This disclosure relates to printing; particularly to flexographic printing; and more particularly to high resolution flexographic printing.
Delivery of inks to flexographic printing plates is an important part of a flexographic printing technology. Typically, ink delivery uses anilox rolls that have an exposed surface built out of small cells. These cells are filled with ink by dipping the roll into a pan filled with ink and then doctoring off excess ink with a blade. Ink from cells of the anilox roll is transferred to raised features of a flexographic printing plate. The smallest cell size of an anilox roll currently available is about 20 micrometers for 1200 line screen anilox rolls or about 15 micrometers for 1600 dpi rolls. Significant challenges are present when inking flexographic features having lateral dimensions smaller than 20 micrometers. For example, as the difference in size between the anilox roll cell and the feature increases, the variability in the amount of ink that the feature picks up also would likely increase. At least in part, this variability can be attributed to the relative position of the feature and the cell. As such, the ability to achieve finer resolution printing with flexographic systems has been hindered.
The disclosure presented herein describes methods and systems for improved transfer of material from a donor substrate to a feature of a flexographic printing plate.
In an embodiment, a method for flexographic printing is described. The method comprises removing at least a portion of a solvent from a material to achieve a reduced-solvent material. The material may be disposed onto a donor substrate, e.g. by die coating, and the solvent removed while the material is on the donor substrate. The method further comprises disposing the reduced-solvent material onto a feature of a flexographic printing plate. The reduced-solvent material may be disposed onto the feature by transferring reduced-solvent material from the donor substrate to the feature. Any amount of solvent removal is expected to result in more uniform amounts of reduced-solvent material being disposed on the feature of the flexographic printing plate. In some cases removing at least 10% of the solvent may be appropriate. In other cases, removing at least 50%, 90%, 95%, 99%, or substantially all of the solvent may be desired. The method further comprises transferring the reduced-solvent material from the feature of the flexographic printing plate to a recipient substrate. The reduced-solvent substrate may then be cured on the recipient substrate. The method is useful for features of any size. However, the advantages of the method may be more recognized when using features having a lateral dimension of 15 micrometers or less; e.g., 10 micrometers or less, or 5 micrometers or less.
In an embodiment, a method for flexographic printing is described. The method comprises disposing onto a donor substrate a material comprising a solvent; removing at least a portion of the solvent from the material on the donor substrate to achieve a reduced-solvent material; transferring the reduced-solvent material from the donor substrate to a feature of a flexographic printing plate; and transferring the reduced-solvent material from the feature to a recipient substrate. The method further comprises
In an embodiment, a flexographic printing system is described. The system comprises a donor substrate configured to receive a material such that the material is disposed onto the donor substrate. The donor substrate may be in the form of a surface of an inking roll, which surface is smooth or substantially smooth. The material comprises a solvent. The system further comprises a solvent removal apparatus capable of removing the solvent from the material disposed onto the donor substrate to produce a reduced-solvent material disposed onto the donor substrate. The system also comprises a flexographic roll configured to attachably receive a flexographic printing plate comprising a feature. The flexographic roll is moveable relative to the donor substrate to allow the reduced-solvent material on the donor substrate to be transferred to the feature of the printing plate. The system further comprises a backup roll positioned relative to the flexographic roll such that movement of the backup roll relative to the flexographic roll is capable of causing a recipient substrate to move between the backup roll and the flexographic roll to allow the reduced-solvent substrate to be transferred from the feature to the recipient substrate. The system may further comprise an imprint reducing apparatus for reducing imprints on the donor substrate that result from transfer of the reduced-solvent material from the donor substrate to the feature of the plate. The system is useful for flexographic printing plates having features of any size. However, the advantages of the system may be more recognized when using plates having features with a lateral dimension of 15 micrometers or less; e.g., 10 micrometers or less or 5 micrometers or less.
Removing solvent from a material on a donor substrate prior to transfer to a feature of a flexographic printing plate provides several advantages. For example, removing solvent from a material to be transferred from a donor substrate to a recipient substrate by a feature of a flexographic printing plate should result in improved consistency of transfer of material from the donor substrate to the feature, particularly where the feature has a small lateral dimension. In addition, the use of a solvent-based material facilitates deposition of the material on the donor substrate, which can add to the uniformity of the amount of material transferred from the donor substrate to the feature. By reducing solvent in the material, the properties of the material, e.g. viscosity, thickness, adhesion, tack, etc., may be changed from properties desirable for disposing on a donor substrate to properties more desirable for disposing on a feature of a flexographic printing plate. These and other advantages of the systems and methods described herein are now evident or will become evident upon reading the description that follows.
The figures are not necessarily to scale. Like numbers used in the figures refer to like components, steps and the like. However, it will be understood that the use of a number to refer to a component in a given figure is not intended to limit the component in another figure labeled with the same number.
In the following description, reference is made to the accompanying drawings that form a part hereof, and in which are shown by way of illustration several specific embodiments. It is to be understood that other embodiments are contemplated and may be made without departing from the scope or spirit of the present invention. The following detailed description, therefore, is not to be taken in a limiting sense.
For the methods and systems described herein, removal of a solvent from a material to form a reduced-solvent material prior to transfer to a feature of a flexographic printing plate results in improved transfer of material to the feature, relative to transfer of similar material in which solvent has not been removed. While this is the case for flexographic printing plates having features of any size, the benefits of transfer of reduced-solvent material will be more evident with features having smaller lateral dimensions. In part this is because existing flexographic printing systems are quite good at transferring uniform amounts of material from a donor substrate, such as an anilox roll, to a feature of a flexographic printing plate, where the flexographic printing plate has a lateral dimension greater than about 20 micrometers. However, as the lateral dimensions of the feature decreases much beyond the current limitations of the size of the cells of an anilox roll; i.e., less than about 15 micrometers, the uniformity of transfer of a material comprising a high concentration of solvent decreases. A countervailing concern is that it becomes more difficult to dispose material on a donor substrate as the concentration of solvent is reduced. The present disclosure describes methods and systems that account for these opposing difficulties by removal of solvent from a material prior to transferring a material from a donor substrate to a feature of a flexographic printing plate.
The methods and systems described herein may be used with flexographic printing plates having features of any size. However, the advantages of the methods and systems may be more recognized when using features having lateral dimensions of 15 micrometers or less; e.g., 10 micrometers or less, or 5 micrometers or less. Flexographic plates having features with lateral dimensions of 15 micrometers or less may be as described in, e.g., U.S. Provisional Patent Application Ser. No. 60/865,979, Attorney Docket No. 62622US002, entitled “SOLVENT-ASSISTED EMBOSSING OF FLEXOGRAPHIC PRINTING PLATES” to Mikhail Pekurovsky et al., filed on even date herewith, which application is incorporated herein by reference in its entirety to the extent it does not contradict the disclosure presented herein.
All scientific and technical terms used herein have meanings commonly used in the art unless otherwise specified. The definitions provided herein are to facilitate understanding of certain terms used frequently herein and are not meant to limit the scope of the present disclosure.
As used herein, “flexographic printing” means a rotary printing process using a flexible printing plate; i.e., a flexographic printing plate. Any material that may be transferred from a flexographic printing plate to a recipient substrate may be “printed”.
As used herein, a “material” to be printed means a composition that is capable of being transferred from a feature of a flexographic printing plate to a recipient substrate. A material may comprise a solvent, and the components of the material may be dissolved, dispersed, suspended, or the like in the solvent.
As used herein, “reduced-solvent material” means a material from which at least a portion of a solvent has been removed. The solvent may be removed actively or passively.
As used herein, “flexographic printing plate” refers to a printing plate having features onto which material to be transferred to a recipient substrate may be disposed, wherein the plate or the features are capable of deforming when contacting the recipient substrate (relative to when not contacting the recipient substrate). A flexographic printing plate may be a flat plate that can be attached to a roll; e.g., by mounting tape, or a sleeve attached to a chuck, such as with Dupont™ CYREL® round plates.
As used herein, “feature” means a raised projection of a flexographic printing plate. The raised projection has a distal surface (or land), removed from the bulk of the flexographic printing plate, on which material may be disposed.
As used herein, “donor substrate” means a substrate onto which a material transferable to a feature of a flexographic printing plate may be disposed. Donor substrates may be in any form suitable for the transfer of material to a feature. For example, donor substrates may be films, plates or rolls.
As used herein, “recipient substrate” means a substrate onto which a material may be printed. Exemplary substrates include but are not limited to inorganic substrates such as quartz, glass, silica and other oxides or ceramics such as alumina, indium tin oxide, lithium tantalate (LiTaO.sub.3), lithium niobate (LiNbO.sub.3), gallium arsenide (GaAs), silicon carbide (SiC), langasite (LGS), zinc oxide (ZnO), aluminum nitride (AIN), silicon (Si), silicon nitride (Si.sub.3N.sub.4), and lead zirconium titanate (“PZT”); metals or alloys such as aluminum, copper, gold, silver and steel; thermoplastics such as polyesters (e.g., polyethylene terephthalate or polyethylene naphthalates), polyacrylates (e.g., polymethyl methacrylate or “PMMA”), poly(vinyl acetate) (“PVAC”), poly(vinylbutyral) (“PVB)”, poly(ethyl acrylate) (“PEA”), poly(diphenoxyphosphazene) (“PDPP”), polycarbonate (“PC”), polypropylene (“PP”), high density polyethylene (“HDPE”), low density polyethylene (“LDPE”), polysulfone (“PS”), polyether sulfone (“PES”), polyurethane (“PUR”), polyamide (“PA”), polyvinyl chloride (“PVC”), polyvinylidene fluoride (“PVdF”), polystyrene and polyethylene sulfide; and thermoset plastics such as cellulose derivatives, polyimide, polyimide benzoxazole and polybenzoxazole. Recipient substrates can also include paper, nonwovens and foams. Preferably care is taken when selecting the substrate so that there will be an adequate degree of adhesion between the substrate and the material.
As used herein, “curing” means a process of hardening of a material. Typically, curing refers to increasing cross-linking within the material. A “cured” material may be partially cured or fully cured. Materials capable of being cured may include an initiator for curing, such as photo initiators or thermal initiators.
As used herein, “comprising” and “including” are used in an open-ended fashion, and thus should be interpreted to mean “including, but not limited to . . . ”.
Unless otherwise indicated, all numbers expressing feature sizes, amounts, and physical properties used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the foregoing specification and attached claims are approximations that can vary depending upon the desired properties sought to be obtained by those skilled in the art utilizing the teachings disclosed herein.
The recitation of numerical ranges by endpoints includes all numbers subsumed within that range (e.g. 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5) and any range within that range.
As used in this specification and the appended claims, the singular forms “a”, “an”, and “the” encompass embodiments having plural referents, unless the content clearly dictates otherwise. As used in this specification and the appended claims, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
Any material capable of being transferred to and from a feature of a flexographic printing plate may be used in accordance with the teachings presented herein. For example the material may comprise a curable resin.
Illustrative examples of resins that are capable of being polymerized by a free radical mechanism that can be used herein include acrylic-based resins derived from epoxies, polyesters, polyethers, and urethanes, ethylenically unsaturated compounds, aminoplast derivatives having at least one pendant acrylate group, isocyanate derivatives having at least one pendant acrylate group, epoxy resins other than acrylated epoxies, and mixtures and combinations thereof. The term acrylate is used here to encompass both acrylates and methacrylates. U.S. Pat. No. 4,576,850 (Martens) discloses examples of crosslinkable resins that may be used in cube corner element arrays and may be useful as the materials described herein.
Ethylenically unsaturated resins include both monomeric and polymeric compounds that contain atoms of carbon, hydrogen and oxygen, and optionally nitrogen, sulfur, and the halogens may be used herein. Oxygen or nitrogen atoms, or both, are generally present in ether, ester, urethane, amide, and urea groups. Ethylenically unsaturated compounds preferably have a molecular weight of less than about 4,000 and preferably are esters made from the reaction of compounds containing aliphatic monohydroxy groups, aliphatic polyhydroxy groups, and unsaturated carboxylic acids, such as acrylic acid, methacrylic acid, itaconic acid, crotonic acid, iso-crotonic acid, maleic acid, and the like. Such materials are typically readily available commercially and can be readily cross linked.
Some illustrative examples of compounds having an acrylic or methacrylic group that are suitable for use in accordance with the teachings presented herein are listed below:
Illustrative examples of photopolymerization initiators that can be blended with acrylic compounds in the present invention include the following: benzil, methyl o-benzoate, benzoin, benzoin ethyl ether, benzoin isopropyl ether, benzoin isobutyl ether, etc., benzophenone/tertiary amine, acetophenones such as 2,2-diethoxyacetophenone, benzyl methyl ketal, 1-hydroxycyclohexylphenyl ketone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-(4-isopropylphenyl)-2-hydroxy-2-methylpropan-1-one, 2-benzyl--2-N,N-dimethylamino-1-(4-morpholinophenyl)-1-butanone, 2,4,6-trimethylbenzoyl-diphenylphosphine oxide, 2-methyl-1-4(methylthio), phenyl-2-morpholino-1-propanone, bis(2,6-dimethoxybenzoyl)(2,4,4-trimethylpentyl)phosphine oxide, etc. The compounds may be used individually or in combination.
Examples of thermal initiators that may be employed generally include peroxides such as acetyl and benzoyl peroxides. Specific examples of thermal initiators that can be utilized include, but are not limited to, 4,4′-azobis(4-cyanovaleric acid), 1,1′-azobis(cyclohexanecarbonitrile), 2,2′-azobis(2-methylpropionitrile), benzoyl peroxide, 2,2-bis(tert-butylperoxy)butane, 2,5 -bis(tert-butylperoxy)-2,5-dimethylhexane, bis[1-(tert-butylperoxy)-1-methylethyl]benzene, tert-butyl hydroperoxide, tert-butyl peracetate, tert-butyl peroxide, tert-butyl peroxybenzoate, cumene hydroperoxide, dicumyl peroxide, lauroyl peroxide, peracetic acid, and, potassium persulfate. As examples, the photoinitiator may be α-hydroxyketone, phenylglyoxylate, benzildimethyl ketal, α-aminoketone, monoacylphosphine, bisacylphosphine, and mixtures thereof.
Cationically polymerizable materials include but are not limited to materials containing epoxy and vinyl ether functional groups and may be used herein. These systems are photo-initiated by onium salt initiators, such as triarylsulfonium, and diaryliodonium salts.
Materials also comprise a solvent. Any solvent in which the components of the material may be dissolved, dispersed, suspended or the like may be used. The solvent may be an organic compound that does not appreciably participate in the cross-linking reaction, if the material is to be cured, and which exists in a liquid phase at room temperature and 1 atmosphere. The viscosity and surface tension of the solvent are not specifically limited. Examples of suitable solvents include chloroform, acetonitrile, methylethylketone, ethylacetate, and mixtures thereof. Any amount of solvent capable of dissolving, dispersing, suspending, etc. the components of the material may be used. Preferably, a sufficient amount of solvent will be used so that the material can readily be disposed on a donor substrate. Generally, the amount of solvent will range from 60 to 90 wt %, e.g. 70 to 80 wt %, with respect to the total weight of the material.
In addition, at least a portion of the solvent should be actively or passively removable from the material during a flexographic printing process. A reduced solvent material is preferably a flowable material at room temperature or at temperatures at which flexographic printing processes are carried out.
Exemplary methods for printing a material on a recipient substrate using flexographic printing techniques are described below.
Any known or future developed technique suitable for removing solvent from the material may be employed. In some circumstances it may be desirable to allow the solvent to passively evaporate to achieve a reduced solvent material. In other circumstances it may be appropriate to facilitate solvent evaporation through the use of a solvent removal apparatus, such as a microwave or infrared radiation apparatuses to assist in solvent evaporation or dryers.
As shown in
Any amount of solvent may be removed from material to achieve a reduced-solvent material. Preferably a sufficient amount of solvent is removed to enhance the uniformity of transfer of amounts of reduced-solvent material to the feature of the flexographic printing plate. In some cases removing at least 10% of the solvent may be sufficient. In other cases, removing at least 50%, 90%, 95%, 99%, or substantially all of the solvent may be desired. If the reduced-solvent material is to be cured soon after transfer from the feature to a recipient substrate, it will generally be desirable to remove more of the solvent prior to disposing the reduced-solvent material onto the feature than if the reduced-solvent material is to be cured at a time further removed from transfer to the recipient substrate. It will generally be desirable to remove substantially all of the solvent from the material, if the reduced-solvent material is to be cured while it is being transferred from the feature of the printing plate to the recipient substrate, e.g. as described in U.S. Provisional Patent Application Ser. No. 60/865,968, entitled “FLEXOGRAPHIC PRINTING WITH CURING DURING TRANSFER TO SUBSTRATE” to Mikhail Pekurovsky, filed on even date herewith, which application is incorporated herein by reference in its entirety to the extent it does not contradict the disclosure presented herein.
By varying the concentration of solvent in the material or the amount of solvent removed from the material, the thickness of the reduced-solvent material at the point of contact with the feature of the flexographic printing plate can be adjusted to give desirable amounts and placement of the material on the printing feature. For example, if the reduced-solvent material is disposed too thickly on the donor substrate at the point of contact with a feature of the printing plate, the feature may become overloaded and the width of printed material on the recipient substrate will be larger than the lateral dimension of the feature. If the reduced-solvent material is disposed too thinly on the donor substrate at the point of contact with a feature of the printing plate, the feature may not be sufficiently loaded and the quality of the printing may be compromised. The concentration of solvent and solvent removal can readily be adjusted to obtain a desired amount and placement of material on the printing features.
Referring to
Generally, reducing or removing imprints from a donor substrate (170) will comprise removing all or substantially all of the untransferred reduced-solvent material from the donor substrate. Any known or future developed technique may be used to reduce or remove imprints or remove reduced-solvent material from the donor substrate. In an embodiment, a roll may be used to smooth the remaining material on the donor substrate as shown, e.g., in
It will be understood that various steps presented in
The methods described above can be carried out with any suitable flexographic printing system. Exemplary flexographic systems and components thereof suitable for carrying out the methods described above are described below. In describing the exemplary systems, the term material 220 will be used for convenience in describing both material that comprises a fully saturated solution and a reduced solvent material. It should be understood that (i) material 220 when initially disposed onto a donor substrate will comprise a full concentration solvent, (ii) solvent will be removed, actively or passively, from material 220 prior to transfer to a feature of a flexographic printing plate, and (iii) material 220 transferred to the feature refers to reduced-solvent material 220.
Referring to
Flexographic roll 30 is moveable relative to the donor substrate 210 such that material 220 may be transferred from donor substrate 210 to a feature 260 (see, e.g.,
Flexographic roll 230 and backup roll 240, 240A, 240B depicted in
Referring to
Referring to
The system 1000 depicted in
Referring to
For example
Of course it will be understood that the components of the various systems 1000 discussed throughout this disclosure can be interchanged. For example, the system 1000 of
A micro-flexographic printing plate was prepared as described in U.S. Provisional Patent Application Ser. No. 60/865,979, entitled “SOLVENT-ASSISTED EMBOSSING OF FLEXOGRAPHIC PRINTING PLATES” to Mikhail Pekurovsky et al., filed on even date herewith. Briefly, the plate was prepared by taking a polymeric film having a micro-replicated linear prismatic structure (BEF 90/50, commercially available from 3M Co.), referred to as BEF master, depositing a thin layer of methyl ethyl ketone on its structured surface, and then positioning a CYREL® flexographic plate (type TDR B 6.35 mm thick, with removed coversheet, commercially available from DuPont Co.) on the top of the microreplicated surface. After 15 hours, the CYREL® plate was exposed to UV radiation through the attached micro-replicated film in a UV processor equipped with a mercury Fusion UV curing lamp (model MC-6RQN, Rockville, Md., 200 watt/in), run at approximately 5 fpm. The micro-replicated flexographic printing plate was then detached from the BEF master.
The microreplicated flexographic printing plate was then attached to a 12.7 cm-diameter glass cylinder by flexographic mounting tape (type 1120, commercially available from 3M Co.). A thin layer of type 906 hardcoat (33 wt % solids ceramer hardcoat dispersion containing 32 wt % 20 nm SiO2 nano-particles, 8 wt % N,N-dimethyl acrylamid, 8 wt % methacryloxypropyl trimethoxysilane and 52 wt % pentaerythritol tri/tetra acrylate (PETA) in isopropylalcohol (IPA), 3M Co., St. Paul, Minn.) was deposited onto a clean glass slide by dip coating at 0.03 meters per minute from the 906 hardcoat solution in IPA (25 wt % solids), and then drying the glass slide in open air. The flexographic printing plate was then rolled by hand in the layer of hardcoat and then rolled onto a clean 125 micrometer-thick PET poly(ethylene terephtalate) film (available from DuPont Co). The printed PET film was then sent through a UV processor equipped with a mercury Fusion UV curing lamp (model MC-6RQN, Rockville, Md., 200 watt/in, nitrogen purged to 50 ppm O2 content), run at approximately 1.5 meters/min. Lines that were exposed to the UV light were cured and had a width of approximately 2.5 micrometers and were spaced approximately 50 micrometers apart forming a parallel line pattern illustrated with the micrographic image of
A micro-flexographic printing plate was prepared as described in U.S. Provisional Patent Application Ser. No. 60/865,979, entitled “SOLVENT-ASSISTED EMBOSSING OF FLEXOGRAPHIC PRINTING PLATES” to Mikhail Pekurovsky et al., filed on even date herewith. Briefly, the plate was prepared by taking a polymeric film with a micro-replicated cube-corner structure, depositing a small amount of methyl ethyl ketone on the master tool structured surface, and then positioning a CYREL® flexographic plate (type TDR B 6.35 mm thick, with removed cover sheet, available from DuPont Co.) on the top of the master tool microreplicated surface. After 15 hours, the CYREL® plate was exposed to UV radiation through attached microreplicated film in a UV processor (Fusion UV Curing lamp, model MC-6RQN, Rockville, Md., 200 watt/in, mercury lamp, run at approximately 1.5 meters per second) and then the microreplicated flexographic printing plate was detached from the master tool. This microreplicated flexographic printing plate was then attached to a 12.7 cm-diameter glass cylinder by flexographic mounting tape (type 1120, commercially available from 3M Co.). A micrographic image of this microreplicated flexographic printing plate illustrating the features is shown in
A thin layer of 906 hardcoat (described in Example 1) was deposited onto a clean glass slide by dip coating at 0.03 meters per minute from a 906 hardcoat solution in IPA (25 wt % solids), and drying that glass slide in open air. The flexographic printing plate was then rolled by hand in that layer of hardcoat and then rolled onto a clean 125 micrometer PET i.e., poly(ethylene terephtalate) film (available from DuPont Co). This PET film with printed lines was sent through a UV processor (Fusion UV Curing lamp, model MC-6RQN, Rockville, Md., 200 watt/inch, mercury lamp, purged by nitrogen to approximately 50 ppm of oxygen, run at approximately 1.5 meter per minute). The resulting printed lines were approximately 3 micrometers wide and 135 micrometers long forming a triangular pattern as illustrated in the micrographic image shown in
Thus, embodiments of SOLVENT REMOVAL ASSISTED MATERIAL TRANSFER FOR FLEXOGRAPHIC PRINTING are disclosed. One skilled in the art will appreciate that embodiments other than those disclosed are envisioned. The disclosed embodiments are presented for purposes of illustration and not limitation, and the present invention is limited only by the claims that follow.
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/US2007/083563 | 11/5/2007 | WO | 00 | 5/14/2009 |
Number | Date | Country | |
---|---|---|---|
60865976 | Nov 2006 | US |