Classifications

• • 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
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/52—Macromolecular coatings
• • 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
• • 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
  • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
  • C09D175/04—Polyurethanes
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
  • C09J133/04—Homopolymers or copolymers of esters
  • C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
  • C09J133/10—Homopolymers or copolymers of methacrylic acid esters
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
  • C09J133/04—Homopolymers or copolymers of esters
  • C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
  • C09J133/10—Homopolymers or copolymers of methacrylic acid esters
  • C09J133/12—Homopolymers or copolymers of methyl methacrylate
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
  • C09J133/04—Homopolymers or copolymers of esters
  • C09J133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J7/00—Adhesives in the form of films or foils
  • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
  • C09J7/29—Laminated material
• • 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
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/502—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording characterised by structural details, e.g. multilayer materials
  • B41M5/508—Supports
• • 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
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/52—Macromolecular coatings
  • B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
• • 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
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/52—Macromolecular coatings
  • B41M5/5263—Macromolecular coatings characterised by the use of polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • B41M5/5281—Polyurethanes or polyureas
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
  • C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
  • C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
  • C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
  • C08L2666/06—Homopolymers or copolymers of unsaturated hydrocarbons; Derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
  • C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
  • C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
  • C08L2666/20—Macromolecular compounds having nitrogen in the main chain according to C08L75/00 - C08L79/00; Derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
  • C09J2203/334—Applications of adhesives in processes or use of adhesives in the form of films or foils as a label
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J2301/00—Additional features of adhesives in the form of films or foils
  • C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
  • C09J2301/16—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the structure of the carrier layer
  • C09J2301/162—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the structure of the carrier layer the carrier being a laminate constituted by plastic layers only
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J2301/00—Additional features of adhesives in the form of films or foils
  • C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
  • C09J2301/416—Additional features of adhesives in the form of films or foils characterized by the presence of essential components use of irradiation

Definitions

• the present invention relates to an ink receptive layer and an image article imaged with a UN-curable ink.
• Typical promotional window graphics fall into two main areas, adhesive coated vinyl and cling vinyl films.
• Such films are usually screen printed with UN-curable inks.
• the artwork utilizes line colors, which tends to maximize the visual impact of the graphic as compared to 4-color printing.
• the line color printing creates an almost continuous layer of ink on the graphic film. This large amount of ink (up to five layers of UN-cured ink in localized areas of the graphic) significantly decreases the ductile strength of the film, which becomes more brittle and can break or tear more easily as a result of the brittle UN- cured ink layers adhering to the film.
• Imaged cling vinyl films tend to have very good visual presentation when first applied to glass. However, such imaged films tend to lift and bubble over time because of very low peel adhesion to the glass. Adhesive coated vinyl graphic films adhere well to glass. However, such graphic films can tear or break into small pieces during removal due to decreased ductility from the UN-cured ink layers. Such tearing or breakage makes removal of the graphic films more difficult, and increases removal time. In addition, anchorage of the UN-curable ink after cure to the film is important to the initial application of the graphic to a substrate. During application of the graphic to a substrate, stretching (or extension) of the graphic can occur. Current vinyl graphics films have the potential for the ink to flake off at low film extensions, decreasing the visual impact of the graphic.
• One method to alleviate tearing of the film and flaking of the ink is to significantly increase the thickness of the vinyl film.
• the film thickness is increased to, for example, above 6 mils (above about 150 micrometers), to address these issues, the graphic costs become commercially prohibitive.
• polyolefin based graphics films are also used for promotional window graphics. Although these films have improved tear strength after imaging, the adhesion of UN- curable screen print inks to the polyolefin is typically less that that of vinyl, resulting in more pronounced ink flaking. Summary In one aspect, the invention provides an imaged article that comprises A) an image receptive layer bonded to a core layer and B) an image on the image receptive layer, the image comprising a UN-curable or UN-cured ink.
• the image receptive layer comprises a blend of i) a carrier resin comprising modified polyolefin or polyurethane resin, or combinations thereof; and ii) an ink-anchoring resin selected from the group consisting of copolymers of methyl methacrylate with butyl acrylate, butyl methacrylate, isobutyl methacrylate, or isobornyl methacrylate; copolymers of isobutylmethacrylate and butyl methacrylate; polymers of isobutyl methacrylate; copolymers of urethane and acrylate; acrylic polymers, and combinations thereof.
• the invention provides a method of using an imaged graphic article of the invention.
• the method comprises the steps of: providing an imaged graphic article comprising a UN-curable or UN-cured ink, the graphic article comprising a core layer bonded to an image receptive layer, and an adhesive on a surface of the core layer opposite the image receptive layer, the image receptive layer comprising a blend of i) a carrier resin comprising modified polyolefin or polyurethane resin, or combinations thereof; and ii) an ink-anchoring resin selected from the group consisting of copolymers of methyl methacrylate with butyl acrylate, butyl methacrylate, isobutyl methacrylate, or isobornyl methacrylate; copolymers of isobutylmethacrylate and butyl methacrylate; polymers of isobutyl methacrylate; copolymers of urethane and acrylate; acrylic polymers, and combinations thereof, adh
• Figure 1 is a schematic cross-sectional view illustrating an embodiment of the invention including an image receptive layer and a core layer.
• FIG. 2 is a schematic cross-sectional view illustrating an embodiment of the invention including an image receptive layer and a core layer and an optional prime layer.
• the invention provides an image receptor medium comprising a single extrudable image receptive layer on a substrate or core layer.
• the image receptive layer is a layer that is receptive to UN-curable inks and provides excellent adhesion to the cured ink.
• the image receptive layer comprises a blend of a carrier resin and ink- anchoring resin.
• the image receptor medium 10 comprises a core layer 14 having two major surfaces and an image receptive layer 12 in contact and coextruded with the core layer 14 to form the image receptor medium 10.
• an image receptive layer 12 may be extrusion coated or solvent cast directly onto a core layer.
• the carrier resin may be any resin or blend of resins that is compatible with the ink-anchoring resin described below.
• An ink-anchoring resin is compatible with the carrier resin if a film comprising the carrier resin and an ink-anchoring resin can be melt blended and extruded to form a self supporting film or can be coextruded with, or extrusion coated onto, a core layer film as a support.
• the carrier resins are generally olefin-based.
• copolymers comprising the reaction product of olefin monomers and a sufficient amount of at least one polar monomer (modified olefin resins) provide the desired carrier resin.
• modified olefin resins include copolymers of ethylene and vinyl acetate, carbon monoxide, and methyl acrylate; copolymers of acid and/or acrylate modified ethylene and vinyl acetate; and terpolymers of ethylene and any two polar monomers, for example, vinyl acetate and carbon monoxide and combinations thereof.
• thermoplastic polyurethanes and polyether-ester elastomers include urethanes and polyesters such as thermoplastic polyurethanes and polyether-ester elastomers.
• Useful thermoplastic urethane resins include MORTHA ⁇ E P ⁇ 343-200, MORTHANE PN 3429-218, MORTHANE PN 03- 214, and MORTHANE L 425-181 from Rohm and Haas, Philadelphia, PA; ESTANE 58315, ESTANE 58271, and those sold under the trade designation ELASTOLLAN from BF Goodrich, Cleveland, OH; TEXL DP7-3006 and TEXLN DP7-3007 from Bayer Corporation, Pittsburgh, PA; PELLETHANE 2354 and PELLETHANE 2355 from The
• Useful polyether-ester resins include HYTREL G3548L, HYTREL G4078W, and HYTREL G4778 from E.I. DuPont De Nemours, Wilmington, DE.
• Other useful copolyester resins include those available from Eastman Chemical, Kingsport, TN, under the trade designation EASTAR.
• modified olefin resins that are useful as carrier resins include: BYNEL 3101, an acid-acrylate modified ethylene vinyl acetate copolymer; ELVALOY 741, a terpolymer of ethylene/vinyl acetate/carbon monoxide; ELNALOY 4924, a terpolymer of ethylene/vinyl acetate/carbon monoxide; ELNALOY 1218AC, a copolymer of ethylene and methyl acrylate; and FUSABO ⁇ D MG-423D, a modified ethylene/acrylate/carbon monoxide terpolymer; and combinations thereof. All are available from E.I. DuPont De Nemours.
• the carrier resin is present in the image receptive layer at a level of from 50 to 90 weight percent. In other embodiments, the carrier resin is present in the image receptive layer in an amount of from at least about 30 weight percent, at least about 50 weight percent, and least about 70 weight percent.
• useful ink-anchoring resins include (meth) acrylic resins such as PARALOID and ACRYLOID resins from Rohm and Haas.
• Useful (meth) acrylic resins have a Tg of 90 °C or less.
• useful (meth) acrylic resins include copolymers of methyl methacrylate with butyl acrylate, butyl methacrylate, isobutyl methacrylate, or isobornyl methacrylate (for example, PARALOID DM-55, PARALOID B48N, PARALOID B66, ELNACITE 2550); copolymers of isobutylmethacrylate and butyl methacrylate (for example, ELNACITE 2046); isobutyl methacrylate resins (for example, PARALOID B67); and copolymers of urethanes and acrylates such as ⁇ EOCRYL A-612 and ⁇ EOPAC R-9000 aqueous acrylic emulsions from Avecia Ltd.
• the ink-anchoring resin is typically present in the image receptive layers of the invention in an amount of from 10 to 50 weight percent and any fractional or whole weight percent between 10 and 50 weight percent. In other embodiments, the ink- anchoring resin is present in the image receptive layers of the invention in an amount of from 10 and 30, and from 15 to 25 weight percent and any fractional or whole weight percent between 10 and 30 and 15 and 25 weight percent, respectively.
• the image receptive layer is at least 0.1 mils (2.5 micrometers) thick, and in other embodiments, the image receptive layer has a thickness that ranges from 0.7 mils (17.8 micrometers) to 2.0 mils (50.8 micrometers) thick, and may be any whole or fractional thickness in between 0.7 mils (17.8 micrometers) and 2 mils (50.8 micrometers).
• the image receptive layer may include one or more filler materials. Inorganic fillers such as crystalline and amorphous silica, clay particles, aluminum silicate, titanium dioxide and calcium carbonate, and the like are a preferred additive in order to impart one or more of desirable properties, such as, improved dot gain and color density, and improved abrasion resistance.
• the concentration of such fillers in the image receptive layers of the invention typically range from 0.1 weight percent to 25 weight percent by weight. In another embodiment, the concentration of such fillers in the image receptive layers of the invention typically ranges from 0.5 weight percent to 15 weight percent.
• stabilizing chemicals can be added optionally to the primer compositions.
• These stabilizers can be grouped into the following categories: heat stabilizers, UN light stabilizers, and free- radical scavengers.
• Heat stabilizers are commonly used to protect the resulting image graphic against the effects of heat and are commercially available from Witco Corp., Greenwich, CT, under the trade designation MARK N 1923; and Ferro Corp., Polymer Additives Div.,
• Such heat stabilizers can be present in amounts ranging from 0.02 to 0.15 weight percent.
• Ultraviolet-light stabilizers can be present in amounts ranging from 0.1 to 5 weight percent of the total primer or ink.
• Benzophenone type UN-absorbers are commercially available from BASF Corp., Parsippany, ⁇ J, under the trade designation UVL ⁇ OL 400; Cytec Industries, West Patterson, ⁇ J, under the trade designation CYASORB UNI 164; and Ciba Specialty Chemicals, under the trade designations TL UNL 900 and TL UNL ⁇ 1130.
• Free-radical scavengers can be present in an amount from 0.05 to 0.25 weight percent of the total primer composition.
• free-radical scavengers include hindered amine light stabilizer (HALS) compounds, hydroxylamines, sterically hindered phenols, and the like.
• HALS hindered amine light stabilizer
• HALS compounds are commercially available from Ciba Specialty Chemicals, under the trade designations TINUNIN 292 and TINUNIN 123; and Cytec Industries, under the trade designation CYASORB UV3581.
• the image receptive layer is typically substantially free of colorant. However, it may also contain colorants to provide a uniform background colored film.
• a core layer 14 is included in the image receptor medium, for example, to reduce the cost and/or enhance the physical properties of the medium.
• the core layer 14 is most commonly white and opaque for graphic display applications, but could also be transparent, translucent, or colored opaque.
• Core layer 14 can comprise any polymer having desirable physical properties for the intended application. Properties of flexibility or stiffness, durability, tear resistance, conformability to non-uniform surfaces, die cuttability, weatherability, solvent resistance (from solvents in inks), resistance to gasoline and other fuels, heat resistance and elasticity are examples.
• a graphic marking film used in short term outdoor promotional displays typically can withstand outdoor conditions for a period in the range from about 3 months to about one year or more and exhibits tear resistance and durability for easy application and removal.
• the material for the core layer is a resin capable of being extruded or coextruded into a substantially two-dimensional film and exhibits tear resistance.
• suitable materials for the core layer include polyester, polyolefin, polyamide, polycarbonate, polyurethane, polystyrene, acrylic, plasticized polyvinyl chloride, or combinations thereof.
• the core layer may comprise materials that have the same physical properties as described above, but may not be extrudable.
• the core layer comprises a non-plasticized polymer to avoid difficulties with plasticizer migration and staining in the image receptor medium.
• the core layer comprises a polyolefin that is a propylene-ethylene copolymer containing about 6 weight percent ethylene. Resins comprising poly vinylchloride may also be used as the core layer but are not typical since such resins may not provide adequate tear resistance.
• the core layer may also contain other components such as pigments, fillers, ultraviolet stabilizing agents, slip agents, antiblock agents, antistatic agents, and processing aids familiar to those skilled in the art.
• the core layer is commonly white opaque, but may also be transparent, colored opaque, or translucent.
• a typical thickness of the core layer 14 is in the range from 0.5 mils (12.7 micrometers) to 12 mils (305 micrometers). However, the thickness may be outside this range providing the resulting image receptor medium is not too thick to feed into a printer or an image transfer device, that is, any device capable of providing an image-wise layer of UN-curable ink onto the receptive layer.
• a useful thickness is generally determined based on the requirements of the desired application.
• optional prime layer 16 is located on the surface of core layer 14 opposite image receptive layer 12.
• the prime layer is located on the surface of the image receptive layer 12 opposite the outer surface 13.
• the prime layer serves to increase the bond strength between the substrate layer and an adhesive layer 17 if the bond strength is not sufficiently high without the prime layer.
• the presence of an adhesive layer makes the image receptor medium useful as an adhesive backed graphic marking film.
• any adhesive that is particularly suited to the substrate layer and to the selected application can be used.
• Such adhesives are those known in the art and may include aggressively tacky adhesives, pressure sensitive adhesives, repositionable or positionable adhesives, hot melt adhesives, and the like.
• the image receptor media of the invention may also have an optional tie layer (not shown) between image receptive layer 12 and the core layer 14.
• a tie layer is used to improve adherence between the image receptive layer and the core layer.
• Useful tie layers include extrudable resins such as ethylene vinyl acetate resins, and modified ethylene vinyl acetate resins (modified with acid, acrylate, maleic anhydride, individually, or in combinations).
• the tie layer may consist of these materials by themselves or as blends of these resins with the carrier resin.
• Use of tie layer resins is well known in the art and varies depending on the composition of the two layers to be bonded.
• Tie layers for extrusion coating could include the same types of materials listed above and other materials such as polyethyleneimine, which are commonly used to enhance the adhesion of extrusion coated layers. Tie layers can be applied to the core layer or image receptive layer by coextrusion, extrusion coating, laminating, or solvent coating processes.
• the UN-curable screen printable inks useful in combination with the invention include Screen Print Ink Series 9700, available from 3M Company, St. Paul, M ⁇ ; DURACAL and PLASTICAL brand UN-curable inks, available from Sericol Ltd. Kent, England; UV ⁇ -MP UN-curable inks, available from Coates Screen, St. Charles, EL, and 3200 and 3800 series UN-curable inks, available from ⁇ azdar, Shawnee, KS.
• Useful UN- curable inkjet inks are described in U.S. Publication No 2002086914, and PCT Publication Nos. WO 200261002 and WO 200262894.
• the image receptor medium of this invention can be made by a number of methods.
• image receptive layer 12 and optional layers 14 and 16 can be coextruded using any suitable type of coextrusion die and any suitable method of film making such as blown film extrusion or cast film extrusion.
• layer 12 can be extrusion coated onto a substrate or a core layer or other support.
• Adhesive layer 17 may be coextruded with the other layers, transferred to the image receptor medium from a liner, or directly coated onto the image receptor medium in an additional process step.
• the polymeric materials for each layer are chosen to have similar properties such as melt viscosity.
• one or more of the layers may be extruded as a separate sheet and laminated together to form the image receptor medium.
• the finished image receptor medium does not require surface treatment methods such as corona treatment to improve the image receptivity of the image receptor medium for certain applications, as described in the prior art.
• the imaged, polymeric sheets may be a finished product or an intermediate and are useful for a variety of articles including signage and commercial graphics films.
• Signage includes various retroreflective sheeting products for traffic control as well as non- retroreflective signage such as backlit signs.
• the article is suitable for use as roll-up signs, flags, banners, and other articles including other traffic warning items such as roll-up sheeting, cone wrap sheeting, post wrap sheeting, barrel wrap sheeting, license plate sheeting, barricade sheeting, and sign sheeting; vehicle markings and segmented vehicle markings; pavement marking tapes and sheeting; as well as retroreflective tapes.
• the article is also useful in a wide variety of retroreflective safety devices including articles of clothing, construction work zone vests, life jackets, rainwear, logos, patches, promotional items, luggage, briefcases, book bags, backpacks, rafts, canes, umbrellas, animal collars, truck markings, trailer covers, and curtains, etc.
• Commercial graphic films include a variety of advertising, promotional, and corporate identity imaged films.
• the films typically comprise a pressure sensitive adhesive on the non- viewing surface in order that the films can be adhered to a target surface such as an automobile, truck, airplane, billboard, building, awning, window, floor, etc.
• the image receptor medium is screen printed directly with a UN-curable ink, thereby receiving the desired image without the extra image transfer step.
• the techniques and materials for practicing screen-printing are described in U.S. Pat. No. 4,737,224.
• the imaged film is then used as described above.
• the image receptive layer of the present invention is particularly suitable for screen- printing of UN-curable inks because the image receptive layer is extremely tolerant of the effects of UN light used to cure solventless inks used in screen-printing.
• An example of such inks is disclosed in U.S. Pat. No. 5,462,768.
• the image receptor medium is fed into an inkjet printer and printed directly with the desired image.
• the inkjet printer can print using UN-curable piezo inkjet inks.
• Piezo inkjet printers include those made by Idanit
• Example 1 The film used in Example 1 was 102 micrometers (4 mils) in gauge (thickness). The film contained the following layers in order shown in Table 1.
• the film was formed by coextrusion, which may be carried out by known processes. Techniques of coextrusion are found in many polymer processing references, including Progelhof, R.C., and Throne, J.L. "Polymer Engineering Principles", Hanser/Gardner Publications, Inc., Cincinnati, OH, 1993.
• the LLDPE film of Comparative Example 4 is a linear low density polyethylene film made by the same method as that used to make the film of Example 1 (shown in Table 1) except that it consisted of a single layer at 4.0 mils (102 microns) of the core formulation.
• the film described in Table 1 was tested for printing and mechanical properties of the printed samples against some commercially available materials (Cl - C4) shown in Table 2.
• a pressure sensitive adhesive layer on a release liner (adhesive/liner) was laminated to the film samples before printing using a laminating nip.
• the prime layer side of the film of Example 1 was laminated against the pressure sensitive adhesive side of the adhesive/liner.
• Example 1 and Cl were line color printed with UN-cured screen- printing inks using the methods described in U.S. Pat. No. 4,737,224.
• One sample was printed with one layer of ink, a second sample was printed with two layers of ink, and further samples were printed with three, four, and five layers of ink, respectively. This was done for both Example 1 and Cl.
• the print areas were 100 percent fill, that is, a continuous layer or block of ink of the color was printed.
• Printing was carried out using Coates UVN-MP screen print ink (available from Coates Screen), using a 380-mesh screen. After each pass, the freshly printed ink layer was cured at 0.110 J/cm ⁇ for each pass. Each sample was cured between each successive layer of ink. If there were less than five layers of ink, the sample was passed under the UN-cure station a total number of five passes.
• Examples 2 to 5 utilized XP-6427A, a white cast film, commercially available from Pliant Corporation, Schamburg, EL. Coating Composition A
• NEOREZ R600 aliphatic urethane dispersion (800 g) (available from Avecia Ltd.) and NEOCRYL A612 aqueous acrylic emulsion (200 g) (Avecia Ltd.) were blended together in a 4 L container, covered and shaken by hand.
• Deionized water (500 g) was added and mixed, then 500 g of isopropyl alcohol (IP A) was added and mixed.
• IP A isopropyl alcohol
• NEOPAC R9000 aqueous urethane copolymers (40 percent solids) (400 g) (Avecia Ltd.) and NEOCRYL A612 aqueous acrylic emulsion (100 g) were blended together in the same manner as Coating Composition A, but were diluted with 2296 g deionized water and 984 g -PA to yield a final composition which was 5.0 weight percent solids.
• Coating Composition C NEOPAC R9000 aqueous urethane copolymers as obtained.
• NEOPAC R9000 aqueous urethane copolymer dispersion was diluted to 20 weight percent solids with a 50/50 blend of deionized water and D?A.
• the films were coated on their shiny sides with aqueous polyurethane coating formulations on a Hirano Coater (Model M-2001, available from Hirano Tecseed Co. Ltd., Nara, JP) using a ruling mill gravure roll having a volume factor of 36.2 billion cubic micrometers/in ⁇ .
• the coated films were dried by pulling the film through a six-meter long forced air oven set at 85 °C at the film speed given in the roll ratio described below in
• the coated films were laminated with a removable, microsphere based, pressure sensitive acrylate adhesive that was made from a blend of a dispersion of hollow tacky microspheres prepared as described in WO 92/13924, Example 1, and a non spherical acrylate adhesive commercially available from 3M Company, St. Paul MN, under the trade designation FASTBOND 49 at a ratio of 46 to 54.
• This blend had first been coated onto a silicone-coated liner at a wet thickness of 3 mils (0.008 cm), and then dried at 150 °F (66 °C) for ten minutes.
• the film samples were coated with two line colors layers of Coates UNMP and cured as described above.
• the imaged articles were tested for elongation at break and ink flaking as described above. The data are shown in Table 5.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Laminated Bodies (AREA)
• Inks, Pencil-Leads, Or Crayons (AREA)
• Ink Jet (AREA)
• Printing Methods (AREA)
• Ink Jet Recording Methods And Recording Media Thereof (AREA)
• Adhesive Tapes (AREA)
• Photometry And Measurement Of Optical Pulse Characteristics (AREA)

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• 2002
  • 2002-12-23 US US10/328,523 patent/US6857737B2/en not_active Expired - Lifetime
• 2003
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