US2724665A - Starch-coated paper-base masters for planographic printing - Google Patents
Starch-coated paper-base masters for planographic printing Download PDFInfo
- Publication number
- US2724665A US2724665A US349556A US34955653A US2724665A US 2724665 A US2724665 A US 2724665A US 349556 A US349556 A US 349556A US 34955653 A US34955653 A US 34955653A US 2724665 A US2724665 A US 2724665A
- Authority
- US
- United States
- Prior art keywords
- starch
- planographic printing
- coating
- water
- hydroxyalkyl ether
- 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
Links
- 238000007639 printing Methods 0.000 title claims description 26
- 229920002472 Starch Polymers 0.000 title description 59
- 235000019698 starch Nutrition 0.000 title description 59
- 239000008107 starch Substances 0.000 title description 57
- 239000011248 coating agent Substances 0.000 claims description 24
- 238000000576 coating method Methods 0.000 claims description 24
- 239000000853 adhesive Substances 0.000 claims description 16
- 230000001070 adhesive effect Effects 0.000 claims description 16
- 239000000049 pigment Substances 0.000 claims description 16
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 7
- 239000011707 mineral Substances 0.000 claims description 7
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 239000000123 paper Substances 0.000 description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- -1 hydroxyalkyl ether Chemical compound 0.000 description 15
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
- 229920000877 Melamine resin Polymers 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000008199 coating composition Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000835 fiber Substances 0.000 description 4
- 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 4
- 229920000881 Modified starch Polymers 0.000 description 3
- 239000004368 Modified starch Substances 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 235000019426 modified starch Nutrition 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 229920001612 Hydroxyethyl starch Polymers 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 238000005903 acid hydrolysis reaction Methods 0.000 description 2
- 239000005018 casein Substances 0.000 description 2
- 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 2
- 235000021240 caseins Nutrition 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000011088 parchment paper Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229940050526 hydroxyethylstarch Drugs 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
- B41C1/00—Forme preparation
- B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
- B41C1/1091—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by physical transfer from a donor sheet having an uniform coating of lithographic material using thermal means as provided by a thermal head or a laser; by mechanical pressure, e.g. from a typewriter by electrical recording ribbon therefor
-
- 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
- B41N3/036—Chemical or electrical pretreatment characterised by the presence of a polymeric hydrophilic coating
-
- 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
- D21H19/54—Starch
-
- 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
- D21H19/62—Macromolecular organic compounds or oligomers thereof obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
Definitions
- This invention relates to the production ofcoated paperbase planographic printing masters or plates, the coating is substantially level therewith.
- the design to be repro- 1 **d is fixed on the plate surface as a water-repellent image, usually greasy, Waxy or resinous in nature.
- Water or aqueous lithographic solution is applied to the image plate and wets the unimaged areas, making them ink repellent, but does not Wet the water-repellent image.
- An inking-roll now passed over the surface leaves no ink on the water-wet background areas but does leave ink on the imaged areas which can thereafter print the image in reverse on any ink-receptive surface brought into contact therewith.
- the image is usually first printed upon an ollset blanket from which it is transferred to paper so that the final print is identical with the design of the plate.
- coated paper-base planographic printing plates or masters Such coated paper masters in general contain a hydrophilic, water-insoluble hydrophilic colloid such asspecially treated casein, a heavy metal-carbonymethylcellulose compound, or a polyvinyl alcohol which is per se insoluble in cold Water or has been rendered so by appropriate treatment as with a bichromate.
- Parchment paper e. g. paper which has been treated with strong sulfuric acid
- Parchment paper is relatively low in price and is sometimes used for masters for this purpose. Fairly satisfactory prints may be obtained therewith, but such parchment plates give a great deal of trouble because they curl quickly and badly and also tend to Wrinkle while i in use on the duplicator. Consequently, parchment paper plates, in spite of their low cost have in very large measure been replaced by more expensive coated paper plates which are easier to handle.
- the dry plate must readily accept an oleophilic image and must retain the image during the useful life of the plate.
- the imaged plate when properly wet out with aqueous lithographic solution should immediately print legible copies with a clean background, and it should continue to print at least satisfactory copies.
- the Wet plate should lie reasonably flat and it should be dimensionally stable enough so that it will not wrinkle in use.
- the plate should be relatively low in cost. It has now been found that a plate having the before enumerated minimum requirements can be produced by coating a paper web with an aqueous coating composition comprising mineral pigment, water-soluble adhesive comprising partially hydroxyalkylated starch, i. e. hydroxyalkyl ether of starch, and an insolubilizing agent for said starch adhesive. Why a water-soluble hydroxyalkylated starch should give results quite different from other available starch adhesives is not at present clear. It may be that this modified starch has somewhat better film-forming properties than starch adhesives such as oxidized starch or British gum.
- the hydroxyalkylated starch is more easily insolubilized by one of the amino-aldehyde resins which are the preferred insolubilizing agents for use according to the present invention.
- the fact is that use of the hydroxyalkylated starch as disclosed herein yields results quite different from results given by other starch adhesives in respect to planographic printing qualities.
- Partially hydroxyaikylated starch adhesives suitable for use may be produced by treatment of starch according to the disclosureof U.uS. Patents 2,516,632 or 2,516,633 of Kesler et al.
- suitable starch adhesives produced by ethylene oxide treatment of starch are the flenford gums, :so-called, sold by Penick and Ford, Ltd, inc., and considered to be hydroxyethylated starch.
- Eorshort-run coated paper planographic printing plates there is no necessity for taking steps specifically to increase the wetestrength of the paper base. "it is necessary however, that cellulose fibers from the paper base shall not project through the hydrophilic layer of coating which forms the printing surface of the plate. Severe beating or hydration of the paper-making furnish will yield a sheet free from projecting fibers, out such a sheet is liable to give trouble from curling.
- a preferable procedure is to cement down any loose or projecting fibers by means of a surface application of adhesive ma terial prior to application of the final hydrophilic coating which forms the planographic printing surface.
- a water-insoluble base-coating which may, if desired, be of composition the same as or diiferent from the subsequently applied coating which forms the hydrophilic 'planographic printing surface.
- an application of surface-size can be used to stick down the fibers, such as a starch surface-size which also contains an agent to insolubilize the starch.
- a very satisfactory surface-size for the purpose is provided by an ammoniacal solution of casein made slightly acidic by addition of formaldehyde.
- a convenient weight of paper base to use for such short-run plates is from 50 to 60 pounds per ream of 500 sheets cut 25 x 38 inches in size.
- Suitable paper may be produced from a paper-making furnish containing a mixture of chemical 'wood pulp made from both coniferous. trees. and deciduous trees, a minor quantity of clay filler, and a small proportion of rosin-size and alum.
- Such paper when surface-sized, dried, and calendered may thenbe coated with an aqueous coating composition containing mineral pigment and a lesser quantity of starch adhesive prepared from starch which has been treated with ethylene oxide to produce the planographic printing plate of the invention.
- Phosphoric acid suflicient to reduce pH to about 5.5. Water to make solids content about 40%.
- the coating to provide the hydrophilic planographic printing surface on the plate of the invention may suitably be applied in amount ranging from about 10 to 20 pounds, dry weight, per ream. Any conventional coating machine may be used for its application; an air-knife coater is very satisfactory.
- the coating material is applied in the form of an aqueous slurry containing clay or other inert mineral pigment and a lesser quantity of adhesive material comprising partially hydroxyalkylated starch such as that produced by treatment of starch with ethylene oxide according to Patent 2,516,632 or 2,516,633 before mentioned.
- An embodiment of the invention is a surface-sized sheet of the character previously described and having a basis weight of 57 pounds per ream, which carries on one side a coating amounting to 10 pounds, dry weight, per ream deposited from an aqueous coating mixture of the following composition expressed in parts by weight:
- the coated paper was force dried and supercalendered.
- the plate described can then be typed upon with a typewriter using a greasy ribbon or it can be imaged in other ways, as by a crayon, greasy pencil, or pen using an oily ink.
- the imaged plate should then be thoroughly wet by liberal application thereto of an aqueous lithographic wet-out solution carefully applied as by means of a swab of cotton or pad of molleton cloth. When once properly wet-out the plate will thereafter, when used on a rotary offset duplicator, print clean and legible copies immediately and will continue to do so for at least 500 copies.
- the quantity of ethylene oxide treated starch used in the coating composition per pound of mineral pigment will vary depending upon the particular pigment being used, the particular paper stock to which it is being applied, and the number of copies that are required to be printed from the finished plates. Obviously sufficient adhesive must be used to bind the coating to the base with sutficient force so that it willnot be pulled away from the base by the tack of the printing-ink on the press. About 25 parts of the hydroxyalkyl ether of starch per 100 parts of clay is usually considered about the minimum that can be safely used. As the quantity of the hydroxyalkyl ether of starch is increased the strength of the coating likewise increases, but tendency to trouble from curling likewise increases at the same time. Consequently about parts of the starch adhesive per parts of pigment is about the maximum ever feasible for use. Actually the preferred range will be from about 35 to 50 parts of modified starch to 100 parts'of pigment.
- the preferred way of insolubilizing the starch adhesives in manufacturing the plate of the invention is to include a significant quantity of water-soluble aminoaldehyde resin in the coating composition.
- the aminoaldehyde resin is said to be cured, and substantial water-insolubility of the coating results. It seems probable that in the curing process there is some actual reaction between the hydroxyalkyl ether of starch and the resin; otherwise the resulting insolubility of the starch would be difficult to explain.
- Most of the amino-aldehyde resins cure much more rapidly in the presence of some acidic substance which holds the pH value of the solution appreciably below 7.
- acid-catalyst is also included in the coating composition.
- water-soluble amino-aldehyde resins effective for use are dimethylol-urea, other water-soluble ureaformaldehyde condensates, and water-soluble melamineformaldehyde condensates.
- the amino-aldehyde resins in respect to time and/ or temperature required for curing.
- Naturally conditions under which the coated paper is cured or dried will be modified to suit the particular amino-aldehyde resins used to insolubilize the starch.
- melamine-formaldehyde condensates are preferred; one very satisfactory melamine-formaldehyde condensate is sold as Parez 611 by the American Cyanamid Company.
- the ratio of amino-aldehyde resin to starch may be varied considerably. Normally 25% of amino-aldehyde resin based on the weight of the hydroxyalkyl ether of starch may be expected to insolubilize the coating. If the period of curing can be prolonged, even smaller quantities of the resin may give a substantial degree of insolubility. On the other hand, considerably larger quantities of'the resin may be used if desired. In fact, a quantity of amino-aldehyde resin up to 100% of the weight of modified starch present may be included in the coating composition without making the resulting coated surface unduly sensitive or susceptible to toning.
- a weight of amino-aldehyde resin equal to about 35% of the weight of hydroxyalkylated starch present.
- melamine-resins under acidic conditions, curing of the resin results from ordinary drying of the coated paper at steam temperature for a period long enough to evaporate the water from the coating, whereas urea-resins may require more heating or a fairly long period of aging at ordinary temperature before they become cured.
- a typical water-soluble melamine-resin satisfactory for use is made by condensing 1 mole of melamine with 2 moles of formaldehyde.
- hydroxyethyl starch is at present the most easily obtainable of such starches and is very satisfactory for use.
- Hydroxyethyl starches of medium to low viscosity are preferred because they are easier to apply than starches of higher viscosity, though the latter may be used if desired.
- Very satisfactory for use is starch prepared by first treating raw starch to reduce its viscosity, as by conventional acid hydrolysis at a temperature below the gelation temperature of the starch, and then reacting the loweredviscosity starch with ethylene oxide in amount between the limits of 1% and 5% based on the dry weight of the starch.
- hydroxyalkylated starch e. g. starch treated with ethylene oxide as previously described, behaves differently and gives altogether diiferent results than do the ordinary converted starch adhesives of commerce. If, for instance, an enzyrne-converted corn starch or a starch gum such as oxidized or chlorinated starch is substituted for the Penford gum N0. 280 in the formula previously set forth, paper coated therewith will not be in any degree a useful planographic printing plate.
- a planographic printing plate comprising a paper base and a water-insoluble coating thereon presenting a planographic printing surface, said coating consisting essentially of finely divided mineral pigment and a waterinsoluble hydrophilic adhesive component comprising the reaction product of hydroxyalkyl ether of starch and an amino-aldehyde resin, the ratio of said pigment, hydroxyalkyl ether of starch and an amino-aldehyde resin being from about 25% to about 75 of the hydroxyalkyl ether of starch based upon the weight of the pigment, and from about 25% to about 100% of the amino-aldehyde resin based upon the weight of the hydroxyalkyl ether of starch.
- Process of making a planographic printing plate which comprises coating a paper base with an aqueous slurry consisting essentially of water, finely divided mineral pigment, a water-soluble hydroxyalkyl ether of starch and a Water-soluble amino-aldehyde resin, the ratio of said pigment, hydroxyalkyl ether of starch and aminoaldehyde resin being from about 25% to about of the hydroxyalkyl ether of starch based upon the weight of the pigment and from about 25% to about of the amino-aldehyde resin based upon the weight of the hydroxyalkyl ether of starch and drying and supercalendering the coated paper base under conditions capable of curing the resin.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Mechanical Engineering (AREA)
- Optics & Photonics (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Paper (AREA)
Description
United States Patent STARCH-COATED PAPER-BASE MASTERS FOR PLANOGRAPHIC PRINTING 1 Raymond L. Oransky, Portland, and Towers Doggett,
Windham, Maine, assignors to S. D. Warren Company, Boston, Mass., a corporation of Massachusetts No Drawing. Application April 17, 1953,
Serial No. 349,556
5 Claims. (Cl. 117-155) This invention relates to the production ofcoated paperbase planographic printing masters or plates, the coating is substantially level therewith. The design to be repro- 1 duced is fixed on the plate surface as a water-repellent image, usually greasy, Waxy or resinous in nature. Water or aqueous lithographic solution is applied to the image plate and wets the unimaged areas, making them ink repellent, but does not Wet the water-repellent image. An inking-roll now passed over the surface leaves no ink on the water-wet background areas but does leave ink on the imaged areas which can thereafter print the image in reverse on any ink-receptive surface brought into contact therewith. In practice the image is usually first printed upon an ollset blanket from which it is transferred to paper so that the final print is identical with the design of the plate.
In business offices it is very frequently necessary to provide from 20 to 50 copies of letters, data sheets, re-
ports and the like. At present it is generally conceded that the most satisfactory means of producing such duplicate copies is a rotary olfset duplicator. Relatively expensive metal plates can be used in such duplicators, but office personnel usually find paper-base plates easier to prepare and manipulate. There are on the market several very excellent coated paper-base planographic printing plates or masters. Such coated paper masters in general contain a hydrophilic, water-insoluble hydrophilic colloid such asspecially treated casein, a heavy metal-carbonymethylcellulose compound, or a polyvinyl alcohol which is per se insoluble in cold Water or has been rendered so by appropriate treatment as with a bichromate. Such masters, though vary considerably less costly than metal plates, are nevertheless relatively expensive to produce, so that their cost may be a considerable factor in the expense of producing small lots of duplicates, say in the order of 25. Thus, it is apparent that there is a need for a less costly master designed for use in duplicating small lots of r from to 50 copies.
Parchment paper, e. g. paper which has been treated with strong sulfuric acid, is relatively low in price and is sometimes used for masters for this purpose. Fairly satisfactory prints may be obtained therewith, but such parchment plates give a great deal of trouble because they curl quickly and badly and also tend to Wrinkle while i in use on the duplicator. Consequently, parchment paper plates, in spite of their low cost have in very large measure been replaced by more expensive coated paper plates which are easier to handle.
The minimum requirements for an acceptable shortrun coated paper planographic printing plate may be stated as follows:
1. The dry plate must readily accept an oleophilic image and must retain the image during the useful life of the plate.
2,724,665 Patented Nov. 22, 1955 2. Errors in the image must be capable of being erased with a rubber eraser, and the erased area must be capable of accepting a new image.
3. The imaged plate when properly wet out with aqueous lithographic solution should immediately print legible copies with a clean background, and it should continue to print at least satisfactory copies.
4. The Wet plate should lie reasonably flat and it should be dimensionally stable enough so that it will not wrinkle in use.
5. The plate should be relatively low in cost. It has now been found that a plate having the before enumerated minimum requirements can be produced by coating a paper web with an aqueous coating composition comprising mineral pigment, water-soluble adhesive comprising partially hydroxyalkylated starch, i. e. hydroxyalkyl ether of starch, and an insolubilizing agent for said starch adhesive. Why a water-soluble hydroxyalkylated starch should give results quite different from other available starch adhesives is not at present clear. It may be that this modified starch has somewhat better film-forming properties than starch adhesives such as oxidized starch or British gum. 0n the other hand it may be that the hydroxyalkylated starch is more easily insolubilized by one of the amino-aldehyde resins which are the preferred insolubilizing agents for use according to the present invention. Whatever the correct explanation may be, the fact is that use of the hydroxyalkylated starch as disclosed herein yields results quite different from results given by other starch adhesives in respect to planographic printing qualities.
Partially hydroxyaikylated starch adhesives suitable for use may be produced by treatment of starch according to the disclosureof U.uS. Patents 2,516,632 or 2,516,633 of Kesler et al. Examples of suitable starch adhesives produced by ethylene oxide treatment of starch are the flenford gums, :so-called, sold by Penick and Ford, Ltd, inc., and considered to be hydroxyethylated starch.
Eorshort-run coated paper planographic printing plates there is no necessity for taking steps specifically to increase the wetestrength of the paper base. "it is necessary however, that cellulose fibers from the paper base shall not project through the hydrophilic layer of coating which forms the printing surface of the plate. Severe beating or hydration of the paper-making furnish will yield a sheet free from projecting fibers, out such a sheet is liable to give trouble from curling. Hence, a preferable procedure is to cement down any loose or projecting fibers by means of a surface application of adhesive ma terial prior to application of the final hydrophilic coating which forms the planographic printing surface.
There may be used to cover over and stick down projecting fibers a water-insoluble base-coating which may, if desired, be of composition the same as or diiferent from the subsequently applied coating which forms the hydrophilic 'planographic printing surface. 01' if desired, an application of surface-size can be used to stick down the fibers, such as a starch surface-size which also contains an agent to insolubilize the starch. A very satisfactory surface-size for the purpose is provided by an ammoniacal solution of casein made slightly acidic by addition of formaldehyde.
A convenient weight of paper base to use for such short-run plates is from 50 to 60 pounds per ream of 500 sheets cut 25 x 38 inches in size. Suitable paper may be produced from a paper-making furnish containing a mixture of chemical 'wood pulp made from both coniferous. trees. and deciduous trees, a minor quantity of clay filler, and a small proportion of rosin-size and alum. Such paper when surface-sized, dried, and calendered may thenbe coated with an aqueous coating composition containing mineral pigment and a lesser quantity of starch adhesive prepared from starch which has been treated with ethylene oxide to produce the planographic printing plate of the invention.
Since only one side of a printing plate is used for reproduction, from the viewpoint, solely of printing it is not necessary to give any treatment to the reverse side of the paper base. As a practical matter, however, in order to minimize any tendency of the sheet to curl and in general to give better stability to the sheet it is desirable to apply a coating of some kind to the reverse side of the paper base. It is likewise advisable to use for this purpose a coating which is relatively water-insoluble so that if in use it inadvertently becomes wetted it will not stick to the plate cylinder by which it may be supported in a printing press. The exact composition of the backcoating is of little'importance. A very satisfactory coating is about pounds, dry weight per ream, of the following compositions:
Phosphoric acid suflicient to reduce pH to about 5.5. Water to make solids content about 40%.
The coating to provide the hydrophilic planographic printing surface on the plate of the invention may suitably be applied in amount ranging from about 10 to 20 pounds, dry weight, per ream. Any conventional coating machine may be used for its application; an air-knife coater is very satisfactory. The coating material is applied in the form of an aqueous slurry containing clay or other inert mineral pigment and a lesser quantity of adhesive material comprising partially hydroxyalkylated starch such as that produced by treatment of starch with ethylene oxide according to Patent 2,516,632 or 2,516,633 before mentioned.
An embodiment of the invention is a surface-sized sheet of the character previously described and having a basis weight of 57 pounds per ream, which carries on one side a coating amounting to 10 pounds, dry weight, per ream deposited from an aqueous coating mixture of the following composition expressed in parts by weight:
Water to make solids content about 26%.
The coated paper was force dried and supercalendered. The plate described can then be typed upon with a typewriter using a greasy ribbon or it can be imaged in other ways, as by a crayon, greasy pencil, or pen using an oily ink. The imaged plate should then be thoroughly wet by liberal application thereto of an aqueous lithographic wet-out solution carefully applied as by means of a swab of cotton or pad of molleton cloth. When once properly wet-out the plate will thereafter, when used on a rotary offset duplicator, print clean and legible copies immediately and will continue to do so for at least 500 copies.
The quantity of ethylene oxide treated starch used in the coating composition per pound of mineral pigment will vary depending upon the particular pigment being used, the particular paper stock to which it is being applied, and the number of copies that are required to be printed from the finished plates. Obviously sufficient adhesive must be used to bind the coating to the base with sutficient force so that it willnot be pulled away from the base by the tack of the printing-ink on the press. About 25 parts of the hydroxyalkyl ether of starch per 100 parts of clay is usually considered about the minimum that can be safely used. As the quantity of the hydroxyalkyl ether of starch is increased the strength of the coating likewise increases, but tendency to trouble from curling likewise increases at the same time. Consequently about parts of the starch adhesive per parts of pigment is about the maximum ever feasible for use. Actually the preferred range will be from about 35 to 50 parts of modified starch to 100 parts'of pigment.
The preferred way of insolubilizing the starch adhesives in manufacturing the plate of the invention is to include a significant quantity of water-soluble aminoaldehyde resin in the coating composition. When the mixture is subjected to force-drying with heat the aminoaldehyde resin is said to be cured, and substantial water-insolubility of the coating results. It seems probable that in the curing process there is some actual reaction between the hydroxyalkyl ether of starch and the resin; otherwise the resulting insolubility of the starch would be difficult to explain. Most of the amino-aldehyde resins cure much more rapidly in the presence of some acidic substance which holds the pH value of the solution appreciably below 7. When using such an acidcuring resin in making the plate of the invention,'a socalled acid-catalyst is also included in the coating composition.
Among the water-soluble amino-aldehyde resins effective for use are dimethylol-urea, other water-soluble ureaformaldehyde condensates, and water-soluble melamineformaldehyde condensates. There are some differences among the amino-aldehyde resins in respect to time and/ or temperature required for curing. Naturally conditions under which the coated paper is cured or dried will be modified to suit the particular amino-aldehyde resins used to insolubilize the starch. In general, melamine-formaldehyde condensates are preferred; one very satisfactory melamine-formaldehyde condensate is sold as Parez 611 by the American Cyanamid Company.
The ratio of amino-aldehyde resin to starch may be varied considerably. Normally 25% of amino-aldehyde resin based on the weight of the hydroxyalkyl ether of starch may be expected to insolubilize the coating. If the period of curing can be prolonged, even smaller quantities of the resin may give a substantial degree of insolubility. On the other hand, considerably larger quantities of'the resin may be used if desired. In fact, a quantity of amino-aldehyde resin up to 100% of the weight of modified starch present may be included in the coating composition without making the resulting coated surface unduly sensitive or susceptible to toning. In everyday operation it is convenient to use a weight of amino-aldehyde resin equal to about 35% of the weight of hydroxyalkylated starch present. When melamine-resins are used, under acidic conditions, curing of the resin results from ordinary drying of the coated paper at steam temperature for a period long enough to evaporate the water from the coating, whereas urea-resins may require more heating or a fairly long period of aging at ordinary temperature before they become cured. A typical water-soluble melamine-resin satisfactory for use is made by condensing 1 mole of melamine with 2 moles of formaldehyde.
While any water-soluble hydroxyalkylated starch will give improved results according to the invention, hydroxyethyl starch is at present the most easily obtainable of such starches and is very satisfactory for use. Hydroxyethyl starches of medium to low viscosity are preferred because they are easier to apply than starches of higher viscosity, though the latter may be used if desired. Very satisfactory for use is starch prepared by first treating raw starch to reduce its viscosity, as by conventional acid hydrolysis at a temperature below the gelation temperature of the starch, and then reacting the loweredviscosity starch with ethylene oxide in amount between the limits of 1% and 5% based on the dry weight of the starch.
Insofar as planographic printing is concerned hydroxyalkylated starch, e. g. starch treated with ethylene oxide as previously described, behaves differently and gives altogether diiferent results than do the ordinary converted starch adhesives of commerce. If, for instance, an enzyrne-converted corn starch or a starch gum such as oxidized or chlorinated starch is substituted for the Penford gum N0. 280 in the formula previously set forth, paper coated therewith will not be in any degree a useful planographic printing plate. For if an attempt ismade to print from such a product on an offset printing press, either the background will accept ink and so print black all over, or if a huge excess of aqueous fountain-solution is used to keep the background clean the image will be obliterated. In either case the plate is utterly useless. With use of hydroxyalkylated starch in the formula, how ever, the coated product serves excellently as a planographic printing plate, immediately yielding prints with clean background and distinct images and continuously producing them for 100 copies or more.
We claim:
1. A planographic printing plate comprising a paper base and a water-insoluble coating thereon presenting a planographic printing surface, said coating consisting essentially of finely divided mineral pigment and a waterinsoluble hydrophilic adhesive component comprising the reaction product of hydroxyalkyl ether of starch and an amino-aldehyde resin, the ratio of said pigment, hydroxyalkyl ether of starch and an amino-aldehyde resin being from about 25% to about 75 of the hydroxyalkyl ether of starch based upon the weight of the pigment, and from about 25% to about 100% of the amino-aldehyde resin based upon the weight of the hydroxyalkyl ether of starch.
2. A planographic printing plate according to claim 1 in which the hydroxyalkyl ether of starch is a hydroxyethyl ether of starch.
3. A planographic printing plate as defined in claim 1 in which the amino-aldehyde resin is a melamine-formaldehyde condensate.
4. Process of making a planographic printing plate which comprises coating a paper base with an aqueous slurry consisting essentially of water, finely divided mineral pigment, a water-soluble hydroxyalkyl ether of starch and a Water-soluble amino-aldehyde resin, the ratio of said pigment, hydroxyalkyl ether of starch and aminoaldehyde resin being from about 25% to about of the hydroxyalkyl ether of starch based upon the weight of the pigment and from about 25% to about of the amino-aldehyde resin based upon the weight of the hydroxyalkyl ether of starch and drying and supercalendering the coated paper base under conditions capable of curing the resin.
5. A planographic printing plate as defined in claim 1 in which the hydroxyalkyl ether of starch is the product obtained by subjecting starch to acid hydrolysis at a temperature below its gelation temperature to reduce its viscosity and then reacting it with from 1% to 5% of ethylene oxide based upon the dry weight of the starch.
References Cited in the file of this patent UNITED STATES PATENTS
Claims (1)
1. A PLANOGRAPHIC PRINTING PLATE COMPRISING A PAPER BASE AND A WATER-INSOLUBLE COATING THEREON PRESENTING A PLANOGRAPHIC PRINTING SURFACE, SAID COATING CONSISTING ESSENTIALLY OF FINELY DIVIDED MINERAL PIGMENT AND A WATERINSOLUBLE HYDROPHILIC ADHESIVE COMPONENT COMPRISING THE REACTION PRODUCT OF HYDROXYALKYL ETHER OF STARCH AND AN AMINO-ALDEHYDE RESIN, THE RATIO OF SAID PIGMENT, HYDROXYALKYL ETHER OF STARCH AND AN AMINO-ALDEHYDE RESIN BEING FROM ABOUT 25% TO ABOUT 75% OF THE HYDROXYALKYL ETHER OF STARCH BASED UPON THE WEIGHT OF THE PIGMENT, AND FROM ABOUT 25% TO ABOUT 100% OF THEAMINO-ALDEHYDE RESIN BASED UPON THE WEIGHT OF THE HYDROXYALKYL ETHER OF STARCH.
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL200213D NL200213A (en) | 1953-04-17 | ||
| BE541312D BE541312A (en) | 1953-04-17 | ||
| NL96268D NL96268C (en) | 1953-04-17 | ||
| US349556A US2724665A (en) | 1953-04-17 | 1953-04-17 | Starch-coated paper-base masters for planographic printing |
| GB233954A GB746226A (en) | 1953-04-17 | 1954-01-26 | Starch-coated paper-base masters for planographic printing |
| US51900555 US2876134A (en) | 1953-04-17 | 1955-06-29 | Starch-coated paper-base masters for planographic printing |
| DEW17466A DE1032761B (en) | 1953-04-17 | 1955-09-10 | Process for the production of a planographic printing film with a paper backing |
| FR1136013D FR1136013A (en) | 1953-04-17 | 1955-09-13 | Paper-based cliché, covered with starch for planographic printing |
| GB1658156A GB788282A (en) | 1953-04-17 | 1956-05-29 | Starch coated paper-base masters for planographic printing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US349556A US2724665A (en) | 1953-04-17 | 1953-04-17 | Starch-coated paper-base masters for planographic printing |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2724665A true US2724665A (en) | 1955-11-22 |
Family
ID=23372900
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US349556A Expired - Lifetime US2724665A (en) | 1953-04-17 | 1953-04-17 | Starch-coated paper-base masters for planographic printing |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2724665A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2778301A (en) * | 1953-05-22 | 1957-01-22 | Warren S D Co | Coated paper planographic printing plate |
| US2805621A (en) * | 1954-02-10 | 1957-09-10 | Standard Register Co | Paper planographic plate |
| US2876134A (en) * | 1953-04-17 | 1959-03-03 | Raymond L Oransky | Starch-coated paper-base masters for planographic printing |
| US2930317A (en) * | 1956-12-19 | 1960-03-29 | Oxford Paper Co | Planographic printing plate provided with a methylolated polyacrylamide coating and process of making |
| US3016823A (en) * | 1958-06-11 | 1962-01-16 | Fitchburg Paper | Lithographic printing plate and method of making the same |
| US3017827A (en) * | 1957-08-29 | 1962-01-23 | Oxford Paper Co | Aqueous coating composition comprising water soluble polyethylenepolyamine-dihaloalkane urea-formaldehyde reactiion product and planographic paper base formed with same |
| US3047392A (en) * | 1960-02-01 | 1962-07-31 | Honeywell Regulator Co | Photographic hydroxyethyl starch silver halide print-out composition |
| US3131630A (en) * | 1959-06-08 | 1964-05-05 | Gestetner Ltd | Planographic printing plates |
| US3181460A (en) * | 1960-02-05 | 1965-05-04 | Oxford Paper Co | Paper offset plate for photographic transfer and direct image printing |
| DE1193521B (en) * | 1956-09-18 | 1965-05-26 | Oxford Paper Company | Lithographic planographic printing film and process for its manufacture |
| US3308009A (en) * | 1963-12-16 | 1967-03-07 | Jr George L Baumgartner | Curl-resistant vinyl cork tile |
| US3778263A (en) * | 1968-06-14 | 1973-12-11 | Ricoh Kk | Zinc oxide photoconductive element with starch reaction product interlayer |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2297698A (en) * | 1940-07-20 | 1942-10-06 | Dow Chemical Co | Treating bibulous paper |
| US2622997A (en) * | 1947-05-30 | 1952-12-23 | Scholten Chemische Fab | Process of producing insoluble coating from salts of carboxylic acids |
-
1953
- 1953-04-17 US US349556A patent/US2724665A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2297698A (en) * | 1940-07-20 | 1942-10-06 | Dow Chemical Co | Treating bibulous paper |
| US2622997A (en) * | 1947-05-30 | 1952-12-23 | Scholten Chemische Fab | Process of producing insoluble coating from salts of carboxylic acids |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2876134A (en) * | 1953-04-17 | 1959-03-03 | Raymond L Oransky | Starch-coated paper-base masters for planographic printing |
| US2778301A (en) * | 1953-05-22 | 1957-01-22 | Warren S D Co | Coated paper planographic printing plate |
| US2805621A (en) * | 1954-02-10 | 1957-09-10 | Standard Register Co | Paper planographic plate |
| DE1193521B (en) * | 1956-09-18 | 1965-05-26 | Oxford Paper Company | Lithographic planographic printing film and process for its manufacture |
| US2930317A (en) * | 1956-12-19 | 1960-03-29 | Oxford Paper Co | Planographic printing plate provided with a methylolated polyacrylamide coating and process of making |
| US3017827A (en) * | 1957-08-29 | 1962-01-23 | Oxford Paper Co | Aqueous coating composition comprising water soluble polyethylenepolyamine-dihaloalkane urea-formaldehyde reactiion product and planographic paper base formed with same |
| US3016823A (en) * | 1958-06-11 | 1962-01-16 | Fitchburg Paper | Lithographic printing plate and method of making the same |
| US3131630A (en) * | 1959-06-08 | 1964-05-05 | Gestetner Ltd | Planographic printing plates |
| US3047392A (en) * | 1960-02-01 | 1962-07-31 | Honeywell Regulator Co | Photographic hydroxyethyl starch silver halide print-out composition |
| US3181460A (en) * | 1960-02-05 | 1965-05-04 | Oxford Paper Co | Paper offset plate for photographic transfer and direct image printing |
| US3308009A (en) * | 1963-12-16 | 1967-03-07 | Jr George L Baumgartner | Curl-resistant vinyl cork tile |
| US3778263A (en) * | 1968-06-14 | 1973-12-11 | Ricoh Kk | Zinc oxide photoconductive element with starch reaction product interlayer |
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