US3181460A - Paper offset plate for photographic transfer and direct image printing - Google Patents

Paper offset plate for photographic transfer and direct image printing Download PDF

Info

Publication number
US3181460A
US3181460A US6839A US683960A US3181460A US 3181460 A US3181460 A US 3181460A US 6839 A US6839 A US 6839A US 683960 A US683960 A US 683960A US 3181460 A US3181460 A US 3181460A
Authority
US
United States
Prior art keywords
water
polyamide
parts
image
planographic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US6839A
Inventor
Glenn H Perkins
Loring W Mcfail
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Oxford Paper Co
Original Assignee
Oxford Paper Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Oxford Paper Co filed Critical Oxford Paper Co
Priority to US6839A priority Critical patent/US3181460A/en
Priority to GB36190/60A priority patent/GB956376A/en
Priority to DEO7847A priority patent/DE1216896B/en
Priority to FR851625A priority patent/FR1278588A/en
Application granted granted Critical
Publication of US3181460A publication Critical patent/US3181460A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41NPRINTING 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
    • B41N3/00Preparing for use and conserving printing surfaces
    • B41N3/03Chemical or electrical pretreatment

Definitions

  • United States Patent Thisinvention relates to planographic printing plates and the method of making the same. More particularly, the invention relates to printing plates formed by coating a suitable base with a coating composition comprising a pigment, a hydrophilic colloid, and a water-soluble cationic thcrmosetting resin, and insolubilizing said composition upon the base.
  • Ofiset or planographic printing plates are used to repro- :luce images which have been applied to the pla-nographic surface of the plate.
  • the image is oleophilic in nature in that it attracts oily or greasy substances and is essen-J tially water repellent.
  • the unirnaged portion of the planographic surface is hydrophilic to the extent that it :an easily be wet by water but it can also, before wetting, accept and hold an oily or greasy image.
  • planographic sur- Face thus prepared and imaged is subjected to treatment 1y an etch solution which prepares the plate for printing. lhe etch solution is repelled by the image portion of the :late but is attracted by the unimaged area. The unmaged area, therefore, is covered by a surface film of :tch solution leaving the image portion alone ink re- :eptive.
  • a planographic printing plate thus prepared can operate on an oflset printing press whereby the plate is alernatively contacted by a roll supplying-water and a roll :upplying ink. After the image has been inked, it is ransferred from the plate to a rubber blanket and from he blanket to the copy paper.
  • the printing plates produced according to this invenion are prepared by self-insolubilization methods and hese plates possess an excellent hydrophilic-oleophilic valance permitting good image adherence and good image ife while at the same time permitting good water (or tch solution) retention.
  • Planographic surfaces prepared s disclosed herein produce clean copy, good toning, and ossess good image, correction life, and stop-go" roperties.
  • the printing plates of this invention are of articular value not only in that they may be employed 1 a conventional Direct Image reproduction process as escribed above, but these plates can advantageously e employed in the Verifax (Eastman) process. Veriax is a trade name of the Eastman Kodak Company for hotocopying apparatus and photographic processing hemicals for use in offiee photocopying apparatus.
  • Verifax Matrix Paper with n emulsion In the Verifax process, a Verifax Matrix Paper with n emulsion is employed.
  • the emulsion of Verifax latrix Paper is composed of a suspension of silver halide, eveloper and dye-forming components.
  • the matx When the matx is exposed in the copier, the light reaches the emulsion rrough the matrix paper stock.
  • the emulsion in contact ith the clear areas .of the document receives the greatit amount of light. After about seconds in the activarr, these fully exposed areas are hardened so much that my adhere to the matrix and do not transfer.
  • the parally exposed areas are dyed and zrtially developed, but not hardened.
  • the matrix then squeegeed and rolled in contact with Verifax opy Paper, or other suitable commercial paper, a layer the unhardened dyed material, which is still in a gelatinous state, is transferred to the copy paper.
  • Verifax opy Paper or other suitable commercial paper
  • the lower layers of unhardened matrix material are successively transferred to sheets of copy paper.
  • white areas of the copies stay white because little, if any, material is transferred to them.
  • the image is expected to stabilize to a brown color after some time, but will remain as legible as other business papers.
  • the printing plates of this invention may also advantageously be employed in the Ektalith (Eastman) process.
  • Ektalith is a trade name of Eastman Kodak Company for photocopying process and apparatus.
  • the invention consists of forming an aqueous coating composition comprising a pigment, a hydrophilic colloid and a water-soluble cationic thermosetting resin.
  • This aqueous coating composition is then applied in a conventional manner to the surface desired, usually a wet strength paper web, and the coating dried, advantageously at a pH of about 7.0, to effect a cross-linking of the hydrophilic colloid and the water-soluble cationic thermosetting resin to form an insoluble hydrophilic planographic surface.
  • thermosetting resins which may be employed in the practice of this invention are wet strength resins manufactured by Hercules Powder Company under the trade (name Kyrnene 557. These water-soluble cationic thermosetting resins and the methods of making them are described in detail in United States Patent No. 2,926,154.
  • These resins are prepared by reacting a saturated aliphatic dicarboxylic acid with a polyalkylene polyamine to form a long chain water-soluble polyamide, and then reacting the polyamide with epichlorohydrin to form a Water-soluble cationic thermosetting resin.
  • a resin which may advantageously be employed is prepared byreacting a saturated aliphatic dicarboxylic acid containing 3 to 8 carbon atoms with from about 0.8 to about 1.4 moles, per mole of dicarboxylic acid, of a polyalkylene poly amine to form a long chain water-soluble polyamide, and then reacting the polyamide with epichlorohydrin in a mole ratio of epichlorohydrin to secondary amine groups of the polyamide of from about 0.5 to 1 to about 1.8 to l to form a water-soluble cationic thermosetting resin.
  • pigments can be used to form the coating compositions of the printing plates of this invention such as silica, calcium silicate, barium sulfate, titanium dioxide, and clays such as kaolin, e.g. Lustra Clay. Lustra Clay is marketed by the Southern Clay Company. The pigments may be used as a mixture if desired.
  • An example of a combined pigment which has been found to be advantageous is a mixture of about 40% by weight of colloidal silica to about 60% by weight of Lustra Clay.
  • the colloidal silica which can be used according to this invention should contain silica particles of very small size.
  • the main average size of the silica particles should be within a range of from about 7 millimicrons to about 30 millimicrons.
  • colloidal silicas containing silica particles of less than 7 millimicrons have not been commercially available, it is believed that the coating compositions of this invention may be advantageously prepared from colloidal silicas containing silica particles of a size even less than 7 millimicrons.
  • colloidal silicas are those which contain silica particles ranging in size from about 7 to 17 millimicrons.
  • colloidal silicas are marketed by E. I. du Pont de Nemoursand Company under thetradenames Ludox S.M., Ludox L.S., and Ludox HS. and
  • colloidal silicas also by the Monsanto Chemical Company under the trade name Syton 200.
  • Syton 200 The types of colloidal silicas and methods of making them are described in detail in United- States Patents No. 2,244,325 issued June 3, 1941, 2,574,- 902 issued November 13, l951,and 2,597,872-issued May 27, 1952.v
  • colloidal silicas are generally marketed as a 30% SiO solution. but as described in the above patents the colloidal silica can be prepared containing a higher or lower percent silica.
  • Ludox S.M. is desirable as this material "has a particle size of about 7 millimicrons and enables curing of the coating composition to becarried out in a shorter time. Higher machine speeds can also be used in the production of planographic plates using the Ludox S.M.
  • the chlorinated corn starch referred to is an oxidized starch product from common corn starch by treating it in an aqueous suspension with a hypochlorite solution containing a slight excess of sodium hydroxide.
  • Polyvinyl alcohol has been found to be particularly advantageous.
  • the amounts of pigment which can be used can vary quite widely depending upon the particular hydrophilic colloid employed. We have found that a pigment-hydrophilic colloid-ratio of about 2:1 to about 7:1 is generally suitable although both higher and lower ratios can be used. When using sodium carboxymethyl cellulose as the hydrophilic colloid, we have found it to be advantageous to maintain the pigment-colloid ratio about 5:1. Depending upon the hydrophilic colloid employed, the ratio of the Kymene 557 to the colloid may advantageously be from about 30% to about The reaction or cross linking of the hydrophilic colloid with the water-soluble cationic thermosetting resin is advantageously carried out at a pH of approximately 7.0.
  • Salts which may be advantageously used to enhance the planographic properties of the plate include zinc acetate, zinc chloride, zinc phenol sulfonate, zinc sulfamate, zinc silicofluoride, and alum, as well as salts of other divalent and tri-valent metals, e.g. lead, calcium, manganese, cerium, lanthanum.
  • Other suitable salts can, of course, be used.
  • the amount of salt which can be used can be varied widely depending on the particular salt employed. The amount which is utilized can be 4 readily determined by those skilled in the art.
  • Verifax process it is particularly advantageous to em ploy a coating composition having a pH between about 6 to 9.
  • the pH of the coating compositions may be adjusted to the proper pH range by the use of acetic acid, ammonia, morpholine, causticsoda and the like.
  • the coating compositions produced according to this invention are advantageously prepared by first preparing the pigment or pigment mixture, and adding thereto the hydrophilic colloid, while stirring. Next, the watersoluble cationic thermosetting resin is added andthen the salt. The mixing may be done at room temperature and the viscosity of the mixture is advantageously adjusted to about 200 centipoises, Brookfield. The pH can be adjusted by adding ammonia or acetic acid to bring the pH to between 6 and 9 and preferably to about 7.0.
  • the aqueous coating compositions may be applied to a base web or sheet by conventional apparatus, suchas air knives or roll coaters.
  • the amount of coating may vary from about 2 to 10 pounds per ream of 3300 square feet, with 6 to 8 pounds being most satisfactory.
  • the stock is dried at normal festoon dryer temv 7' peratures (e.g. 110 F.l F.) to remove moisture.
  • the stock is then cured by exposure to temperatures of about 325 F.350 F. for a period of 2 to 15 seconds.
  • the curing temperature and the curing time will depend for example upon the type and amount of salt used, the pH of the coating composition, the particular hydrophilic colloid used, etc.
  • the optimum time and planographic printing plates were prepared by coating asuitable wet strength paperstock with the aqueous coating composition described therein, and drying and then curing the applied coatings by exposure to a temperature of about 325 F.-350 F. fora period of about 2-15 seconds.
  • Example I Eighty-four parts of a 6% sodium carboxymethyl cellulose solution were mixed with 26 parts of Lustra Clay (60% suspension) and 32 parts of Syton 200 (30% suspension), 15 parts of Kymene 557 (10% solution), 8 parts zinc acetate (25% solution), and 60 parts water. The pH of the color was adjusted to 6.5 with ammonia. The composition was coated on a paper base and then dried and cured.
  • Example 2 The procedure followed in Example 1 was followed except that 34 parts of a 15% solution of Penford Gum' No. 280 were used in place of the 84 parts sodium car-. boxymethyl cellulose and 30 parts of water were employed instead of 60 parts of water.
  • Penford Gum 280 is a hydroxymethyl starch ether of a low degree of substitution -manufactured by Penick and Ford Ltd.
  • Example 3 Two hundred parts of an 8% solution of a high viscosity, 98% hydrolyzed polyvinyl alcohol, marketed by du Pont under the trade name Elvanol 72-51, were mixed with 83.5 parts of Lustra Clay (60% suspension) and 100 parts of Ludox S.M. (30% suspension), 48 parts higher or lower pH may be i f Kymene 557 solution), 4 parts zinc acetate (in 2 parts water) and 10 parts butyl alcohol. The pH of le color was adjusted to 9 with soda ash. The composion was coated on a paper base and then dried and cured.
  • Example 4 7 Eighty nine parts of a 9% solution of a high viscosity, 3% hydrolyzed polyvinyl alcohol, marketed by du Pont ider the trade name Elvanol 72-51, were mixed with l parts of Lustra Clay (60% suspension) and 50 parts Ludox SM. (30% suspension), 5 parts of a hydrated agnesium aluminum silicate (manufactured by Attapul- 1s Minerals & Chemicals Corp. under the trade name ttasorb RVM), 24 parts of Kymene 557 (10% solution), parts zinc acetate (25% solution) and 5 parts of butyl cohol. The pH of the color was adjusted to 9 with da ash. The composition was coated on a paper base 1d then dried and cured.
  • Lustra Clay 60% suspension
  • Ludox SM. 30% suspension
  • 5 parts of a hydrated agnesium aluminum silicate manufactured by Attapul- 1s Minerals & Chemicals Corp. under the trade name ttasorb RVM
  • the cured coatings of all the printing plates produced shown in Examples 1 through 5 were hard and watersoluble, and they possessed excellent hydrophilic-01cciilic balances. These printing plates were successfully ed in the Direct Image process, the Verifax and the ttalith processes. Employing small amounts of Attarb were found to improve the tooth and image transfer the resulting plates, particularly when the plates were ed in the Verifax and the Ektalith processes.
  • the printing plates of this invention may advantageousbe used in Xerography.
  • Xerography is a non-chemical totographic process in which the plate is sensitized eleccally and developed by dusting with electrically charged re powder. The Xerography process is more generally scribed, for example, in United States Patent No.
  • a planographic printing plate comprising a base and, hered thereto, an insolubilized coating which comprises pigment and the reaction product of a hydrophilic cold and a water-soluble cationic thermosetting resin prered by reacting a saturated aliphatic dicarboxylic acid ntaining 3 to 8 carbon atoms with from about 0.8 to out 1.4 moles, per mole of dicarboxylic acid, of a poly- :ylene polyamine having two primary amine groups dat least one secondary amine group to form a long ain water-soluble polyamide, and then reacting the polylide with epichlorohydrin in a mole ratio of epichlorodrin to secondary amine groups of the polyamide of rm about 0.5 to l to about 1.8 to l.
  • planographic printing plate of claim 1 in which base is a paper base.
  • the hydrophilic colloid is polyvinyl alcohol and in which the pigment contains colloidad silica having a particle size between about 7 and millimicrons.
  • planographic printing plate of claim 4 upon which there is placed an ink-receptive image.
  • planographic printing plate of claim 7 upon 0 which there is placed an ink-receptive image.
  • a method of reproducing an image which comprises placing an ink-receptive image upon a planographic surface of a planographic printing plate having a paper base and a planographic coating adhered thereto comprising a pigment and the reaction product of a hydrophilic colloidand a water-soluble cationic thermosetting resin prepared by reacting a saturated aliphatic dicarboxylic acid containing 3 to 8 carbon atoms with from about 0.8 to about 1.4 moles, per mole of dicarboxylic-acid, of a polyalkylene polyamine having two primary amine groups and at least one secondary amine group to form a long chain water-soluble polyamide, and then reacting the polyamide with epichlorohydrin in a mole ratio of epichlorohydrin to secondary amine groups of the polyamide of from about 0.5 to 1 to about 1.8 to 1, contacting the planographic surface with the ink-receptive image thereon with a roll supplying an aqueous fountain solution, then contacting the planographic surface with the ink-re

Description

United States Patent Thisinvention relates to planographic printing plates and the method of making the same. More particularly, the invention relates to printing plates formed by coating a suitable base with a coating composition comprising a pigment, a hydrophilic colloid, and a water-soluble cationic thcrmosetting resin, and insolubilizing said composition upon the base.
Ofiset or planographic printing plates are used to repro- :luce images which have been applied to the pla-nographic surface of the plate. The image is oleophilic in nature in that it attracts oily or greasy substances and is essen-J tially water repellent. The unirnaged portion of the planographic surface is hydrophilic to the extent that it :an easily be wet by water but it can also, before wetting, accept and hold an oily or greasy image. Planographic iurfacesmust'have this hydrophilic-oleophilic balance so :hat the oily or greasy image can be applied thereto and :he unimaged area wet by water. The planographic sur- Face thus prepared and imaged is subjected to treatment 1y an etch solution which prepares the plate for printing. lhe etch solution is repelled by the image portion of the :late but is attracted by the unimaged area. The unmaged area, therefore, is covered by a surface film of :tch solution leaving the image portion alone ink re- :eptive.
A planographic printing plate thus prepared can operate on an oflset printing press whereby the plate is alernatively contacted by a roll supplying-water and a roll :upplying ink. After the image has been inked, it is ransferred from the plate to a rubber blanket and from he blanket to the copy paper.
The printing plates produced according to this invenion are prepared by self-insolubilization methods and hese plates possess an excellent hydrophilic-oleophilic valance permitting good image adherence and good image ife while at the same time permitting good water (or tch solution) retention. Planographic surfaces prepared s disclosed herein produce clean copy, good toning, and ossess good image, correction life, and stop-go" roperties. The printing plates of this invention are of articular value not only in that they may be employed 1 a conventional Direct Image reproduction process as escribed above, but these plates can advantageously e employed in the Verifax (Eastman) process. Veriax is a trade name of the Eastman Kodak Company for hotocopying apparatus and photographic processing hemicals for use in offiee photocopying apparatus.
In the Verifax process, a Verifax Matrix Paper with n emulsion is employed. The emulsion of Verifax latrix Paper is composed of a suspension of silver halide, eveloper and dye-forming components. When the matx is exposed in the copier, the light reaches the emulsion rrough the matrix paper stock. The emulsion in contact ith the clear areas .of the document receives the greatit amount of light. After about seconds in the activarr, these fully exposed areas are hardened so much that my adhere to the matrix and do not transfer.
While the fully exposed areas are hardened, the parally exposed areas (the document image) are dyed and zrtially developed, but not hardened. When the matrix then squeegeed and rolled in contact with Verifax opy Paper, or other suitable commercial paper, a layer the unhardened dyed material, which is still in a gelatinous state, is transferred to the copy paper. By rapidly repeating the wetting, squeegeeing and rolling, the lower layers of unhardened matrix material are successively transferred to sheets of copy paper. In this Verifax process, white areas of the copies stay white because little, if any, material is transferred to them. The image is expected to stabilize to a brown color after some time, but will remain as legible as other business papers.
The printing plates of this invention may also advantageously be employed in the Ektalith (Eastman) process. Ektalith is a trade name of Eastman Kodak Company for photocopying process and apparatus.
Broadly, the invention consists of forming an aqueous coating composition comprising a pigment, a hydrophilic colloid and a water-soluble cationic thermosetting resin.
This aqueous coating composition is then applied in a conventional manner to the surface desired, usually a wet strength paper web, and the coating dried, advantageously at a pH of about 7.0, to effect a cross-linking of the hydrophilic colloid and the water-soluble cationic thermosetting resin to form an insoluble hydrophilic planographic surface.
The type of water-soluble cationic thermosetting resins which may be employed in the practice of this invention are wet strength resins manufactured by Hercules Powder Company under the trade (name Kyrnene 557. These water-soluble cationic thermosetting resins and the methods of making them are described in detail in United States Patent No. 2,926,154.
These resins are prepared by reacting a saturated aliphatic dicarboxylic acid with a polyalkylene polyamine to form a long chain water-soluble polyamide, and then reacting the polyamide with epichlorohydrin to form a Water-soluble cationic thermosetting resin. A resin which may advantageously be employed is prepared byreacting a saturated aliphatic dicarboxylic acid containing 3 to 8 carbon atoms with from about 0.8 to about 1.4 moles, per mole of dicarboxylic acid, of a polyalkylene poly amine to form a long chain water-soluble polyamide, and then reacting the polyamide with epichlorohydrin in a mole ratio of epichlorohydrin to secondary amine groups of the polyamide of from about 0.5 to 1 to about 1.8 to l to form a water-soluble cationic thermosetting resin.
Two hundred twenty-five grams (2.18 moles) of diethylenetriamine and grams of water were placed in a S-necked flask equipped with a mechanical stirrer, thermometer and condenser. To this was added 290 grams (2.0 moles) of adipic acid. After the acid had dissolved in the amine, the solution was heated to 185-200 C. and held there for 1 hours. Then vacuum from a water pump was applied to the flask during the period required for the contents of the flask to cool to C. following which 430 grams of H 0 was added. The polyamide solution contained 52.3% solids and had an acid number of 2.1.
To 60 grams of this polyamide solution in a roundbottom flask was added 225 grams of H 0. This solution was heated to 50 C. and 12.5 grams of epichlorohydrin was added dropwise over a period of 11 minutes. The contents of the flask was then heated to 60-70 C. until it had attained a Gardner viscosity of 15. Then grams of H 0 was added to the product, and it was cooled to 25 C. Eleven ml. of 10% HCl was then added to adjust the pH to 5.0. The product contained 9.0% solids and had a Gardner viscosity of C-D.
Various pigments can be used to form the coating compositions of the printing plates of this invention such as silica, calcium silicate, barium sulfate, titanium dioxide, and clays such as kaolin, e.g. Lustra Clay. Lustra Clay is marketed by the Southern Clay Company. The pigments may be used as a mixture if desired. An example of a combined pigment which has been found to be advantageous is a mixture of about 40% by weight of colloidal silica to about 60% by weight of Lustra Clay.
planographic properties of the plates.
The colloidal silica which can be used according to this invention should contain silica particles of very small size. The main average size of the silica particles should be within a range of from about 7 millimicrons to about 30 millimicrons. Although colloidal silicas containing silica particles of less than 7 millimicrons have not been commercially available, it is believed that the coating compositions of this invention may be advantageously prepared from colloidal silicas containing silica particles of a size even less than 7 millimicrons.
The most advantageous colloidal silicas are those which contain silica particles ranging in size from about 7 to 17 millimicrons. Such colloidal silicas are marketed by E. I. du Pont de Nemoursand Company under thetradenames Ludox S.M., Ludox L.S., and Ludox HS. and
also by the Monsanto Chemical Company under the trade name Syton 200. The types of colloidal silicas and methods of making them are described in detail in United- States Patents No. 2,244,325 issued June 3, 1941, 2,574,- 902 issued November 13, l951,and 2,597,872-issued May 27, 1952.v Such colloidal silicas are generally marketed as a 30% SiO solution. but as described in the above patents the colloidal silica can be prepared containing a higher or lower percent silica.
For many purposes Ludox S.M. is desirable as this material "has a particle size of about 7 millimicrons and enables curing of the coating composition to becarried out in a shorter time. Higher machine speeds can also be used in the production of planographic plates using the Ludox S.M.
Some examples of hydrophilic colloids which can be used and reacted or cross-linked with the water-soluble cationic thermosetting resins according to this invention include amioca starch, chlorinated potato starch, polyvinyl alcohol, sodium carboxymethyl, hydroxyethyl cellulose, chlorinated corn starch, dextrin, sodium carboxymethyl cellulose, methylol polyacrylamide and polyacrylamide. The chlorinated corn starch referred to is an oxidized starch product from common corn starch by treating it in an aqueous suspension with a hypochlorite solution containing a slight excess of sodium hydroxide.
Polyvinyl alcohol has been found to be particularly advantageous.
The amounts of pigment which can be used can vary quite widely depending upon the particular hydrophilic colloid employed. We have found that a pigment-hydrophilic colloid-ratio of about 2:1 to about 7:1 is generally suitable although both higher and lower ratios can be used. When using sodium carboxymethyl cellulose as the hydrophilic colloid, we have found it to be advantageous to maintain the pigment-colloid ratio about 5:1. Depending upon the hydrophilic colloid employed, the ratio of the Kymene 557 to the colloid may advantageously be from about 30% to about The reaction or cross linking of the hydrophilic colloid with the water-soluble cationic thermosetting resin is advantageously carried out at a pH of approximately 7.0. Salts which may be advantageously used to enhance the planographic properties of the plate include zinc acetate, zinc chloride, zinc phenol sulfonate, zinc sulfamate, zinc silicofluoride, and alum, as well as salts of other divalent and tri-valent metals, e.g. lead, calcium, manganese, cerium, lanthanum. Other suitable salts can, of course, be used. The amount of salt which can be used can be varied widely depending on the particular salt employed. The amount which is utilized can be 4 readily determined by those skilled in the art.
Verifax process it is particularly advantageous to em ploy a coating composition having a pH between about 6 to 9. We have found that the pH of the coating compositions may be adjusted to the proper pH range by the use of acetic acid, ammonia, morpholine, causticsoda and the like.
The coating compositions produced according to this invention are advantageously prepared by first preparing the pigment or pigment mixture, and adding thereto the hydrophilic colloid, while stirring. Next, the watersoluble cationic thermosetting resin is added andthen the salt. The mixing may be done at room temperature and the viscosity of the mixture is advantageously adjusted to about 200 centipoises, Brookfield. The pH can be adjusted by adding ammonia or acetic acid to bring the pH to between 6 and 9 and preferably to about 7.0.
The aqueous coating compositions may be applied to a base web or sheet by conventional apparatus, suchas air knives or roll coaters. The amount of coating may vary from about 2 to 10 pounds per ream of 3300 square feet, with 6 to 8 pounds being most satisfactory. After coating, the stock is dried at normal festoon dryer temv 7' peratures (e.g. 110 F.l F.) to remove moisture. The stock is then cured by exposure to temperatures of about 325 F.350 F. for a period of 2 to 15 seconds. The curing temperature and the curing time of course will depend for example upon the type and amount of salt used, the pH of the coating composition, the particular hydrophilic colloid used, etc. -The optimum time and planographic printing plates were prepared by coating asuitable wet strength paperstock with the aqueous coating composition described therein, and drying and then curing the applied coatings by exposure to a temperature of about 325 F.-350 F. fora period of about 2-15 seconds.
Parts are by weight. 5
' Example I Eighty-four parts of a 6% sodium carboxymethyl cellulose solution were mixed with 26 parts of Lustra Clay (60% suspension) and 32 parts of Syton 200 (30% suspension), 15 parts of Kymene 557 (10% solution), 8 parts zinc acetate (25% solution), and 60 parts water. The pH of the color was adjusted to 6.5 with ammonia. The composition was coated on a paper base and then dried and cured.
Example 2 The procedure followed in Example 1 was followed except that 34 parts of a 15% solution of Penford Gum' No. 280 were used in place of the 84 parts sodium car-. boxymethyl cellulose and 30 parts of water were employed instead of 60 parts of water. Penford Gum 280 is a hydroxymethyl starch ether of a low degree of substitution -manufactured by Penick and Ford Ltd.
Example 3 Two hundred parts of an 8% solution of a high viscosity, 98% hydrolyzed polyvinyl alcohol, marketed by du Pont under the trade name Elvanol 72-51, were mixed with 83.5 parts of Lustra Clay (60% suspension) and 100 parts of Ludox S.M. (30% suspension), 48 parts higher or lower pH may be i f Kymene 557 solution), 4 parts zinc acetate (in 2 parts water) and 10 parts butyl alcohol. The pH of le color was adjusted to 9 with soda ash. The composion was coated on a paper base and then dried and cured.
Example 4 7 Example 5 Eighty nine parts of a 9% solution of a high viscosity, 3% hydrolyzed polyvinyl alcohol, marketed by du Pont ider the trade name Elvanol 72-51, were mixed with l parts of Lustra Clay (60% suspension) and 50 parts Ludox SM. (30% suspension), 5 parts of a hydrated agnesium aluminum silicate (manufactured by Attapul- 1s Minerals & Chemicals Corp. under the trade name ttasorb RVM), 24 parts of Kymene 557 (10% solution), parts zinc acetate (25% solution) and 5 parts of butyl cohol. The pH of the color was adjusted to 9 with da ash. The composition was coated on a paper base 1d then dried and cured. The cured coatings of all the printing plates produced shown in Examples 1 through 5 were hard and watersoluble, and they possessed excellent hydrophilic-01cciilic balances. These printing plates were successfully ed in the Direct Image process, the Verifax and the ttalith processes. Employing small amounts of Attarb were found to improve the tooth and image transfer the resulting plates, particularly when the plates were ed in the Verifax and the Ektalith processes. The printing plates of this invention may advantageousbe used in Xerography. Xerography is a non-chemical totographic process in which the plate is sensitized eleccally and developed by dusting with electrically charged re powder. The Xerography process is more generally scribed, for example, in United States Patent No. 2,919,- 1 issued December 29, 1959. We claim: 1. A planographic printing plate comprising a base and, hered thereto, an insolubilized coating which comprises pigment and the reaction product of a hydrophilic cold and a water-soluble cationic thermosetting resin prered by reacting a saturated aliphatic dicarboxylic acid ntaining 3 to 8 carbon atoms with from about 0.8 to out 1.4 moles, per mole of dicarboxylic acid, of a poly- :ylene polyamine having two primary amine groups dat least one secondary amine group to form a long ain water-soluble polyamide, and then reacting the polylide with epichlorohydrin in a mole ratio of epichlorodrin to secondary amine groups of the polyamide of rm about 0.5 to l to about 1.8 to l.
2. The planographic printing plate of claim 1, in which base is a paper base.
the hydrophilic colloid is polyvinyl alcohol and in which the pigment contains colloidad silica having a particle size between about 7 and millimicrons.
6. The planographic printing plate of claim 5 upon which there is placed an ink-receptive image.
7. The planographic printing plate of claim 2, in which the insolubilizecl coating contains a polyvalent metal inorganic salt.
8. The planographic printing plate of claim 1, upon which there is placed an ink-receptive image.
9. The planographic printing plate of claim 4, upon which there is placed an ink-receptive image.
10. The planographic printing plate of claim 7, upon 0 which there is placed an ink-receptive image.
11. A method of reproducing an image which comprises placing an ink-receptive image upon a planographic surface of a planographic printing plate having a paper base and a planographic coating adhered thereto comprising a pigment and the reaction product of a hydrophilic colloidand a water-soluble cationic thermosetting resin prepared by reacting a saturated aliphatic dicarboxylic acid containing 3 to 8 carbon atoms with from about 0.8 to about 1.4 moles, per mole of dicarboxylic-acid, of a polyalkylene polyamine having two primary amine groups and at least one secondary amine group to form a long chain water-soluble polyamide, and then reacting the polyamide with epichlorohydrin in a mole ratio of epichlorohydrin to secondary amine groups of the polyamide of from about 0.5 to 1 to about 1.8 to 1, contacting the planographic surface with the ink-receptive image thereon with a roll supplying an aqueous fountain solution, then contacting the planographic surface with the ink-receptive image thereon with a roll supplying greasy ink, transferring the greasy ink to a rubber blanket and transferring the ink to a copy paper.
12. The method of reproducing an image according to claim 11 in which the pigment contains a colloidal silica having a particle size between about 7 to about 30 millimicrons.
13. The method of reproducing an image according to claim 11 in which the hydrophilic colloid is polyvinyl alcohol. 4'
References Cited by the Examiner UNITED STATES PATENTS DAVID KLEIN, Primary Examiner.
ROBERT A. LEIGHEY, ROBERT E. PULFREY,
Examiners.

Claims (2)

1. A PLANOGRAPHIC PRINTING PLATE COMPRISING A BASE AND, ADHERED THERETO, AN INSOLUBILIZED COATING WHICH COMPRISES A PIGMENT AND THE REACTION PRODUCT OF A HYDROPHILIC COLLOID AND A WATER-SOLUBLE CATIONIC THERMOSETTING RESIN PREPARED BY REACTING A SATURATE ALIPHATIC DICARBOXYLIC ACID CONTAINING 3 TO 8 CARBON ATOMS WITH FROM ABOUT 0.8 TO ABOUT 1.4 MOLES, PER MOLE OF DICAROBOXYLIC ACID, OF A POLYALKYLENE POLYAMINE HAVING TWO PRIMARY AMINE GROUPS AND AT LEAST ONE SECONDARY AMINE GROUP TO FORM A LONG CHAIN WATER-SOLUBLE POLYAMIDE, AND THEN REACTING THE POLYAMIDE WITH EPICHLOROHYDRIN IN A MOLE RATIO OF EPICHLOROHYDRIN TO SECONDARY AMINE GROUPS OF THE POLYAMIDE OF FROM ABOUT 0.5 TO 1 TO ABOUT 1.8 TO 1.
8. THE PLANOGRAPHIC PRINTING PLATE OF CLAIM 1, UPON WHICH THERE IS PLACED AN INK-RECEPTIVE IMAGE.
US6839A 1960-02-05 1960-02-05 Paper offset plate for photographic transfer and direct image printing Expired - Lifetime US3181460A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US6839A US3181460A (en) 1960-02-05 1960-02-05 Paper offset plate for photographic transfer and direct image printing
GB36190/60A GB956376A (en) 1960-02-05 1960-10-21 Improvements in planographic printing plates
DEO7847A DE1216896B (en) 1960-02-05 1961-02-02 Method of making a lithographic planographic printing sheet
FR851625A FR1278588A (en) 1960-02-05 1961-02-03 Coating compositions and planographic printing plates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US6839A US3181460A (en) 1960-02-05 1960-02-05 Paper offset plate for photographic transfer and direct image printing

Publications (1)

Publication Number Publication Date
US3181460A true US3181460A (en) 1965-05-04

Family

ID=21722870

Family Applications (1)

Application Number Title Priority Date Filing Date
US6839A Expired - Lifetime US3181460A (en) 1960-02-05 1960-02-05 Paper offset plate for photographic transfer and direct image printing

Country Status (3)

Country Link
US (1) US3181460A (en)
DE (1) DE1216896B (en)
GB (1) GB956376A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3455241A (en) * 1960-11-21 1969-07-15 Oxford Paper Co Planographic printing plates
US3478716A (en) * 1963-03-07 1969-11-18 Kimberly Clark Co Printable paper product having a cellular coating containing pigment and a reaction product of protein and an epoxy resin defining the cell walls
US4046946A (en) * 1974-08-01 1977-09-06 Allied Paper Incorporated Lithographic printing plate
US4097647A (en) * 1975-11-24 1978-06-27 Allied Paper Incorporated Lithographic printing plate
US4115603A (en) * 1976-01-29 1978-09-19 Allied Paper Incorporated Process for producing lithographic printing plates having a paper base

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6105500A (en) * 1995-11-24 2000-08-22 Kodak Polychrome Graphics Llc Hydrophilized support for planographic printing plates and its preparation
GB9624224D0 (en) 1996-11-21 1997-01-08 Horsell Graphic Ind Ltd Planographic printing
GB9702568D0 (en) * 1997-02-07 1997-03-26 Horsell Graphic Ind Ltd Planographic printing
GB9710552D0 (en) 1997-05-23 1997-07-16 Horsell Graphic Ind Ltd Planographic printing
US6357351B1 (en) 1997-05-23 2002-03-19 Kodak Polychrome Graphics Llc Substrate for planographic printing
US6293197B1 (en) 1999-08-17 2001-09-25 Kodak Polychrome Graphics Hydrophilized substrate for planographic printing

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2280986A (en) * 1941-01-16 1942-04-28 Toland William Craig Coating material
US2534650A (en) * 1947-05-09 1950-12-19 Warren S D Co Planographic printing plate and method of making same
US2724665A (en) * 1953-04-17 1955-11-22 Warren S D Co Starch-coated paper-base masters for planographic printing
US2926154A (en) * 1957-09-05 1960-02-23 Hercules Powder Co Ltd Cationic thermosetting polyamide-epichlorohydrin resins and process of making same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2280986A (en) * 1941-01-16 1942-04-28 Toland William Craig Coating material
US2534650A (en) * 1947-05-09 1950-12-19 Warren S D Co Planographic printing plate and method of making same
US2724665A (en) * 1953-04-17 1955-11-22 Warren S D Co Starch-coated paper-base masters for planographic printing
US2926154A (en) * 1957-09-05 1960-02-23 Hercules Powder Co Ltd Cationic thermosetting polyamide-epichlorohydrin resins and process of making same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3455241A (en) * 1960-11-21 1969-07-15 Oxford Paper Co Planographic printing plates
US3478716A (en) * 1963-03-07 1969-11-18 Kimberly Clark Co Printable paper product having a cellular coating containing pigment and a reaction product of protein and an epoxy resin defining the cell walls
US4046946A (en) * 1974-08-01 1977-09-06 Allied Paper Incorporated Lithographic printing plate
US4097647A (en) * 1975-11-24 1978-06-27 Allied Paper Incorporated Lithographic printing plate
US4115603A (en) * 1976-01-29 1978-09-19 Allied Paper Incorporated Process for producing lithographic printing plates having a paper base

Also Published As

Publication number Publication date
DE1216896B (en) 1966-05-18
GB956376A (en) 1964-04-29

Similar Documents

Publication Publication Date Title
US3055295A (en) Planographic printing plates
US2835576A (en) Light-sensitive polyvalent metal alginate photolithographic element
US3181460A (en) Paper offset plate for photographic transfer and direct image printing
US3677178A (en) Dry planographic plates and methods, production and use
GB2155815A (en) Recording material for ink jet printing and the use thereof
US2156100A (en) Planographic printing plate and method of making the same
US2930317A (en) Planographic printing plate provided with a methylolated polyacrylamide coating and process of making
US4186250A (en) Method of desensitizing image-bearing lithographic plates
US4214531A (en) Method of treating image-bearing lithographic plates
US3507647A (en) Printing plates and method for manufacturing same
US2532866A (en) Method and plate for lithographic printing
US3922441A (en) Lithographic printing plate and method of making the same
US2794388A (en) Method of preparing a lithographic printing plate
US4200688A (en) Method of treating image-bearing lithographic plates
US3254597A (en) Planographic printing plates
US3230873A (en) Colloid coated paper with anti-wrinkling and puckering properties
US223873A (en) Process of autographic printing
US3338164A (en) Lithographic master elements for reception of hydrophobic images
US3669657A (en) Coating compositions and methods and articles
US3270667A (en) Planographic printing plates and method of making same
NO141529B (en) PROCEDURE FOR THE MANUFACTURE OF A FORM RESTORABLE OBJECT, MAINLY FOR USE AS INSULATION
US3115829A (en) Planographic printing plates
US3559579A (en) Planographic printing plates having coatings containing insoluble xanthates
JPS587396A (en) Manufacture of planographic original plate
US3368484A (en) Paper offset master