet strength paper having approximately 50% long fiber and 50% short fiber, tub sized to seal the paper surface, was given a base coating comprising melamine formaldehyde, starch, clay and zinc oxide applied to paper.
- the components of the base coat were mixed and thereafter applied by means of a blade coater.
- the first base coat was applied with a coat weight of about 8 pounds of dry solids of coating ingredients per 3300 square feet and thereafter a second coating of the same composition and having a coat weight of about 3-4 pounds of dry solids of coating ingredients per 3300 square feet was applied over the first base coat.
- Example 1 The lithographic coating composition of Example 1 was then applied by a blade coater over the second base coat in a coat weight ranging between 1 and 5 pounds of dry solids of coating ingredients per 3300 square feet. After drying as described in Example 13, the dried coated paper was machine calendered. The results with this paper were comparable to those obtained in Examples 2-5.
- the improvement which comprises applying to said paper base an aqueous coating composition of 50-70%, by weight, solids content, and at a rate such as to give a dry coat weight of the order of 1 to 6 pounds per 3300 square feet, comprising inert filler, poiyacrylic acid, and a metal base selected from the group consisting of oxides and hydroxides of zinc, magnesium, calcium, lead and barium, and mixtures thereof, and ammonium ions in an amount in excess of that required to maintain the solubility of the poiyacrylic acid in the presence of the metal by evaporating the water content thereof Within the body 5 of said coating away from the exposed surface thereof.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
- Paints Or Removers (AREA)
Description
United States Patent Oflice 3,415,187 Patented Dec. 10, 1968 3,415,187 LITHOGRAPHIC PLATE AND METHOD FOR MANUFACTURING SAME Burton P. Bailey, Dayton, and Arne E. Gomsi, Chillicothe, Ohio, assignors to The Mead Corporation, Dayton, Ohio, a corporation of Ohio N Drawing. Continuation-impart of application Ser. No. 549,061, May 10, 1966. This application Mar. 16, 1967, Ser. No. 623,555
4 Claims. (Cl. 101-463) ABSTRACT OF THE DISCLOSURE conventionally prepared lithographic plates are subject to several disadvantages and particularly to lack of uniformity of the printing surfaces unless the lithographic surfaces are subjected to a special treatment before use to remove surface defects. These surface defects are usually the result of the accumulation of excess adhesive on the surface of the plate, caused by migration of adhesive to the exposed surface during the drying of the lithographic coating. Applicants have discovered that by effecting drying in a manner such that evaporation of the liquid solvent for the adhesive in the coating composition is accomplished substantially within the coating in a region away from rather than at the exposed surface thereof, the migration of the adhesive to the exposed surface of the drying coating is reduced to such an extent that uniform reproductions can be obtained from the plate without the necessity of additional treatment customarily required.
This is a continuation-in-partapplication of U.S. patent application Ser. No. 549,061 filed May 10, 1966, now abandoned, which was, in turn, a continuation-in-part of U.S. application Ser. No. 413,057 filed Nov. 23, 1964, and now abandoned.
Field of the invention The present invention relates to the preparation of new and improved surfaces having lithographic properties. More particularly, it rel-ates to lithographic plates of improved characteristics and to methods of producing same by reducing mi ration of adhesives used therein to the exposed surface of the coating before and during drying.
Prior art Lithographic surfaces have previously been prepared by applying to suitable carriers, such as paper, coating compositions comprising casein and ester gum to function as a Water receptive hydrophilic colloid, inert fillers such as clay, and formaldehyde. Such coatings were applied in one or more layers depending upon the number of copies to be made from the lithographic plate. Fol-lowing application and drying of the coating, it was necessary for the outer or exposed surface of the coating to be then subjected to a subsequent treatment in order to render the surface suitable for the production of uniform reproductions. Such subsequent treatment usually consisted of brushing or abrading the surface to remove excessive adhesive, or the insolubilization thereof by application of a wash coat comprising a solution of a polyvalent metal, such as a solution of aluminum chloride, zinc chloride, aluminum form-ate, or the like.
When it was desired to produce a long run lithographic plate, ithas been the custom to pre-treat the paper base in order to render it substantially water resistant by applying" to the surface of the' 'paper a resinous varnish, such as phenol-formaldehyde varnish, a urea-formaldehyde solution, a melamine-formaldehyde solution, or the like. The application of such water resistant materials to the paper base, however, makes the latter less receptive to the application of hydrophilic coatings and has thus required' an intermediate coat: in order to insure satisfactory anchoring of the coating to the fibrous base sheet. In producing lithographic plates by prior art processes, it has thus been necessary to apply from five to seven, or even more, coats to produce a suitable lithographic plate on paper, or the like, bases.
During printing with a lithographic plate, it is necessary to apply to the plate an aqueous etch solution. If the base of the plate is an inexpensive paper, such as kraft, the paper to swell and change dimensions as the water application of water to the plate has a tendency to cause penetrates the surface coating and reaches the paper base. Such changes cause distortion: of the image, imperfect registration and deterioration of the paper base. Accordingly, "when the inked lithographic plate is pressed against the rubber mat of the ofiset copying machine, the ink which "is on the image area willcome off onto the blanket while the areas in contact with the non-image areas will remain clear, since the latter areas of the plate are wet only with water and have no ink on them. The blanket is then pressed against a paper sheet to transfer the ink image .to the paper.
When the aqueous etch solution added to the plate penetrates into the body of the plate, the surface of the plate may not be completely wetted by the solution because of the fact that it has been withdrawn from the surface into the plate. When this occurs, the surface of the plate may not repel the printing ink and hence areas of the surface which should be perfectly blank will show backgrdimd discoloration or become darkened or toned. This iiiomplete wetting of the surface of the plate may also occpr during printing.
If water penetrates the surface of the hydrophilic surface coating and renders the coating soluble under the image ar'i'as, the image will no longer hold onto the plate and tends to leave the printing surface. Yet, on the other hand, if the surface is so highly resistant to the imaging material that it fails to adhere properly, the same thing occurs. The material forming the image must adhere tenaciously to the plate and not come off either wholly or in part or be destroyed by successive transfers from the image area. Attempts have been ,made to overcome these difiic-ulties by interposing a resinous water barrier between the paper base and the surface coating but this does not prevent water from being drawn from the surface into the coating layers above the barrier surface.
It is important that the adhesive employed for holding the coating onto the base be of such character that it satisfactorily bonds the coating layer and at the same time is subject to a minimum tendency to migrate to the outer or exposed surface of the coating, or into the base stock during the drying operation. Migration of the adhesive to the outer surface of the lithographic plate causes an undue accumulation of adhesive on the surface and seals the latter, thereby preventing the imaging material from penetrating the surface and firmly anchoring thereto. On the other hand, migration of adhesive into the base stock produces a surface layer relatively low in adhesive content and not sufficiently bonded to anchor the image.
Some of the difficulties of the prior art have been overcome by the procedure disclosed in Beatty U.S. Patent No. 2,760,431. While the method of the latter patent represents an improvement over prior processes in that saiisfactory lithographic reproductions are obtained with a fewer number of coats, the Beatty method is still subject to the disadvantage of not giving consistent uniform printing results unless lithographic plates as produced are subjected to a subsequent treatment before use in order to remove excessive amounts of adhesive which have migrated to the outer surface of the plate. In order, therefore, to obtain satisfactory results when using the Beatty lithographic plates, it is necessary to subject them before use to a brushing or abrading treatment in order to remove mechanically the excess adhesive accumulated on the outer surface of the plate, or to wash the plates with a solution of a polyvalent metal salt. Applicants improved process obviates the necessity for this subsequent step by effecting the drying of the lithographic plates in a manner such that substantial migration of the adhesive to the surface does not take place.
Summary and objects Accordingly, 'an object of the present invention is to provide means for obviating the difliculties previously inherent in paper base lithographic plates.
Another object is to produce and to provide a method for producing a new and improved lithographic surface using high speed coating techniques.
Still another object is to produce and to provide a method for producing a lithographic plate of the type described which requires consider-ably fewer operational steps in its manufacture and which during use is capable of holding an ink-receptive image having the properties of immediate reproduction of copy of good quality.
Another object is to provide a method of controlling adhesive migration during application of lithographic coatings to a paper base.
Yet another object is to produce and to provide a method for producing a paper base lithographic plate of the character described which is useful either as a direct image master or as an indirect image master where the existing image produced elsewhere is transferred to a coating surface produced in accordance with the invention.
A further object is to produce an improved lithographic plate of the type described which is easy and economical to manufacture and use, is characterized by excellent stability, is capable of holding tenaciously an inkreceptive image having the properties of immediate reproduction of copy of good quality and which continues to produce such copies for a considerable period of time.
Description The process of the present invention relates to a method for effecting the drying of lithographic plates, and particularly paper base lithographic plates, in a manner so as to substantially reduce migration of the adhesive content to the exposed surface of the coating during said drying operation. More specifically, it relates to an improvement of the product and process of Beatty US. Patent 2,760,431, referred to above. Applicants have discovered that by effecting drying of the Beatty coating in the manner discovered by them and specifically described below, consistent and uniform printing results can be obtained without resorting to the added step of brushing or abrading or washing with a solution of a polyvalent metal salt, as required when plates are produced as described by Beatty.
The Beatty product is obtained by coating a base with a composition containing an inert filler, polyacrylic acid and a metal base selected from the group consisting of the oxides and hydroxides of zinc, magnesium, calcium, barium and lead, and mixtures thereof, and present in the ratio of 1 part by weight of metal base to 2-20 parts by weight of filler and 1 part by weight of polyacrylic acid to 2-10 parts by weight filler plus metal base and with ammonium ions present in amounts in excess of that necessary to maintain the solubility of the polyacrylic acid in the presence of the metal base. The resulting composition in the form of 40-60% solids content with water was coated onto a suitable base in an amount sufficient to give a coating weight of 6-30 pounds per 3300 square feet surface and then dried by passage through an air drying oven heated to a temperature in excess of 250 F. The lithographic plates thus produced required treatment by brushing or abrasion or washing with a solution of a polyvalent metal salt before consistent lithographic printing results were obtainable.
Applicants have discovered that the subsequent brushing, abrading or washing step is not required for satisfactory lithographic printing results if the lithographic coating is subjected to a drying operation whereby the migration of adhesive to the outer or exposed coating surface is reduced to a minimum. They have also discovered that this type of drying can be accomplished in different manners so long as the solvent for the adhesive (water plus ammonia) is evaporated substantially within the coating and principally at the coating base sheet interface rather than at the exposed surface of the coating. In other words, evaporation of the liquid solvent must be effected substantially in a region within said coating away from the exposed coating surface. In order to accomplish this, severe drying conditions must not be directly applied to the exposed surface of the coating until the drying has been effected to such a degree that the coating is nontacky, at which point further migration of adhesive does not take place. Contact of the drying coating surface with heated drying or casting drums or hot or cold high velocity (impinging) dry air is to be avoided. After immobilization of the liquid portion of the coating, the form of drying becomes of much less importance.
Applicants have found that evaporation of solvent in the coating composition is most satisfactorily effected by use of infra-red rays or by application of heat to the uncoated side of the coated base, such as by contacting the uncoated surface of the base with a dryer drum. Yankee dryer or impinging hot air. Since heat is generated throughout the coated paper by absorption of the infra-red rays, these rays may be applied from either the uncoated or the coated side of the base. In any event, it is highly important to the success of the present invention that heat not be applied to the outer or exposed coating surface until after the coating has dried to a substantially non-tacky state, whereby the liquid portion of the coating is immobilized. When heat is applied directly to the exposed surface, the liquid solvent and adhesive first migrate to the surface where evaporation of the solvent takes place and thereby permitting an 'accumulation of adhesive at the lithographic surface. Using the method of drying of this invention, evaporation takes place substantially Within the coating and at the coatingbase interface, thus reducing accumulation of adhesive at the lithographic surface.
The migration of adhesive to the lithographic surface 'is also affected by such factors as the character of the adhesive, the quantity thereof used in the coating, the coat weight, the solids content of the coating, as well as the method of drying. For example, migration of adhesive is reduced by using a lower coat weight and a higher solids content than customarily employed, as well as by effecting the drying of the wet coating by the method of this invention. While each of these factors is important, the most satisfactory general results are obtained by the use of a combination of these factors.
The coat weight used should be sufficient to form a continuous lithographic surface but should not be so heavy as to cause cracking of the coating. -In addition to providing poor coverage over the base coat, insufficient coat weight results in short copy life. Excess coat weights, in addition to causing increased adhesive'migration, cause surface cracking which results in reproduction of the cracks on the copy and also in short copy life.
The proper coat weight employed will depend to some extent upon the composition of the paper base which, in turn, depends upon the desired copy life. For example, tests have shown that a paper raw stock which has been tub sized and then given two base coats should preferably use a coat weight ranging from one to five pounds per 3300 square feet. Generally, a four pound coat has given optimum results, other critical factors being the same. However, acceptable levels of lithographic surfaces have been obtained outside this range.
It has been discovered in accordance with the present invention that adhesive migration is reduced and copy life improved when the solids content of the coating is maintained at in excess of 50% and preferably at from 50 to 70% by weight of the total weight of the coating composition. The upper solids content limit appears to be determined primarily by handling problems. The higher solids content reduces the drying load as well as minimizes adhesive migration and, at the same time, gives better copy life. The latter results are particularly significant with application of lower coat weights where adhesive migration is minimized since the total water or other carrier fluid in the coating is much lower. When the solids content is reduced below 50%, excessive adhesive migration is observed. Commercially satisfactory results have been obtained in accordance with the present invention by use of high solids content with lower coat weight when drying of the applied coating is effected as hereinabove specified.
In addition to clay, the inert filler can include such materials as chalk, talc, satin white, silica, and the like.
The various constituents of the coating should preferably be present within certain specified ranges. For example, the zinc oxide and adhesive should preferably be present in the ratio of 1 part adhesive to 1-4 parts of zinc oxide. The zinc oxide and inert filler are preferably present in the ratio of part zinc oxide to 2 parts inert filler. The ratio of adhesive to zinc oxide plus inert filler is preferably 1 to 2 parts polyacrylic acid to parts of zinc oxide plus inert filler.
Suitable supports for the lithographic surface can include paper, fiberboard, textile fabrics, plastic sheet stock or metal strips, preferably thin enough to provide sufficient flexibility for bending about a typewriter platen and at the same time having suflicient strength to maintain dimensional stability for at least the number of copies to be produced therefrom.
When a fairly large number of copies is desired and the base stock comprises paper or other sheet stock of fibrous character ordinarily having a high degree of water absorption, it is desirable to introduce high wet strength into the base stock by known pre-treatment with materials such as a resinous solution of melamine-formaldehyde or other suitable wet strength resins. Any high quality of paper base stock can be used in the practice of this invention.
' The method of drying the applied coating is an essential feature of reducing migration of adhesive, as well as the limitation of coat weight and solids content. After application of the coating composition, the latter must be dried in a manner so as to inhibit adhesive migration during drying or the beneficial results of the specified coat weight and solids content will be largely lost. It has been found in accordance with the present invention that evaporation of the liquid portion of the coating must be effected without direct contact of the drying means to the surface of the coating. Drying from the coated side of the base either by means of contact with heated surfaces or heated air should be avoided as such means tend to increase the adhesive migration and increase accumulation of adhesive on the exposed surface of the lithographic plate. Excellent results with substantially no adhesive migration to the lithographic surface have been obtained by effecting drying of the coated base (1) applying heat to the uncoated side thereof or by (2) radiant energy driers from either or both sides of the coated base, by (3) dielectric heat energy (high frequency) driers, or by (4) any combination of (1), (2), and (3).
The use of radiant energy driers, such as for example,
infra-red driers, preferably located above the upper surface of the coating on a suitable base, used either alone or in combination with heated drum driers located on the uncoated side of the coated base are preferred for the method of this invention. Where a series of heated drum driers is used, it is essential that the wet coating be dried to a substantially non-tacky condition before the outer ,surface of the coating comes into contact with the heated drum. When this stage is reached, adhesive migration can no longer take place and completion of the drying can be effected by any conventional means.
The following examples are given to further illustrate the claimed invention. However, it will be evident that numerous modifications and changes can be made in these examples without materially modifying the results obtained. Any such modifications and changes which do not depart from the basic concept of the invention disclosed herein are intended to fall within the scope of the appended claims.
Example 1 A lithographic coating was prepared using'the following composition:
In the above composition, as well as in the examples to follow, the ingredients are designated in parts by weight of dry solids, except where indicated to the contrary.
The above lithographic coating composition was prepared by mixing of pigments (clay and zinc oxide), dispersing agent (sodium hexametaphosphate) together with about one-third of the polyacrylic acid and enough water to produce a thick paste. The polyacrylic acid was added slowly as a 27% solution of the acid in water allowing sufiicient time for the acid to react completely with the zinc oxide pigment. The remaining polyacrylic acid solution was then added to the composition. The zinc acetate was dissolved in the ammonium hydroxide and the resulting solution mixed with the above composition, the resulting mixture then diluted with water to about 48% solids content.
The above composition was then applied by a blade coater at a speed of approximately 700 feet/minute onto a high wet strength paper base sheet with a coating weight of about 6 pounds per 3300 square feet of surface. Thereafter, the coated paper was dried by infra-red heat as above described and subsequently calendered. Upon drying, the hydrophilic colloid became highly insoluble, pos. sibly by reason of the fact that upon elimination of the ammonia by volatilization, an insoluble zinc salt of polyacrylic acid was formed.
The resulting surface was highly receptive to water so that it substantially immediately wet out and yet without further treatment was capable of receiving and holding an ink-receptive, oleophilic imaging material, applied by various means, commonly used in the imaging of conventional lithographic materials.
The lithographic surface formed on the paper base sheet did not cause excessive stiffening or embrittlement of the base sheet so that the composite structure could be readily used in a typewriter or the like for imaging in the usual manner for office duplication. As noted heretofore, the surface formed upon the drying of the coating composition was insoluble and yet was readily wet out by water in the non-imaging areas and became ink receptive in the areas imaged with the greasy composition or the like..Unlike prior art lithographic surfaces made by other methods, the lithographic surface prepared in accordance with the present invention required no brushing and/or treatment of the coated surface with a polyvalent metal salt before it would give satisfactory lithographic reproductions.
Example 2 Parts Coating clay 55 Zinc oxide 22 Sodium hexametaphosphate 0.5 Starch 23 Melamine resin 9.2
Approximately 4 pounds per 3300 square feet of dry solids of the lithographic coating composition of Example 1 was then applied over the base coat by means of a blade coater and subsequently dried as described in Example 1 with the exception that a combination of infra-red heating rays and heated drum driers was used, the coating surface not being permitted to come into contact with the drum driers until after being dried to a non-tacky condition.
After calendering, the sheet prepared as above described was used as an offset master with excellent results. Typewritten characters were consistently reproduced in excellent detail without background discoloration in excess of 300 copies in each test, and easily readable copies were obtained even after the 2500th copy.
Examples 3, 4,
Paper base masters were prepared as described in Example 2 and then coated with the following lithographic coating composition:
Example 3 4 5 Coating clay 62 62 62 Zinc oxide 26 26 26 Ammonia neutralized polyacrylic 11 12. 5 Sodium hexamotaphosphate- 0. 13 0. 13 0. 13 Zinc acetate 4. 6 4. 6 4. 6 Ammonium hydroxide (26 Banme) 10.8 10. 8 10. 8
Example 4 was slightly lower than that of Example 2 but better than that of Example 3. That of Example 5 was approximately equal in quality to that of Example 2.
All masters of Examples 2, 3, 4 consistently reproduced in excellent detail at least 300 copies and had no observable background discoloration. As in Example 2, easily readable copies were obtained even after the 2500th copy. It is to be noted that when adhesive content was reduced to 9 parts, the image was lifted after a relatively few copies and when adhesive content was increased to 13 parts, a typed image did not bond well to the lithographic surface.
Examples 6-13 Using the process of Example 2, drying of the lithographic coating on the paper base master was accomplished using (1) infra-red heat applied directly on the coated surface of the paper, (2) drum driers contacting the uncoated side of the base, and (3) high velocity air applied to the coated or exposed lithographic surface of the sheet. The relative results, as determined by the number of satisfactory copies produced, were as follows:
Infra-red Drum High Copy Ink gas temp., velocity results smear burners F. air, F tests l Example 6.. 05.. 300 NA 77.3 Example 7. On.. 75 300 NA 74. 6 Example 8.. OIL. 75 75 NA 75.4 Example 9 On 75 Off Excellent 53.9 Example 10... n 200 300 A 76. 0 Example 11... Off 200 300 NA 78.1 Example 12... O5 200 Off Fair to good... 63. 4 Example 13... On 200 011 Excellent 48.4
An ink smear test was made by rubbing a standard offset ink on the lithographic surface of the test papers from Examples 6 through 13. The ink was diluted 1 pound of ink to 4 parts of ink varnish to reduce the ink viscosity. After removing the excess ink by wiping with a cloth, the test surface was wiped with a cloth \vetted with standard lithographic etch solution, and G.E. paper brightness tests were made on the test surface. The results are relative with the lower brightness readings indicating better anchorage of the offset ink images.
NA-Not acceptable.
Example 14 'High sized wet strength paper having approximately 50% long fiber and 50% short fiber, tub sized to seal the paper surface, was given a base coating comprising melamine formaldehyde, starch, clay and zinc oxide applied to paper. The components of the base coat were mixed and thereafter applied by means of a blade coater. The first base coat was applied with a coat weight of about 8 pounds of dry solids of coating ingredients per 3300 square feet and thereafter a second coating of the same composition and having a coat weight of about 3-4 pounds of dry solids of coating ingredients per 3300 square feet was applied over the first base coat. The lithographic coating composition of Example 1 was then applied by a blade coater over the second base coat in a coat weight ranging between 1 and 5 pounds of dry solids of coating ingredients per 3300 square feet. After drying as described in Example 13, the dried coated paper was machine calendered. The results with this paper were comparable to those obtained in Examples 2-5.
What is claimed is:
1. In the process of producing improved lithographic plates by reducing the accumulation of multivalent metal poiyacrylic adhesives at the exposed surfaces of lithographic printing plates during drying on a paper base, the improvement which comprises applying to said paper base an aqueous coating composition of 50-70%, by weight, solids content, and at a rate such as to give a dry coat weight of the order of 1 to 6 pounds per 3300 square feet, comprising inert filler, poiyacrylic acid, and a metal base selected from the group consisting of oxides and hydroxides of zinc, magnesium, calcium, lead and barium, and mixtures thereof, and ammonium ions in an amount in excess of that required to maintain the solubility of the poiyacrylic acid in the presence of the metal by evaporating the water content thereof Within the body 5 of said coating away from the exposed surface thereof.
2. The process of claim 1 wherein said evaporation is eifected by means of infra-red heat.
3. The process of claim 1 wherein said evaporation is efiected by heating means contacting the uncoated side of said base sheet.
4. The process of claim 1 wherein said evaporation is effected by infra-red heat followed by drum dryers contacting the uncoated side of said base sheet.
References Cited UNITED STATES PATENTS 2/1951 Van Dusen 101-460 *6/1952 Beatty 101-462 XR 10/ 195-6 Halpern et a1. 101-462 l/1966 Hetfner 101-462 DAVID KLEIN, Primary Examiner.
US. Cl. X.R.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR38715A FR1459454A (en) | 1964-11-23 | 1965-11-17 | Process for preparing a lithographic plate |
| GB49040/65A GB1121868A (en) | 1964-11-23 | 1965-11-18 | Lithographic plate and method of manufacturing same |
| BE672558D BE672558A (en) | 1964-11-23 | 1965-11-19 | |
| DE19651546789 DE1546789A1 (en) | 1964-11-23 | 1965-11-22 | Lithographic printing plate and method for making it |
| NL6515162A NL6515162A (en) | 1964-11-23 | 1965-11-23 | |
| US623555A US3415187A (en) | 1964-11-23 | 1967-03-16 | Lithographic plate and method for manufacturing same |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41305764A | 1964-11-23 | 1964-11-23 | |
| US623555A US3415187A (en) | 1964-11-23 | 1967-03-16 | Lithographic plate and method for manufacturing same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3415187A true US3415187A (en) | 1968-12-10 |
Family
ID=27022049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US623555A Expired - Lifetime US3415187A (en) | 1964-11-23 | 1967-03-16 | Lithographic plate and method for manufacturing same |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3415187A (en) |
| BE (1) | BE672558A (en) |
| DE (1) | DE1546789A1 (en) |
| GB (1) | GB1121868A (en) |
| NL (1) | NL6515162A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6067190A (en) * | 1983-09-22 | 1985-04-17 | Ricoh Co Ltd | Ink jet recording medium |
| GB9804743D0 (en) * | 1998-03-06 | 1998-04-29 | Horsell Graphic Ind Ltd | Printing |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2542784A (en) * | 1945-09-21 | 1951-02-20 | Addressograph Multigraph | Planographic printing plate and method of preparing the same |
| US2760431A (en) * | 1952-06-19 | 1956-08-28 | Dick Co Ab | Lithographic plates and methods for manufacturing same |
| US2766688A (en) * | 1951-03-06 | 1956-10-16 | Polychrome Corp | Planographic printing plate |
| US3228327A (en) * | 1962-04-05 | 1966-01-11 | Kvp Sutherland Paper Co | Multipurpose duplicating master |
-
1965
- 1965-11-18 GB GB49040/65A patent/GB1121868A/en not_active Expired
- 1965-11-19 BE BE672558D patent/BE672558A/xx unknown
- 1965-11-22 DE DE19651546789 patent/DE1546789A1/en active Pending
- 1965-11-23 NL NL6515162A patent/NL6515162A/xx unknown
-
1967
- 1967-03-16 US US623555A patent/US3415187A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2542784A (en) * | 1945-09-21 | 1951-02-20 | Addressograph Multigraph | Planographic printing plate and method of preparing the same |
| US2766688A (en) * | 1951-03-06 | 1956-10-16 | Polychrome Corp | Planographic printing plate |
| US2760431A (en) * | 1952-06-19 | 1956-08-28 | Dick Co Ab | Lithographic plates and methods for manufacturing same |
| US3228327A (en) * | 1962-04-05 | 1966-01-11 | Kvp Sutherland Paper Co | Multipurpose duplicating master |
Also Published As
| Publication number | Publication date |
|---|---|
| BE672558A (en) | 1966-05-20 |
| DE1546789A1 (en) | 1970-10-08 |
| GB1121868A (en) | 1968-07-31 |
| NL6515162A (en) | 1966-05-24 |
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