EP0756942A1 - Procédé de formation d'images par ablation à laser - Google Patents
Procédé de formation d'images par ablation à laser Download PDFInfo
- Publication number
- EP0756942A1 EP0756942A1 EP96420241A EP96420241A EP0756942A1 EP 0756942 A1 EP0756942 A1 EP 0756942A1 EP 96420241 A EP96420241 A EP 96420241A EP 96420241 A EP96420241 A EP 96420241A EP 0756942 A1 EP0756942 A1 EP 0756942A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dye
- infrared
- soluble
- water
- layer
- 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.)
- Withdrawn
Links
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
- B41C1/1008—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials
- B41C1/1033—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials by laser or spark ablation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/24—Ablative recording, e.g. by burning marks; Spark recording
Definitions
- This invention relates to process for obtaining a single color element for laser-induced, dye-ablative imaging and, more particularly, to a method for generating optical masks and monochrome transparencies used in graphic arts.
- thermal transfer systems have been developed to obtain prints from pictures which have been generated electronically from a color video camera.
- an electronic picture is first subjected to color separation by color filters.
- the respective color-separated images are then converted into electrical signals.
- These signals are then operated on to produce cyan, magenta and yellow electrical signals.
- These signals are then transmitted to a thermal printer.
- a cyan, magenta or yellow dye-donor element is placed face-to-face with a dye-receiving element.
- the two are then inserted between a thermal printing head and a platen roller.
- a line-type thermal printing head is used to apply heat from the back of the dye-donor sheet.
- the thermal printing head has many heating elements and is heated up sequentially in response to the cyan, magenta and yellow signals. The process is then repeated for the other two colors. A color hard copy is thus obtained which corresponds to the original picture viewed on a screen. Further details of this process and an apparatus for carrying it out are contained in U.S. Patent No. 4,621,271.
- the donor sheet includes a material which strongly absorbs at the wavelength of the laser.
- this absorbing material converts light energy to thermal energy and transfers the heat to the dye in the immediate vicinity, thereby heating the dye to its vaporization temperature for transfer to the receiver.
- the absorbing material may be present in a layer beneath the dye and/or it may be admixed with the dye.
- the laser beam is modulated by electronic signals which are representative of the shape and color of the original image, so that each dye is heated to cause volatilization only in those areas in which its presence is required on the receiver to reconstruct the color of the original object. Further details of this process are found in GB 2,083,726A.
- an element with a dye layer composition comprising an image dye, an infrared-absorbing material, and a binder coated onto a substrate is imaged from the dye side.
- the energy provided by the laser drives off the image dye at the spot where the laser beam hits the element and leaves the binder behind.
- the laser radiation causes rapid local changes in the imaging layer thereby causing the material to be ejected from the layer. This is distinguishable from other material transfer techniques in that some sort of chemical change (e.g., bond-breaking), rather than a completely physical change (e.g., melting, evaporation or sublimation), causes an almost complete transfer of the image dye rather than a partial transfer.
- the transmission Dmin density serves as a measure of the completeness of image dye removal by the laser. Examples of this type of ablative imaging is found in U.S. Patent 5,429,909.
- the dye-ablative recording element is exposed by a laser which causes the hydrophilic, water-soluble, infrared-absorbing layer and the hydrophobic dye-barrier layer to be ablated, melted, pushed aside, or otherwise removed by laser heating, thereby uncovering the underlying hydrophilic dye-receiving layer.
- the dye-receiving layer soaks up imaging dye from the solution preferentially in the exposed regions, thus providing a contrast difference between exposed and unexposed areas.
- the water-soluble, infrared-absorbing layer is washed away and with it all remaining infrared-absorbing material, which then will no longer contribute to the Dmin of the resulting image.
- the advantage of this invention is that high contrast images with low Dmin can be achieved with much lower exposure than achievable with conventional dye ablation imaging.
- Another advantage of this invention is that high-contrast, monocolor images can be achieved with a low exposure to produce a negative-working image system.
- a negative-working system has an advantage when used in conjunction with another negative-working imaging material (such as when used as a mask for making printing plates or contact duplicates). In this case the background need not be exposed, thus saving time and energy for many images.
- the hydrophobic dye-barrier layer employed in the invention can be made relatively thin since it does not contain image dyes and, therefore, requires little energy to be removed. This is in contrast to a thick dye layer used in conventional ablation films which requires more energy to be removed.
- the dye-barrier layer can be from about 0.01 ⁇ m to about 5 ⁇ m in thickness, preferably from about 0.05 ⁇ m to about 1 ⁇ m.
- the contrast between exposed and unexposed areas in the element can be controlled by variables, such as laser exposure, time of contact with the ink solution, concentration of the ink solution, thickness of the dye-receiving layer, and diffusion properties of the dye within the dye-receiving layer.
- the process of the invention is especially useful in making reprographic masks which are used in publishing and in the generation of printed circuit boards.
- the masks are placed over a photosensitive material, such as a printing plate, and exposed to a light source.
- the photosensitive material usually is activated only by certain wavelengths.
- the photosensitive material can be a polymer which is crosslinked or hardened upon exposure to ultraviolet or blue light but is not affected by red or green light.
- the mask which is used to block light during exposure, must absorb all wavelengths which activate the photosensitive material in the Dmax regions and absorb little in the Dmin regions.
- a diode laser is preferably employed since it offers substantial advantages in terms of its small size, low cost, stability, reliability, ruggedness, and ease of modulation.
- the element before any laser can be used to heat an ablative recording element, the element must contain an infrared-absorbing material, such as pigments like carbon black, or cyanine infrared-absorbing dyes as described in U.S. Patent 4,973,572, or other materials as described in the following U.S. Patent Numbers: 4,948,777, 4,950,640, 4,950,639, 4,948,776, 4,948,778, 4,942,141, 4,952,552, 5,036,040, and 4,912,083.
- the laser radiation is then absorbed into the hydrophilic, water-soluble light-absorbing layer and converted to heat by a molecular process known as internal conversion.
- the dyes in the aqueous ink solution which can be used in the process of the invention can be any water-soluble dye known in the art, such as, for example, nigrosin black, crystal violet, azure c, azure a, acid red 103, basic orange 21, acriflavine, acid red 88, acid red 4, direct yellow 62, direct yellow 29, basic blue 16, lacmoid, litmus, saffron, rhodamine 6g.
- the above dyes are available from Aldrich Chemical Co.
- the aqueous ink solution may be applied to the recording element by either bathing the element in a solution of the dye or applying the dye by a sponge, squeegee, roller or other applicator.
- the hydrophobic dye-barrier layer material used in the invention can be, for example, nitrocellulose, cellulose acetate propionate, cellulose acetate, polymethylmethacrylate, polyacrylates, polystyrenes, polysulfones, polycyanoacrylates, etc.
- ablation enhancers such as blowing agents, e.g., azides, accelerators, e.g., 4,4'-diazidobenzophenone and 2,6-di(4-azidobenzal)-4-methylcyclohexanone, or the materials disclosed in U.S. Patent 5,256,506.
- the hydrophilic dye-receiving layer used in the process of the invention is a water-insoluble polymer such as a high molecular weight and/or crosslinked polymer, e.g., a high molecular weight and/or crosslinked gelatin, xanthum gum (available commercially as Keltrol T® from Kelco-Merck Co.), poly(vinyl alcohol), polyester ionomers, polyglycols, polyacrylamides, polyalkylidene-etherglycols, polyacrylates with amine, hydroxyl or carboxyl side groups, etc.
- a water-insoluble polymer such as a high molecular weight and/or crosslinked polymer, e.g., a high molecular weight and/or crosslinked gelatin, xanthum gum (available commercially as Keltrol T® from Kelco-Merck Co.), poly(vinyl alcohol), polyester ionomers, polyglycols, polyacrylamides, polyalkylidene-etherglycol
- the hydrophilic, water-soluble, infrared-absorbing layer can contain an infrared-absorbing material and a polymeric binder such as, for example, a polymer having a sufficiently low molecular weight to render it water-soluble such as a low molecular weight gelatin, a poly(vinyl alcohol), a polyester ionomer, a polyglycol, a polyacrylamide, a polyalkylidene-etherglycol, a polyacrylate with amine, hydroxyl or carboxyl side groups, etc.
- a polymeric binder such as, for example, a polymer having a sufficiently low molecular weight to render it water-soluble such as a low molecular weight gelatin, a poly(vinyl alcohol), a polyester ionomer, a polyglycol, a polyacrylamide, a polyalkylidene-etherglycol, a polyacrylate with amine, hydroxyl or carboxyl side groups, etc.
- the infrared-absorbing material in the hydrophilic, water-soluble, infrared-absorbing layer can be a water-soluble infrared-absorbing dye such as IR-1 (shown hereinafter), Naphthol Green B (acid Green 1), Indocyanine green, sulfonated or carboxylated metal phthalacyanines, etc.
- the infrared-absorbing material can also be a pigment such as carbon black dispersed in the water-soluble binder.
- the hydrophilic, water-soluble, infrared-absorbing layer can just be the water-soluble infrared-absorbing dye alone without any binder.
- any material can be used as the support for the ablative recording element employed in the invention provided it is dimensionally stable and can withstand the heat of the laser.
- Such materials include polyesters such as poly(ethylene naphthalate); poly(ethylene terephthalate); polyamides; polycarbonates; cellulose esters; fluorine polymers; polyethers; polyacetals; polyolefins; and polyimides.
- the support generally has a thickness of from about 5 to about 200 ⁇ m. In a preferred embodiment, the support is transparent.
- a control coating of 0.054 g/m 2 of IR-2 with and without binder (Keltrol T®, a xanthum gum from Kelco-Merck & Co., Inc.) was coated on 100 ⁇ m poly(ethylene terephthalate) from Eastman Chemical Co.
- the Status A Red and Green densities were measured, as shown in the Table below.
- An aqueous coating was prepared by dissolving aqueous-compatible polymers (shown in the Table) in water, knife-coating the solution on 100 ⁇ m poly(ethylene terephthalate) support and drying to produce a dried coating containing 1.08 g/m 2 of polymer.
- N-(NC) (0.108 g/m 2 ) and 0.054 g/m 2 IR-2 absorber dye were coated from acetone over the dye-receiving layer as indicated in the Table.
- Ten samples according to the invention were prepared as follows:
- An aqueous coating was prepared by dissolving aqueous-compatible polymers (see Table) in water, knife-coating the solution on 100 ⁇ m poly(ethylene terephthalate) support and drying to produce a dried coating containing 1.08 g/m 2 of polymer.
- a solvent coating was prepared by dissolving solvent-compatible polymers in acetone and knife-coating the solution over the dye-receiving layer to produce a dried layer containing a weight of solid material as indicated in the Table.
- a thin aqueous coating was prepared by dissolving IR-1 in water and knife-coating the solution over the dye-barrier layer (Samples 1-3 and 7).
- Samples 4-6 and 8-10 aqueous-compatible polymers were added to the solution (see Table).
- the samples were exposed using Spectra Diode Labs Lasers Model SDL-2432, having an integral, attached fiber for the output of the laser beam with a wavelength range of 800-830 nm and a nominal power output of 250 mW at the end of the optical fiber.
- the cleaved face of the optical fiber was imaged onto the plane of the element with a 0.5 magnification lens assembly mounted on a translation stage giving a nominal spot size of 25 ⁇ m.
- the translation stage was incrementally advanced across the film element by means of a lead screw turned by a microstepping motor, to give a center-to-center line distance of 10 ⁇ m (945 lines per cm, or 2400 lines per in.).
- An air stream was blown over the donor surface to remove the ablated material.
- the measured total power at the focal point was 100 mW.
- the hue associated with the IR dyes was removed from the background as illustrated by the comparison of the samples with Controls 1 and 2.
- Control 2 shows that unwanted hue due to the IR dye remains after processing in the background when the IR dye is not in a separate water-soluble top layer, as indicated by the higher red vs. green density in Dmin.
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- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Electronic Switches (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US620696 | 1990-12-03 | ||
US1443 | 1993-01-07 | ||
US144395P | 1995-07-26 | 1995-07-26 | |
US08/620,696 US5633118A (en) | 1996-03-21 | 1996-03-21 | Laser ablative imaging method |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0756942A1 true EP0756942A1 (fr) | 1997-02-05 |
Family
ID=26669033
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP96420241A Withdrawn EP0756942A1 (fr) | 1995-07-26 | 1996-07-18 | Procédé de formation d'images par ablation à laser |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0756942A1 (fr) |
JP (1) | JPH09104174A (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5856061A (en) * | 1997-08-14 | 1999-01-05 | Minnesota Mining And Manufacturing Company | Production of color proofs and printing plates |
WO2003106164A1 (fr) * | 2002-06-17 | 2003-12-24 | Institut für Neue Materialien Gemeinnützige GmbH | Substrat presentant une surface structuree comprenant des zones hydrophobes et des zones hydrophiles |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6327091B1 (en) | 1999-01-18 | 2001-12-04 | Fuji Photo Film Co., Ltd. | Collimating plate and backlight system |
US6778239B2 (en) | 1999-01-18 | 2004-08-17 | Fuji Photo Film Co., Ltd. | Light diffusing plate and display apparatus |
Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2415324A1 (fr) * | 1978-01-23 | 1979-08-17 | Du Pont | Elements photopolymerisables ayant des images hydrophiles et oleophiles a colorant absorbe selectivement |
EP0101266A2 (fr) * | 1982-08-09 | 1984-02-22 | Milliken Research Corporation | Procédé et appareil pour l'impression |
US4621271A (en) | 1985-09-23 | 1986-11-04 | Eastman Kodak Company | Apparatus and method for controlling a thermal printer apparatus |
US4912083A (en) | 1989-06-20 | 1990-03-27 | Eastman Kodak Company | Infrared absorbing ferrous complexes for dye-donor element used in laser-induced thermal dye transfer |
US4942141A (en) | 1989-06-16 | 1990-07-17 | Eastman Kodak Company | Infrared absorbing squarylium dyes for dye-donor element used in laser-induced thermal dye transfer |
US4948777A (en) | 1989-06-16 | 1990-08-14 | Eastman Kodak Company | Infrared absorbing bis(chalcogenopyrylo)polymethine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4948778A (en) | 1989-06-20 | 1990-08-14 | Eastman Kodak Company | Infrared absorbing oxyindolizine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4948776A (en) | 1989-06-16 | 1990-08-14 | Eastman Kodak Company | Infrared absorbing chalcogenopyrylo-arylidene dyes for dye-donor element used in laser-induced thermal dye transfer |
US4950640A (en) | 1989-06-16 | 1990-08-21 | Eastman Kodak Company | Infrared absorbing merocyanine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4950639A (en) | 1989-06-16 | 1990-08-21 | Eastman Kodak Company | Infrared absorbing bis(aminoaryl)polymethine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4952552A (en) | 1989-06-20 | 1990-08-28 | Eastman Kodak Company | Infrared absorbing quinoid dyes for dye-donor element used in laser-induced thermal dye transfer |
US4973572A (en) | 1987-12-21 | 1990-11-27 | Eastman Kodak Company | Infrared absorbing cyanine dyes for dye-donor element used in laser-induced thermal dye transfer |
US5036040A (en) | 1989-06-20 | 1991-07-30 | Eastman Kodak Company | Infrared absorbing nickel-dithiolene dye complexes for dye-donor element used in laser-induced thermal dye transfer |
US5256506A (en) | 1990-10-04 | 1993-10-26 | Graphics Technology International Inc. | Ablation-transfer imaging/recording |
EP0580393A2 (fr) * | 1992-07-20 | 1994-01-26 | Presstek, Inc. | Plaque pour l'impression lithographique |
US5429909A (en) | 1994-08-01 | 1995-07-04 | Eastman Kodak Company | Overcoat layer for laser ablative imaging |
-
1996
- 1996-07-18 EP EP96420241A patent/EP0756942A1/fr not_active Withdrawn
- 1996-07-26 JP JP19759696A patent/JPH09104174A/ja active Pending
Patent Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2415324A1 (fr) * | 1978-01-23 | 1979-08-17 | Du Pont | Elements photopolymerisables ayant des images hydrophiles et oleophiles a colorant absorbe selectivement |
EP0101266A2 (fr) * | 1982-08-09 | 1984-02-22 | Milliken Research Corporation | Procédé et appareil pour l'impression |
US4621271A (en) | 1985-09-23 | 1986-11-04 | Eastman Kodak Company | Apparatus and method for controlling a thermal printer apparatus |
US4973572A (en) | 1987-12-21 | 1990-11-27 | Eastman Kodak Company | Infrared absorbing cyanine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4950640A (en) | 1989-06-16 | 1990-08-21 | Eastman Kodak Company | Infrared absorbing merocyanine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4948777A (en) | 1989-06-16 | 1990-08-14 | Eastman Kodak Company | Infrared absorbing bis(chalcogenopyrylo)polymethine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4948776A (en) | 1989-06-16 | 1990-08-14 | Eastman Kodak Company | Infrared absorbing chalcogenopyrylo-arylidene dyes for dye-donor element used in laser-induced thermal dye transfer |
US4942141A (en) | 1989-06-16 | 1990-07-17 | Eastman Kodak Company | Infrared absorbing squarylium dyes for dye-donor element used in laser-induced thermal dye transfer |
US4950639A (en) | 1989-06-16 | 1990-08-21 | Eastman Kodak Company | Infrared absorbing bis(aminoaryl)polymethine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4948778A (en) | 1989-06-20 | 1990-08-14 | Eastman Kodak Company | Infrared absorbing oxyindolizine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4952552A (en) | 1989-06-20 | 1990-08-28 | Eastman Kodak Company | Infrared absorbing quinoid dyes for dye-donor element used in laser-induced thermal dye transfer |
US4912083A (en) | 1989-06-20 | 1990-03-27 | Eastman Kodak Company | Infrared absorbing ferrous complexes for dye-donor element used in laser-induced thermal dye transfer |
US5036040A (en) | 1989-06-20 | 1991-07-30 | Eastman Kodak Company | Infrared absorbing nickel-dithiolene dye complexes for dye-donor element used in laser-induced thermal dye transfer |
US5256506A (en) | 1990-10-04 | 1993-10-26 | Graphics Technology International Inc. | Ablation-transfer imaging/recording |
EP0580393A2 (fr) * | 1992-07-20 | 1994-01-26 | Presstek, Inc. | Plaque pour l'impression lithographique |
US5429909A (en) | 1994-08-01 | 1995-07-04 | Eastman Kodak Company | Overcoat layer for laser ablative imaging |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5856061A (en) * | 1997-08-14 | 1999-01-05 | Minnesota Mining And Manufacturing Company | Production of color proofs and printing plates |
WO2003106164A1 (fr) * | 2002-06-17 | 2003-12-24 | Institut für Neue Materialien Gemeinnützige GmbH | Substrat presentant une surface structuree comprenant des zones hydrophobes et des zones hydrophiles |
Also Published As
Publication number | Publication date |
---|---|
JPH09104174A (ja) | 1997-04-22 |
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