CA2242561C - Offset lithographic printing process - Google Patents
Offset lithographic printing process Download PDFInfo
- Publication number
- CA2242561C CA2242561C CA002242561A CA2242561A CA2242561C CA 2242561 C CA2242561 C CA 2242561C CA 002242561 A CA002242561 A CA 002242561A CA 2242561 A CA2242561 A CA 2242561A CA 2242561 C CA2242561 C CA 2242561C
- Authority
- CA
- Canada
- Prior art keywords
- pigment
- ink
- present
- water
- macromolecular
- 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 - Fee Related
Links
- 238000007639 printing Methods 0.000 title claims abstract description 68
- 238000000034 method Methods 0.000 title claims abstract description 57
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000000049 pigment Substances 0.000 claims abstract description 24
- 239000011230 binding agent Substances 0.000 claims abstract description 23
- 239000000839 emulsion Substances 0.000 claims abstract description 5
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 4
- 239000000080 wetting agent Substances 0.000 claims abstract description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 6
- HBAIZGPCSAAFSU-UHFFFAOYSA-N 1-(2-hydroxyethyl)imidazolidin-2-one Chemical compound OCCN1CCNC1=O HBAIZGPCSAAFSU-UHFFFAOYSA-N 0.000 claims description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 4
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 125000005396 acrylic acid ester group Chemical group 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 150000002334 glycols Chemical class 0.000 claims description 4
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 4
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 4
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 4
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 2
- RPZANUYHRMRTTE-UHFFFAOYSA-N 2,3,4-trimethoxy-6-(methoxymethyl)-5-[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxyoxane;1-[[3,4,5-tris(2-hydroxybutoxy)-6-[4,5,6-tris(2-hydroxybutoxy)-2-(2-hydroxybutoxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]butan-2-ol Chemical compound COC1C(OC)C(OC)C(COC)OC1OC1C(OC)C(OC)C(OC)OC1COC.CCC(O)COC1C(OCC(O)CC)C(OCC(O)CC)C(COCC(O)CC)OC1OC1C(OCC(O)CC)C(OCC(O)CC)C(OCC(O)CC)OC1COCC(O)CC RPZANUYHRMRTTE-UHFFFAOYSA-N 0.000 claims description 2
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 claims description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 2
- 239000004908 Emulsion polymer Substances 0.000 claims description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- 229920002873 Polyethylenimine Polymers 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- 235000012544 Viola sororia Nutrition 0.000 claims description 2
- 241001106476 Violaceae Species 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 2
- 239000012530 fluid Substances 0.000 claims description 2
- 235000021384 green leafy vegetables Nutrition 0.000 claims description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 2
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- 229920002401 polyacrylamide Polymers 0.000 claims description 2
- 239000011118 polyvinyl acetate Substances 0.000 claims description 2
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 239000000600 sorbitol Substances 0.000 claims description 2
- 150000005846 sugar alcohols Polymers 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 239000000976 ink Substances 0.000 description 54
- 239000012855 volatile organic compound Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 230000002209 hydrophobic effect Effects 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- 238000007646 gravure printing Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000007246 mechanism Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 229940071676 hydroxypropylcellulose Drugs 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- -1 Polyethylene Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 229940105329 carboxymethylcellulose Drugs 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229940005642 polystyrene sulfonic acid Drugs 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M1/00—Inking and printing with a printer's forme
- B41M1/06—Lithographic printing
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
An offset lithographic printing process utilizing a water-based printing ink.
The process is conducted at a relative humidity of 75-100 % and preferably at a temperature of 10-30 °C. A useful water-based ink comprises water; a macromolecular binder which: (i) is optionally present and is of the type which is water-soluble, regardless of the pH of the water phase, (ii) is present and is of the type which is water-soluble only at a pre-determined pH value, or (iii) is optionally present and is an aqueous emulsion; a pigment; and a re-wetting agent. A nonionic surfactant may also be present in the ink.
The process is conducted at a relative humidity of 75-100 % and preferably at a temperature of 10-30 °C. A useful water-based ink comprises water; a macromolecular binder which: (i) is optionally present and is of the type which is water-soluble, regardless of the pH of the water phase, (ii) is present and is of the type which is water-soluble only at a pre-determined pH value, or (iii) is optionally present and is an aqueous emulsion; a pigment; and a re-wetting agent. A nonionic surfactant may also be present in the ink.
Description
OFFSET LITHOGRAPHIC PRINTING PROCESS
FIELD OF THE INVENTION
The invention relates to an offset lithographic printing process utilizing a water-based ink composition.
The process is conducted out at a relative humidity of 75-100% and preferably at a temperature of 10 to 30 C.
The ink composition will typically contain water, one or more macromolecular binders, a pigment and a re-wetting agent.
BACKGROUND OF THE INVENTION
In an attempt to eliminate VOC's in the pressroom, water-based alternatives are being sought for ink formulations. Water-based printing inks for use in flexographic printing processes are known in the prior art. This type of printing process utilizes printing plates wherein the printing images stand up in relief, i.e. the areas to be printed are raised above the non-printing areas. Printing by the flexographic procesr requires relatively low pressure - sufficient pressure is applied to transfer the ink from the face of the image carrier to the surface of the substrate. Examples of useful water-based flexographic printing inks are disclosed in US Patent 4,173,554 and The Printinq Ink Manual, edited by R.H. Leach and R.J. Pierce, pages 571-576, 5th edition, (Blueprint, 1993).
Water-based inks for gravure printing are also well known. In the gravure process, the printing image is engraved into a cylinder in the form of cells which become filled with ink. Printing is achieved by passing the substrate between the gravure cylinder and impression roller under pressure. Examples of useful water-based gravure printing inks are disclosed in US Patents 4,954,556 and 5,098,478.
The offset lithographic printing process presents unique challenges to ink formulators since such process utilizes a planographic printing plate, i.e. the image and non-image areas are in the same plane on the image carrier, and two fluids are concurrently utilized.
It is fairly simple to define an image area by raising it above the background as iri the case of the flexographic printing plate or lowering it as in the case of the gravure printing plate; avoidance of ink adhering to the non-image area is not too difficult to achieve.
However, when all areas are on the same level, techniques must be utilized to insure that ink adheres only to the image area, and not to the non-image area.
In conventional offset lithographic printing processes, the plate is damped before it is inked with an oil-based ink. Typically, the damping process utilizes a fountain solution such as those described in US patents 3,877,372, 4,278,467 and 4,854,969. Water will form a film on the hydrophilic areas (i.e. the non-image areas) of the printing plate, but will contract into tiny droplets on the oleophilic areas (i.e. the image areas).
When an inked roller containing the oil-based ink is passed over the damped plate, it will be unable to ink the areas covered by the water film (the non-image areas), but will emulsify the droplets on the water-repellant areas (the image areas) and these will ink up.
Such process is called offset lithography because the inked image on the plate does not directly print onto the paper substrate, but is first "offset" onto a rubber blanket, and transferred therefrom onto the paper substrate.
WO 97/33757 PCTlUS97/03868 As mentioned above, conventional offset lithographic printing processes entails the use of oil-based inks and water-based fountain solutions. The ink/water balance is critical and is quite demanding of the pressman's skills.
This issue is one of the several disadvantages associated with such printing processes as compared to flexographic and gravure printing processes. Moreover, the oil-based inks and aqueous fountain solutions typically employed in conventional offset lithographic printing processes contain fairly high levels of undesirable volatile organic compounds ("VOCs").
U.S. Patent 3,356,030 discloses the use of a water-based printing ink in respect to a method of planographic printing utilizing a lithographic printing plate whose non-image areas are coated with a cured coating of a thermosetting silicone resin. However, the patented method also entails the use of a volatile hydrocarbon fountain solution which will coat the non-image areas and which is re-applied between successive printings. Of course, the use of a volatile hydrocarbon fountain solution undermines the principal purpose of the offset lithographic printing process of the present invention, i.e. the avoidance of the use of volatile organic compounds ("VOCs") during the printing process. Indeed, the offset lithographic printing process utilizes water-based ink compositions without any fountain solution whatsoever.
In the 1980s, a resurgence of interest occurred in respect to "waterless" lithographic printing processes.
Both positive and negative waterless planographic printing plates are commercially available from Toray Industries of Japan. The image area of a waterless planographic plate is a photopolymer similar to that employed for the image area of a conventional plate.
FIELD OF THE INVENTION
The invention relates to an offset lithographic printing process utilizing a water-based ink composition.
The process is conducted out at a relative humidity of 75-100% and preferably at a temperature of 10 to 30 C.
The ink composition will typically contain water, one or more macromolecular binders, a pigment and a re-wetting agent.
BACKGROUND OF THE INVENTION
In an attempt to eliminate VOC's in the pressroom, water-based alternatives are being sought for ink formulations. Water-based printing inks for use in flexographic printing processes are known in the prior art. This type of printing process utilizes printing plates wherein the printing images stand up in relief, i.e. the areas to be printed are raised above the non-printing areas. Printing by the flexographic procesr requires relatively low pressure - sufficient pressure is applied to transfer the ink from the face of the image carrier to the surface of the substrate. Examples of useful water-based flexographic printing inks are disclosed in US Patent 4,173,554 and The Printinq Ink Manual, edited by R.H. Leach and R.J. Pierce, pages 571-576, 5th edition, (Blueprint, 1993).
Water-based inks for gravure printing are also well known. In the gravure process, the printing image is engraved into a cylinder in the form of cells which become filled with ink. Printing is achieved by passing the substrate between the gravure cylinder and impression roller under pressure. Examples of useful water-based gravure printing inks are disclosed in US Patents 4,954,556 and 5,098,478.
The offset lithographic printing process presents unique challenges to ink formulators since such process utilizes a planographic printing plate, i.e. the image and non-image areas are in the same plane on the image carrier, and two fluids are concurrently utilized.
It is fairly simple to define an image area by raising it above the background as iri the case of the flexographic printing plate or lowering it as in the case of the gravure printing plate; avoidance of ink adhering to the non-image area is not too difficult to achieve.
However, when all areas are on the same level, techniques must be utilized to insure that ink adheres only to the image area, and not to the non-image area.
In conventional offset lithographic printing processes, the plate is damped before it is inked with an oil-based ink. Typically, the damping process utilizes a fountain solution such as those described in US patents 3,877,372, 4,278,467 and 4,854,969. Water will form a film on the hydrophilic areas (i.e. the non-image areas) of the printing plate, but will contract into tiny droplets on the oleophilic areas (i.e. the image areas).
When an inked roller containing the oil-based ink is passed over the damped plate, it will be unable to ink the areas covered by the water film (the non-image areas), but will emulsify the droplets on the water-repellant areas (the image areas) and these will ink up.
Such process is called offset lithography because the inked image on the plate does not directly print onto the paper substrate, but is first "offset" onto a rubber blanket, and transferred therefrom onto the paper substrate.
WO 97/33757 PCTlUS97/03868 As mentioned above, conventional offset lithographic printing processes entails the use of oil-based inks and water-based fountain solutions. The ink/water balance is critical and is quite demanding of the pressman's skills.
This issue is one of the several disadvantages associated with such printing processes as compared to flexographic and gravure printing processes. Moreover, the oil-based inks and aqueous fountain solutions typically employed in conventional offset lithographic printing processes contain fairly high levels of undesirable volatile organic compounds ("VOCs").
U.S. Patent 3,356,030 discloses the use of a water-based printing ink in respect to a method of planographic printing utilizing a lithographic printing plate whose non-image areas are coated with a cured coating of a thermosetting silicone resin. However, the patented method also entails the use of a volatile hydrocarbon fountain solution which will coat the non-image areas and which is re-applied between successive printings. Of course, the use of a volatile hydrocarbon fountain solution undermines the principal purpose of the offset lithographic printing process of the present invention, i.e. the avoidance of the use of volatile organic compounds ("VOCs") during the printing process. Indeed, the offset lithographic printing process utilizes water-based ink compositions without any fountain solution whatsoever.
In the 1980s, a resurgence of interest occurred in respect to "waterless" lithographic printing processes.
Both positive and negative waterless planographic printing plates are commercially available from Toray Industries of Japan. The image area of a waterless planographic plate is a photopolymer similar to that employed for the image area of a conventional plate.
However, the non-iiaage area is coated with a polymer such as a silicone which is ink repellent. Further information about waterless printing plates and processes may be found in U.S. Patents 5,370,906 and 5,417,749.
The waterless printing process solved two issues: VOCs emanating from the fountain solutions and control of the ink/water balance :by the pressman. However, the difference in surface energy between the image and non-image areas of the conventional offset lithographic printing plate is typically 4 x 10-4 N/cm (40 dynes/cm), and is dramatically reduced to 2 x 10-4 N/cm (20 dynes/cm) in the case of the waterless printing plate. Therefore, the latitude between scumming and poor print density is considerably narrowed and the issue of VOCs (emanating from the oil-based ink) still remains in respect of waterless printing.
German Offenlegungsschrift DE 41 19 348 Al pertains to a moistureless offset printing method and a water-based printing ink. The ink described therein is one which will adhere to hydrophilic materials, but not to hydrophobic materials, and contains a dye, water, 5-50%
water-soluble macromolecular binder and a hygroscopic liquid, preferably a multihydric alcohol.
OBJECT OF THE INVENTION
It is an object of the present invention to eliminate the principal disadvantages of conventional offset lithographic printing processes, viz. high levels of VOCs emanating from the oil-based ink and the aqueous fountain solution and the difficulty in controlling the ink/water balance, while preserving the principal advantage of the offset lithographic printing process, i.e., high surface energy differential between the image and non-image areas of the printing plate.
The waterless printing process solved two issues: VOCs emanating from the fountain solutions and control of the ink/water balance :by the pressman. However, the difference in surface energy between the image and non-image areas of the conventional offset lithographic printing plate is typically 4 x 10-4 N/cm (40 dynes/cm), and is dramatically reduced to 2 x 10-4 N/cm (20 dynes/cm) in the case of the waterless printing plate. Therefore, the latitude between scumming and poor print density is considerably narrowed and the issue of VOCs (emanating from the oil-based ink) still remains in respect of waterless printing.
German Offenlegungsschrift DE 41 19 348 Al pertains to a moistureless offset printing method and a water-based printing ink. The ink described therein is one which will adhere to hydrophilic materials, but not to hydrophobic materials, and contains a dye, water, 5-50%
water-soluble macromolecular binder and a hygroscopic liquid, preferably a multihydric alcohol.
OBJECT OF THE INVENTION
It is an object of the present invention to eliminate the principal disadvantages of conventional offset lithographic printing processes, viz. high levels of VOCs emanating from the oil-based ink and the aqueous fountain solution and the difficulty in controlling the ink/water balance, while preserving the principal advantage of the offset lithographic printing process, i.e., high surface energy differential between the image and non-image areas of the printing plate.
Such object-has been achieved by means of the offset lithographic printing process of the invention.
DETAILED DESCRIPTION OF THE INVENTION
The offset lithographic printing process of the invention is conducted at a relative humidity of 75-100*, preferably 80-85%. Desirably, the process is conducted at a temperature of 10 to 30 C, preferably 15 to 25 C.
The process will utilize a water-based printing ink without the need for any accompanying fountain solution.
5 The water-based ink for the offset lithographic printing process of the invention may be one which contains water, one or more macromolecular binders, a pigment and a rewetting agent.
The printing plates for use with the offset lithographic printing process of the invention should be such that the image areas thereof are hydrophilic in nature, while the non-image areas are hydrophobic in nature. An example of a suitable printing plate is the "waterless" Toray type discussed above. However, the image area of the plate need not contain a photopolymer.
The image area of the plate may comprise, e.g. a grained aluminum surface which has no coating thereon, but is hydrophilic in nature. The non-image area of the plate must, of course, be hydrophobic in nature. However, the non-image area may be covered with any type of hydrophobic material, provided that such hydrophobic material adheres to the non-images area of the plate during the printing process.
DETAILED DESCRIPTION OF THE INVENTION
The offset lithographic printing process of the invention is conducted at a relative humidity of 75-100*, preferably 80-85%. Desirably, the process is conducted at a temperature of 10 to 30 C, preferably 15 to 25 C.
The process will utilize a water-based printing ink without the need for any accompanying fountain solution.
5 The water-based ink for the offset lithographic printing process of the invention may be one which contains water, one or more macromolecular binders, a pigment and a rewetting agent.
The printing plates for use with the offset lithographic printing process of the invention should be such that the image areas thereof are hydrophilic in nature, while the non-image areas are hydrophobic in nature. An example of a suitable printing plate is the "waterless" Toray type discussed above. However, the image area of the plate need not contain a photopolymer.
The image area of the plate may comprise, e.g. a grained aluminum surface which has no coating thereon, but is hydrophilic in nature. The non-image area of the plate must, of course, be hydrophobic in nature. However, the non-image area may be covered with any type of hydrophobic material, provided that such hydrophobic material adheres to the non-images area of the plate during the printing process.
A useful water-based printing ink for the offset lithographic printing process of the invention may comprise the following components:
(a) 25 to 60 wtA, preferably 35 to 50 wtA, based on the weight of the ink, of water which is present as a continuous phase in the ink;
(b) 10 to 70 wtA, preferably 30 to 60 wtA, based on the weight of the ink, of a macromolecular binder comprising:
(i) macromolecular binders which are soluble in the water phase regardless of the pH of the water phase, present in an amount of 0-5 wtA, based on the weight of the ink;
and (ii) macromolecular binders which are soluble in the water phase only at a pre-determined pH value (preferably in the range of about 7.5 to about 10), present in an amount of 10-70 wtA, based on the weight of the ink; and (iii) macromoZecular binders comprising aqueous emulsions, present in an amount of 0-20 wt.%, based on the weight of the ink;
(c) a pigment, present in the amount of 2-30 wtA, preferably 5-20 wtA, based on the weight of the ink; and (d) a re-wetting agent, present in the amount of 0.5-10 wtA, based on the weight of the ink.
(a) 25 to 60 wtA, preferably 35 to 50 wtA, based on the weight of the ink, of water which is present as a continuous phase in the ink;
(b) 10 to 70 wtA, preferably 30 to 60 wtA, based on the weight of the ink, of a macromolecular binder comprising:
(i) macromolecular binders which are soluble in the water phase regardless of the pH of the water phase, present in an amount of 0-5 wtA, based on the weight of the ink;
and (ii) macromolecular binders which are soluble in the water phase only at a pre-determined pH value (preferably in the range of about 7.5 to about 10), present in an amount of 10-70 wtA, based on the weight of the ink; and (iii) macromoZecular binders comprising aqueous emulsions, present in an amount of 0-20 wt.%, based on the weight of the ink;
(c) a pigment, present in the amount of 2-30 wtA, preferably 5-20 wtA, based on the weight of the ink; and (d) a re-wetting agent, present in the amount of 0.5-10 wtA, based on the weight of the ink.
Examples of suitable macromolecular binders which are soluble in the water phase of the ink regardless of the pH of the water phase include: carboxymethyl-cellulose, hydroxyethylcellulose, hydroxypropyl-cellulose, hydroxybutylmethylcellulose, poly(C1-C4) alkylene oxides, polyethyleneimine, polyvinyl alcohol, polyvinyl acetate, polyvinylpyrollidone, polyvinyl-oxazolidone and polyacrylamide polymers.
Preferably, the macromolecular binders present in the ink are only those macromolecular binders which are soluble in the water phase only at a pre-determined pH
value. Such pH value may be acidic, e.g. about 2.5 to about 6.5, but is preferably in the range of about 7.5 to about 10. Suitable examples of such macromolecular binders include methacrylic resins; styrene-acrylic resins; rosin salts; and polystyrenesulfonic acid and its salts. Ammonia or an organic amine such as monoethanol-amine or N,N-diethanolamine may be added to the water phase in order to adjust the pH to the preferred value (a mineral acid or an organic acid such as acetic acid may be used to adjust the pH to a value in the range of about 2.5 to about 6.5).
Suitable examples of the macromolecular binders comprising aqueous emulsions include acrylic or vinyl emulsion polymers prepared from monomers selected from the group consisting of acrylic acid esters, methacrylic acid esters, acrylic acid esters of polyhydric alcohols, methyl methacrylate, styrene, vinyl styrene and vinyl acetate.
The pigment may be any of those which are suitable for formulating offset lithographic printing inks such as CI Pigment Yellows 1, 3, 4, 5, 12, 13, 14, 17, 55, 65, 73, 83, 97 and 98; CI Pigment oranges 13, 16 and 46; CI
CA 02242561 1998 07-09r% 97 ~ v~=~
Pigment Reds 2, 3, 4, 10, 12, 48, 48:1, 48:2, 53, 57:2, 81, 104, 146, 170 and 176; CI Pigment Greens 2, 7 and 36;CI Pigment Blues 1, 15:1, 15:2, 15:3, 15:6, 16, 29, 56 and 61; CI Pigment Violets 3, 23 and 37; CI Pigment Blacks 6 and 7; and CI Pigment Whites 6, 7, 18 and 26.
Suitable examples of rewetting agents include urea, thiourea, hydroxyethylethylene urea, glycerol, sorbitol, ethylene glycol and butyl carbitol.
Preferably, the water-based printing ink will include a nonionic surfactant, present in the amount of 1s up to 5 wtA, based on the weight of the ink. Suitable examples of the surfactant include acetylenic glycols, ethoxylated glycols and sorbitan esters.
If desired, the usual adjuvants such as waxes, antifoam agents, biocides, corrosion inhibitors, etc.
may be incorporated in the water-based printing ink.
Offset lithographic printing presses having the controls for-achieving such desirable relative humidity and temperature levels during the printing process are not within the purview of this invention.
A printing press which could efficiently carry out the offset lithographic printing process of the invention might have the following features:
a) an inking mechanism for applying the ink to the print cylinder;
b) a housing surrounding the inking mechanism and the print cylinder so as to define an enclosed space;
133M Q3Ot3M
c) a cooling mechanism for cooling the atmosphere within the enclosed space;
d) a humidifier for controlling the humidity of the atmosphere within the enclosed space; and e) means for introducing a chemical substance such as ammonium hydroxide or anhydrous ammonia or an amine such as ethanolamine into the enclosed space in order to insure that the pH is maintained at a desired value of about 7.5 to about 10 (if an acidic pH value is desired, the chemical substance may be a mineral acid or an organic acid such as acetic acid); maintenance of the pH within such range will minimize the likelihood that the water-based ink described above will dry out on the rollers during operation of the press (the water-based inks described above contain macromolecular binders which are predominantly or wholly of the type which are soluble in the water phase of the ink only at a pre-determined desired pH value).
A printing press having the features such as those set forth above would likely also contain sensors and valving mechanisms to insure that the desired temperature, humidity and pH value of the ink are continuously monitored and adjusted as may be necessary throughout the course of the printing operation.
The offset lithographic printing process of the present invention are further illustrated by the following non-limiting examples in which all parts and percentages are by weight, unless otherwise indicated.
Example 1 A water-based ink was prepared from the components indicated below. The water phase of the ink was supplied by the water present in the acrylic resin latex, hydroxy-propyl cellulose, hydroxyethylethylene urea and the maleated rosin ester:
Com,ponent Amount, wtA
Styrene/maleic anhydride resin 12 Phthalocyanine Blue pigment 12 Acrylic resin latex (50 wtA solids) 5 Hydroxypropylcellulose (3 wtA solids) 10 Hydroxyethylethylene urea (70 wtA solids) 8 Monoethanol amine 2 Polyethylene Wax 2 Ethoxylated acetylenic diol surfactant 2 Maleated rosin ester (50 wt.% solids) 47 Total 100 The printing ink was printed using a Didde press whose printing units, printing plate and printing blankets were enclosed within a chamber in order to control the relative humidity and temperature during the press run.
The printing plate was obtained from Toray industries; the image area of the aluminum oxide substrate was coated with a photopolymer whose surface was hydrophilic in nature, while the non-image area was coated with a silicone polymer. The press run was carried out at a relative humidity in the range of 85-90%
and a temperature in the range of 15-20 C and the press speed was 1,000 feet/minute (about 500 cm/second).
The prints obtained from this press run were clear and sharp. The print density was 1.5 and the dot gain was 15%. There was no discernible toning in the non-image area.
Preferably, the macromolecular binders present in the ink are only those macromolecular binders which are soluble in the water phase only at a pre-determined pH
value. Such pH value may be acidic, e.g. about 2.5 to about 6.5, but is preferably in the range of about 7.5 to about 10. Suitable examples of such macromolecular binders include methacrylic resins; styrene-acrylic resins; rosin salts; and polystyrenesulfonic acid and its salts. Ammonia or an organic amine such as monoethanol-amine or N,N-diethanolamine may be added to the water phase in order to adjust the pH to the preferred value (a mineral acid or an organic acid such as acetic acid may be used to adjust the pH to a value in the range of about 2.5 to about 6.5).
Suitable examples of the macromolecular binders comprising aqueous emulsions include acrylic or vinyl emulsion polymers prepared from monomers selected from the group consisting of acrylic acid esters, methacrylic acid esters, acrylic acid esters of polyhydric alcohols, methyl methacrylate, styrene, vinyl styrene and vinyl acetate.
The pigment may be any of those which are suitable for formulating offset lithographic printing inks such as CI Pigment Yellows 1, 3, 4, 5, 12, 13, 14, 17, 55, 65, 73, 83, 97 and 98; CI Pigment oranges 13, 16 and 46; CI
CA 02242561 1998 07-09r% 97 ~ v~=~
Pigment Reds 2, 3, 4, 10, 12, 48, 48:1, 48:2, 53, 57:2, 81, 104, 146, 170 and 176; CI Pigment Greens 2, 7 and 36;CI Pigment Blues 1, 15:1, 15:2, 15:3, 15:6, 16, 29, 56 and 61; CI Pigment Violets 3, 23 and 37; CI Pigment Blacks 6 and 7; and CI Pigment Whites 6, 7, 18 and 26.
Suitable examples of rewetting agents include urea, thiourea, hydroxyethylethylene urea, glycerol, sorbitol, ethylene glycol and butyl carbitol.
Preferably, the water-based printing ink will include a nonionic surfactant, present in the amount of 1s up to 5 wtA, based on the weight of the ink. Suitable examples of the surfactant include acetylenic glycols, ethoxylated glycols and sorbitan esters.
If desired, the usual adjuvants such as waxes, antifoam agents, biocides, corrosion inhibitors, etc.
may be incorporated in the water-based printing ink.
Offset lithographic printing presses having the controls for-achieving such desirable relative humidity and temperature levels during the printing process are not within the purview of this invention.
A printing press which could efficiently carry out the offset lithographic printing process of the invention might have the following features:
a) an inking mechanism for applying the ink to the print cylinder;
b) a housing surrounding the inking mechanism and the print cylinder so as to define an enclosed space;
133M Q3Ot3M
c) a cooling mechanism for cooling the atmosphere within the enclosed space;
d) a humidifier for controlling the humidity of the atmosphere within the enclosed space; and e) means for introducing a chemical substance such as ammonium hydroxide or anhydrous ammonia or an amine such as ethanolamine into the enclosed space in order to insure that the pH is maintained at a desired value of about 7.5 to about 10 (if an acidic pH value is desired, the chemical substance may be a mineral acid or an organic acid such as acetic acid); maintenance of the pH within such range will minimize the likelihood that the water-based ink described above will dry out on the rollers during operation of the press (the water-based inks described above contain macromolecular binders which are predominantly or wholly of the type which are soluble in the water phase of the ink only at a pre-determined desired pH value).
A printing press having the features such as those set forth above would likely also contain sensors and valving mechanisms to insure that the desired temperature, humidity and pH value of the ink are continuously monitored and adjusted as may be necessary throughout the course of the printing operation.
The offset lithographic printing process of the present invention are further illustrated by the following non-limiting examples in which all parts and percentages are by weight, unless otherwise indicated.
Example 1 A water-based ink was prepared from the components indicated below. The water phase of the ink was supplied by the water present in the acrylic resin latex, hydroxy-propyl cellulose, hydroxyethylethylene urea and the maleated rosin ester:
Com,ponent Amount, wtA
Styrene/maleic anhydride resin 12 Phthalocyanine Blue pigment 12 Acrylic resin latex (50 wtA solids) 5 Hydroxypropylcellulose (3 wtA solids) 10 Hydroxyethylethylene urea (70 wtA solids) 8 Monoethanol amine 2 Polyethylene Wax 2 Ethoxylated acetylenic diol surfactant 2 Maleated rosin ester (50 wt.% solids) 47 Total 100 The printing ink was printed using a Didde press whose printing units, printing plate and printing blankets were enclosed within a chamber in order to control the relative humidity and temperature during the press run.
The printing plate was obtained from Toray industries; the image area of the aluminum oxide substrate was coated with a photopolymer whose surface was hydrophilic in nature, while the non-image area was coated with a silicone polymer. The press run was carried out at a relative humidity in the range of 85-90%
and a temperature in the range of 15-20 C and the press speed was 1,000 feet/minute (about 500 cm/second).
The prints obtained from this press run were clear and sharp. The print density was 1.5 and the dot gain was 15%. There was no discernible toning in the non-image area.
Claims (13)
1. An offset lithographic printing process which is conducted at a relative humidity of 75-90%, said process utilizing a water-based, single fluid, fountain solution free, offset lithographic printing ink comprised of:
(a) 10 to 70 wt.% a macromolecular binder containing:
(i) macromolecular binders, soluble in the water phase regardless of the pH of the water, present in an amount of up to 5 wt.%;
(ii) macromolecular rosin salt binders, soluble in the water phase at a pH
ranging from 7.5 to 10, present in an amount of 10-70 wt.%; and (iii) macromolecular binders comprised of aqueous emulsions, present in an amount of up to 20 wt.%;
(b) a pigment, present in the amount of 2-30 wt.%; and (c) a re-wetting agent, present in the amount of 0.5-10 wt.%.
(a) 10 to 70 wt.% a macromolecular binder containing:
(i) macromolecular binders, soluble in the water phase regardless of the pH of the water, present in an amount of up to 5 wt.%;
(ii) macromolecular rosin salt binders, soluble in the water phase at a pH
ranging from 7.5 to 10, present in an amount of 10-70 wt.%; and (iii) macromolecular binders comprised of aqueous emulsions, present in an amount of up to 20 wt.%;
(b) a pigment, present in the amount of 2-30 wt.%; and (c) a re-wetting agent, present in the amount of 0.5-10 wt.%.
2. The process of claim 1, wherein the relative humidity is in the range of 80-85%.
3. The process of claim 1, wherein the process is conducted at a temperature in the range of 10 to 30°C.
4. The process of claim 3, wherein the process is conducted at a temperature in the range of 15 to 25°C.
5. The process of claim 1, wherein the macromolecular binder is present in an amount of 30-60 wt.%, based on the weight of the ink.
6. The process of claim 1, wherein the macromolecular binders which are soluble in the water phase regardless of the pH of the water phase are selected from the group consisting of:
carboxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxybutylmethylcellulose, poly(C1-C4)alkylene oxides, polyethyleneimine, polyvinyl alcohol, polyvinyl acetate, polyvinylpyrollidone, polyvinyloxazolidone, and polyacrylamide.
carboxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxybutylmethylcellulose, poly(C1-C4)alkylene oxides, polyethyleneimine, polyvinyl alcohol, polyvinyl acetate, polyvinylpyrollidone, polyvinyloxazolidone, and polyacrylamide.
7. The process of claim 1, wherein the macromolecular binders present in the ink consist of those macromolecular binders which are soluble in the water phase only at a pre-determined pH value.
8. The process of claim 1, wherein the macromolecular binders comprising aqueous emulsions are selected from the group consisting of acrylic or vinyl emulsion polymers prepared from monomers selected from the group consisting of acrylic acid esters, methacrylic acid esters, acrylic acid esters of polyhydric alcohols, methyl methacrylate, styrene, vinyl styrene, and vinyl acetate.
9. The process of claim 1, wherein the pigment is present in an amount of 5 to wt.%, based on the weight of the ink.
10. The process of claim 1, wherein the pigment is selected from the group consisting of CI Pigment Yellows 1, 3, 4, 5, 12, 13, 14, 17, 55, 65, 73, 83, 97, and 98;
CI Pigment Oranges 13, 16, and 46; CI Pigment Reds 2, 3, 4, 10, 12, 48, -48:1, 48:2, 53, 57:2, 81, 104, 146, 170, and 176; CI Pigment Greens 2, 7, and 36; CI Pigment Blues 1, 15:1, 15:2, 15:3, 15:6, 16, 29, 56, and 61; CI Pigment Violets 3, 23, and 37; CI Pigment Blacks 6 and 7; and CI
Pigment Whites 6, 7, 18, and 26.
CI Pigment Oranges 13, 16, and 46; CI Pigment Reds 2, 3, 4, 10, 12, 48, -48:1, 48:2, 53, 57:2, 81, 104, 146, 170, and 176; CI Pigment Greens 2, 7, and 36; CI Pigment Blues 1, 15:1, 15:2, 15:3, 15:6, 16, 29, 56, and 61; CI Pigment Violets 3, 23, and 37; CI Pigment Blacks 6 and 7; and CI
Pigment Whites 6, 7, 18, and 26.
11. The process of claim 1, wherein the rewetting agent is selected from the group consisting of urea, thiourea, hydroxyethylethylene urea, glycerol, sorbitol, ethylene glycol, and butyl carbitol.
12. The process of claim 1, wherein the ink further comprises a nonionic surfactant, present in an amount of up to 5 wt.%, based on the weight of the ink.
13. The process of claim 12, wherein the nonionic surfactant is selected from the group consisting of acetylenic glycols, ethoxylated glycols, and sorbitan esters.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/614,559 US5778789A (en) | 1996-03-13 | 1996-03-13 | Offset lithographic printing process with a water based ink |
| US08/614,559 | 1996-03-13 | ||
| PCT/US1997/003868 WO1997033757A1 (en) | 1996-03-13 | 1997-03-13 | Offset lithographic printing process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2242561A1 CA2242561A1 (en) | 1997-09-18 |
| CA2242561C true CA2242561C (en) | 2007-08-21 |
Family
ID=38434616
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002242561A Expired - Fee Related CA2242561C (en) | 1996-03-13 | 1997-03-13 | Offset lithographic printing process |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2242561C (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105818517B (en) * | 2015-01-05 | 2018-03-30 | 中国科学院化学研究所 | A kind of water-based ink lithographic system |
-
1997
- 1997-03-13 CA CA002242561A patent/CA2242561C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2242561A1 (en) | 1997-09-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5778789A (en) | Offset lithographic printing process with a water based ink | |
| EP0886670B1 (en) | Water-based offset lithographic printing ink | |
| US6200372B1 (en) | Water-based offset lithographic newspaper printing ink | |
| EP2035515B1 (en) | Water washable lithographic printing ink | |
| US5972088A (en) | Water-based gravure printing ink | |
| US6131514A (en) | Method of making a printing plate with an ink jet fluid material | |
| US5417749A (en) | Microemulsion printing ink | |
| US6444021B1 (en) | Water washable lithographic newspaper printing ink | |
| US6444022B1 (en) | Water based offset lithographic printing ink | |
| JP2004066816A (en) | Manufacturing method for printing plate | |
| CA2242561C (en) | Offset lithographic printing process | |
| EP1461394B1 (en) | Water-based offset lithographic printing inks containing polymerizable surfactants | |
| EP1285033A2 (en) | Latex polymer based printing ink | |
| CA2297045A1 (en) | Water-based offset lithographic newspaper printing ink | |
| JP2002265838A (en) | Water-based offset lithography ink for printing newspaper | |
| US7674327B2 (en) | Flexographic ink compositions |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed | ||
| MKLA | Lapsed |
Effective date: 20110314 |