Nothing Special   »   [go: up one dir, main page]

EP0716633A1 - Ink jet imaging process and recording element - Google Patents

Ink jet imaging process and recording element

Info

Publication number
EP0716633A1
EP0716633A1 EP94927239A EP94927239A EP0716633A1 EP 0716633 A1 EP0716633 A1 EP 0716633A1 EP 94927239 A EP94927239 A EP 94927239A EP 94927239 A EP94927239 A EP 94927239A EP 0716633 A1 EP0716633 A1 EP 0716633A1
Authority
EP
European Patent Office
Prior art keywords
layer
ink
adhesive
substrate
imaged
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.)
Granted
Application number
EP94927239A
Other languages
German (de)
French (fr)
Other versions
EP0716633B1 (en
EP0716633A4 (en
Inventor
Douglas Allan Cahill
Richard Scott Himmelwright
Dene Harvey Taylor
Donald Armand Brault
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Image Products Group LLC
Original Assignee
Rexham Graphics Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US08/115,561 external-priority patent/US5795425A/en
Priority claimed from US08/115,564 external-priority patent/US5766398A/en
Application filed by Rexham Graphics Inc filed Critical Rexham Graphics Inc
Publication of EP0716633A1 publication Critical patent/EP0716633A1/en
Publication of EP0716633A4 publication Critical patent/EP0716633A4/en
Application granted granted Critical
Publication of EP0716633B1 publication Critical patent/EP0716633B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B44DECORATIVE ARTS
    • B44CPRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
    • B44C1/00Processes, not specifically provided for elsewhere, for producing decorative surface effects
    • B44C1/16Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like
    • B44C1/165Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like for decalcomanias; sheet material therefor
    • B44C1/17Dry transfer
    • B44C1/1712Decalcomanias applied under heat and pressure, e.g. provided with a heat activable adhesive
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/502Recording 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
    • B41M5/506Intermediate layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M7/00After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
    • B41M7/0027After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using protective coatings or layers by lamination or by fusion of the coatings or layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5236Macromolecular coatings characterised by the use of natural gums, of proteins, e.g. gelatins, or of macromolecular carbohydrates, e.g. cellulose
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5254Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5263Macromolecular coatings characterised by the use of polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • B41M5/5272Polyesters; Polycarbonates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5263Macromolecular coatings characterised by the use of polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • B41M5/5281Polyurethanes or polyureas

Definitions

  • This invention relates to ink jet printing processes for making images, and particularly, color images. More particularly, this invention relates to ink jet printing processes and the elements used therein for the production and protection of large size, full color images.
  • ink jet printing processes in the manufacture of multicolor images is well known in the art.
  • ink droplets are emitted from a nozzle and deposited on substrates, such as paper, to form an image.
  • substrates such as paper
  • rapid absorption of the ink into the substrate is required, but at the same time the ink colorant must be retained at or near the surface of the substrate with lateral ink migration limited to the resolution of the printer.
  • Ink jet printing and its use in making full color images is reviewed in general by Werner E.
  • the substrate e.g., paper
  • the substrate is coated with a formulation to meet the requirements discussed supra.
  • paper stock is extensively used as the substrate for ink jet printing, many other materials are used including plastic films and sheets, and the like.
  • transparencies typically a coated transparent plastic film or sheet is used as the substrate. Since aqueous based inks are the common type of ink used in ink jet printing processes, substrate coating formulations typically are hydrophilic and contain appropriate absorptive materials.
  • ink jet printing processes, inks and substrates are capable of producing high quality four color images in sizes ranging from office copy up to sizes useful for posters, displays and billboards.
  • application of ink jet printing has been limited largely to such uses as office copy and the like where environmental and abrasion damage to the finished ink image is unlikely.
  • the water sensitive ink jet image and underlying substrate must be protected from rain, sunlight, and other environmental contaminants and should likewise be protected from abrasion and graffiti to provide adequate useful life to the image displayed.
  • an image protective film and its method of use is disclosed in Yoshida, U.S. Patent 5,217,773; the film comprises a base layer, a release layer formed of a resin having no compatibility with the base layer and an adhesive layer formed of a thermoadhesive resin.
  • the film is superposed on an image surface of an object article such that the adhesive layer comes in contact with the image surface and thereafter heated.
  • the base layer is separated from the object article and the adhesive layer and the release layer remain on the object article to form a protective layer.
  • a substrate comprising: a) a support; and b) a first adhesive layer on a first surface of said support, by contacting said first surface of said substrate to said imaged ink receptive layer, and,
  • the first adhesive layer of the substrate is omitted and the ink receptive layer includes an adhesive which is activated to permanently adhere the imaged ink receptive layer to the substrate.
  • the substrate further comprises: c) a second adhesive layer on a second surface of said support opposite said first surface; and optionally, d) a removable cover sheet temporarily adhered to the second adhesive layer; and in performing step (B) the substrate is oriented so that the surface of the substrate bearing the second adhesive layer is away from the imaged ink receptive layer and either before or after step (C) , there is performed the additional step: D) removing the removable cover sheet, if present, from the adhesive layer and adhering the adhesive layer of the imaged laminate to a second substrate to form a mounted, imaged laminate.
  • the image transparent, ink receptive layer is receptive to aqueous ink jet inks and comprises a hydrophilic resin material and, optionally, an adhesive material.
  • Figure 1 is a cross section view illustrating details of the ink deposition step of the process of this invention and an ink receptive element used therein.
  • Figure 2 is a cross section view illustrating details of the imaged ink receptive element and the substrate.
  • Figures 3a and 3b are cross section views illustrating subsequent process steps of this invention using the element of figure 2.
  • Figure 4 is a cross section view illustrating details of an alternate embodiment of the imaged ink receptive element and the substrate.
  • Figures 5a and 5b are cross section views illustrating subsequent process steps of this invention using the element of figure 4.
  • the first process step (A) comprises imagewise depositing one or more ink images on an ink receptor element.
  • an ink jet device (11) traversing in a direction (19) across an ink receptor element, imagewise deposits ink droplets (17) on an image transparent, ink receptive layer (16) to form an imaged ink receptive layer (18).
  • the imaged ink receptor element (10) which is formed comprises; a temporary carrier layer (12), an image transparent, protective layer (14), and an image transparent imaged ink receptive layer (18) .
  • the ink jet device (11) which is used to generate an image on the imaged ink receptive layer (18) may be any of the conventional ink jet printers used to print a single color or a full color image as disclosed by Werner E. Haas in "Non- Impact Printing Technologies": Chapter 13, pages 379-384, supra. Additional ink jet devices include Hewlett Packard Desk Jet 500 and 500C printers; IBM Lexmark ® ink jet printers; Cannon Bubblejet ® printers; ENCAD Computer Corporation Novajet ® printers; and the like.
  • an imaged ink receptive layer (18) e.g., a four color subtractive color image consisting of yellow, magenta, cyan and black images in register.
  • the ink image typically is printed on the ink receptive layer (16) as a reverse or mirror image so that the completed protected ink image will possess correct orientation when applied to an opaque substrate.
  • the inks used in the ink imaging process of this invention are well known for this purpose.
  • the ink compositions used typically are liquid compositions comprising a solvent or carrier liquid, dyes or pigments, humectant, organic solvents, detergents, thickeners, preservatives, and the like.
  • the solvent or carrier liquid typically is water, although ink in which organic materials such as polyhydric alcohols as the predominant solvent or carrier also are used.
  • the dyes used in such compositions are typically water-soluble direct or acid type dyes.
  • Such liquid ink compositions have been extensively described in the prior art, e.g. , such as disclosed by P. Gender in "Materials Aspects For High Quality Color Thermal Ink Jet Printing" IS&T's 46th Annual Conference (1993), pages 175-177.
  • the imaged receptor element (10) is oriented to a substrate (20), comprising a support (22) and a first adhesive layer (24) applied to a first surface of the support, so that the surface of the adhesive layer (24) faces the surface of the imaged ink receptive layer (18)
  • the temporary carrier layer (12) of the ink receptor element (10) functions as a temporary support to the superposed layers during the process steps of this invention and may be any web or sheet material possessing suitable flexibility, dimensional stability and adherence properties to the protective layer (14).
  • the web or sheet material is a flexible polymeric film, e.g.
  • a foraminous material e.g., such as a paper sheet and the like.
  • the web or sheet may also be surface treated or coated with a material to enhance desired release characteristics, e.g., such as treatment with a silicone release agent and the like.
  • the protective layer (14) of the ink receptor element (10) is a polymeric film material which is resistant to scratching, abrasions and the like, and to environmental components and contaminants.
  • the protective layer (14) is permanently adhered to the image transparent, ink receptive layer (16) while being only temporarily adhered to the temporary carrier layer (12).
  • the protective layer (14) is visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region.
  • Polymeric materials which are useful in making this layer include polyvinyl chloride; polyvinylidene chloride; fluorinated polymers and copolymers; polyvinyl butyral; cellulose acetate propionate; cellulose acetate butyrate; polyesters; acrylics; fluorinated polymers; polyurethanes; styrene copolymers, e.g., such as styrene acrylonitrile; and combinations thereof.
  • This layer may contain components which strongly absorb ultraviolet radiation thereby reducing damage to underlying images by ambient ultraviolet light, e.g., such as 2-hydroxy-benzophenones; oxalanilides; aryl esters and the like; hindered amine light stabilizers, such as bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate and the like; and combinations thereof.
  • This layer may also contain components which provide protection from biological attack, such as, fungicides and bactericides, and the like.
  • the protective layer (14) may be provided with a matt surface. This matt surface can be obtained by including in the layer particles sufficiently large to give surface irregularities to the layer, or may be imparted or embossed by the surface characteristics of the temporary carrier layer (12). Particles of average diameter in the range of about 1 ⁇ m to about 15 ⁇ m are suitable.
  • the protective layer also may be provided with a graffiti-proof surface, typically, a perfluorinated polymer surface.
  • the protective layer (14) typically has a thickness in the range of about 0.5 ⁇ m to about 20 ⁇ m and preferably in the range of about 3 ⁇ m to about 10 ⁇ m. Such layers typically will withstand scribing with the point of a 4H pencil without breakthrough.
  • the image transparent, ink receptive layer (16) of the ink receptor element (10), is permanently adhered to the protective layer (14), and is a hydrophilic, aqueous ink sorptive, coating material.
  • the ink receptive layer (16) is visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region.
  • the visible spectral region of the ink receptive layer (16) typically is matched to that of the protective layer (14).
  • the image transparent, ink receptive layer (16) may be prepared from a wide variety of hydrophilic, aqueous ink sorptive, coating materials.
  • the ink receptive layer (16) typically is formulated to provide suitable ink receptivity tuned for a particular ink jet device (11) and related ink (17) used therein.
  • suitable formulations for the ink receptive layer (16) are disclosed in Desjarlais, U.S. Patent 4,775,594; Light, U.S. Patent 5,126,195; and Kruse, U.S. Patent 5,198,306.
  • the ink receptive layer (16) typically is comprised of at least one hydrophilic polymer or resin which also may be water soluble.
  • Suitable hydrophilic polymers or resins include polyvinyl alcohols, including substituted polyvinyl alcohols; polyvinyl pyrrolidones, including substituted polyvinyl pyrrolidones; vinyl pyrrolidone/vinyl acetate copolymer; vinyl acetate/acrylic copolymers; acrylic acid polymers and copolymers; acryla ide polymers and copolymers; cellulosic polymers and copolymers; styrene copolymers of allyl alcohol, acrylic acid, malaeic acid, esters or anhydride, and the like; alkylene oxide polymers and copolymers; gelatins and modified gelatins; polysaccharides; and the like.
  • Preferred hydrophilic polymers include polyvinyl pyrrolidone; substituted polyvinyl pyrrolidone; polyvinyl alcohol; substituted polyvinyl alcohol; vinyl pyrrolidone/vinyl acetate copolymer; vinyl acetate/acrylic copolymer; polyacrylic acid; polyacrylamides; hydroxyethylcellulose; carboxyethylcellulose; gelatin; and polysaccharides.
  • the ink receptive layer (16) may also contain other water insoluble or hydrophobic polymers or resins to impart a suitable degree of hydrophilicity and/or other desirable physical and chemical characteristics.
  • Suitable polymers or resins of this class include polymers and copolymers of styrene, acrylics, urethanes, and the like.
  • Preferred polymers and resins of this type include a styrenated acrylic copolymer; styrene/allyl alcohol copolymer; nitrocellulose; carboxylated resin; polyester resin; polyurethane resin; polyketone resin; polyvinyl butyral resin; or mixtures thereof.
  • the ink receptive layer (16) typically contains other added components such as a dye mordant, a surfactant, particulate materials, a colorant, an ultraviolet absorbing material, an organic acid, an optical brightener, and the like.
  • Dye mordants which may be used to fix the printed ink to the ink receptive layer (16) may be any conventional dye mordant, e.g. such as polymeric quaternary ammonium salts, polyvinyl pyrrolidone, and the like.
  • Surfactants which are used as coating aids for the ink receptive layer (16) may be any nonionic, anionic, or cationic surfactant. Particularly useful, are fluorosurfactants, alkylphenoxypolyglycidols, and the like.
  • the ink receptive layer may also contain particulate material.
  • Suitable particulate material includes inorganic particles such as silicas, chalk, calcium carbonate, magnesium carbonate, kaolin, calcined clay, pyrophylite, bentonite, zeolite, talc, synthetic aluminum and calcium silicates, diatomatious earth, anhydrous silicic acid powder, aluminum hydroxide, barite, barium sulfate, gypsum, calcium sulfate, and the like; and organic particles such as polymeric beads including beads of polymethylmethacrylate, copoly(methylmethacrylate/divinylbenzene) , polystyrene, copoly(vinyltoluene/t-butylstyrene/methacrylic acid) , polyethylene, and the like
  • the ink receptive layer (16) may also contain a colorant, e.g., a dye or pigment, provided the layer is visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region.
  • This layer may contain components which strongly absorb ultraviolet radiation thereby reducing damage to underlying images by ambient ultraviolet light, e.g., such as 2-hydroxybenzophenones; oxalanilides; aryl esters and the like; hindered amine light stabilizers, such as bis(2,2,6,6- tetramethyl-4-piperidinyl) sebacate and the like; and combinations thereof.
  • Organic acids which are used to adjust the pH and hydrophilicity in the ink receptive layer (16) typically are non-volatile organic acids such as a alkoxy acetic acid, a glycolic acid, a dibasic carboxylic acid and half esters thereof, a tribasic carboxylic acid and partial esters thereof, aromatic sulfonic acids, and mixtures thereof.
  • Preferred organic acids include glycolic acid, methoxy acetic acid, citric acid, malonic acid, tartaric acid, malic acid, aleic acid, fumaric acid, itaconic acid, succinic acid, oxalic acid, 5-sulfo-salicylic acid, p-toluenesulphonic acid, and mixtures thereof.
  • Optical brighteners which may be used to enhance the visual appearance of the imaged layer may be any conventional, compatible optical brightener, e.g., such as optical brighteners marketed by Ciba-Geigy under the trademark of Tinopal ® .
  • the first adhesive layer (24) of the substrate (20), functions to permanently adhere the imaged ink receptive layer (18) and the protective layer (14) of the imaged receptor element (10), to the substrate during the process of this invention.
  • the adhesive layer (24) may be chosen from a variety of conventional adhesive materials, e.g., such as thermally activated, pressure sensitive, photo-activated, or contact adhesives and the like.
  • the adhesive material will be a thermally activated adhesive material comprised of thermoplastic polyurethanes; polycaprolactone; acrylic copolymers; and combinations thereof.
  • thermally activated adhesive materials include Morthane ® CA- 116 urethane resin (a product of Morton International); Tone ® Polymer P767E biodegradable plastic resin (a product of Union Carbide); Elvax ® 240 Ethylene vinyl acetate (a product of Dupont Chemicals); and the like.
  • the support (22) of the substrate (20) typically functions as the final support for the protected imaged ink receptive layer (18) formed during the process steps of this invention.
  • the support (22) may be any surface upon which an ink jet image is desired. Typically, it is a web or sheet material possessing dimensional stability and adherence properties through the adhesive layer (24) to the imaged ink receptive layer (18) of the imaged ink receptor element (10).
  • the web or sheet material may be a flexible polymeric film, e.g., such as polyethylene terephthalate film and the like; a foraminous material, e.g., such as a paper sheet, textile fabrics, and the like; metal films or webs, e.g., such as aluminum, steel, tin-plate, and the like; or any composites or laminates thereof.
  • the support (22) may be a rigid or semi ⁇ rigid sheeting or plate, e.g., such as sheeting or plates of metal, glass, ceramic, plastic, cardboard, or any composites or laminates thereof.
  • the support (22) may vary in size from that of a photographic print, e.g., having an area of about 30 cm 2 or less, to that of vehicle sign or billboards, e.g., having an area of about 70 m 2 or greater. Since the thin protective (14) and ink receptive (16) layers are highly compliant, the support (22) also may vary in shape and surface topography, e.g., spherical, embossed, etc. When a transparency is to be produced by the process of this invention, the support (22) and first adhesive layer (24) are visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region.
  • This layer may also contain components which strongly absorb ultraviolet radiation thereby reducing damage to underlying images by ambient ultraviolet light, e.g., such as 2-hydroxybenzophenones; oxalanilides; aryl esters and the like; hindered amine light stabilizers, such as bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate and the like; and combinations thereof.
  • the web or sheet may also be surface treated or coated with a material to enhance desired surface characteristics, e.g. sub-coatings, electric discharge treatment, and the like.
  • the imaged ink receptor element (10) can be applied to most solids or foraminous materials, e.g., adhesive backed vinyl, static cling vinyl, and polyethylene terephthlate films; steel, glass, ceramic, and wood sheets and objects.
  • the substrate (20) may further have a second adhesive layer adhered to a second surface of the support (22) opposite the first surface, e.g., the reverse side; and optionally a removable cover sheet may be temporarily adhered to the second adhesive layer.
  • the adhesive material of the second adhesive layer may be any contact, thermal or pressure sensitive adhesive, such as described supra, and may be an integral part of the substrate (20) or it may be applied just prior to a mounting step.
  • a removable cover sheet is temporarily adhered to the adhesive surface(s) of the substrate (20) to protect against damage during storage or preliminary handling.
  • the removable cover sheet may be any conventional release cover sheet.
  • the ink imaging process of this invention comprises three process steps of which the initial process step (A) of producing an imaged receptor element (10) has been described, supra, by reference to Figure 1. The remaining steps of the process will now be described by reference to Figures 3a and 3b.
  • the second process step (B) comprises applying to the imaged ink receptive layer (18) of the ink receptor element (10), the surface of the first adhesive layer (24) of the substrate (20) .
  • the first adhesive layer (24) is contacted and permanently adhered to the imaged ink receptive layer (18) using an applied pressure (31) to the surfaces of the temporary carrier layer (12) and the support (22) to form an imaged laminate (30).
  • the applied pressure (31) must be sufficient to activate the adhesive to form a permanent bond between the layers.
  • the adhesive substrate (20) is typically applied to the imaged ink receptive layer (18) under an applied pressure (31) of atmospheric pressure or greater.
  • the applied pressure (31) may be about 0.07 kg/cm 2 (1 p.s.i.) to about 7 kg/cm 2 (100 p.s.i.) or greater.
  • applied pressure is intended to mean the absolute pressure which is applied to a unit area of the surface as conventionally derived from the geometry of the pressure means, e.g., the geometry of the laminating nip, in combination with a measurement means, e.g., a calibrated gauge pressure.
  • Suitable means that may be used to apply pressure include platen presses; counterpoised, double roll, laminating devices; vacuum laminating devices; scanning, single roll, laminating devices; hand-held, rollers and squeegees; and the like.
  • roll laminating devices are preferred since they readily minimize air entrapment between the adhesive layer (24) and the imaged ink receptive layer (18) during the application process step.
  • Vacuum may be applied with such devices to further eliminate air entrapment.
  • the adhesive layer (24) is a thermally activated adhesive. In this instance, heat is typically applied to the adhesive layer (24) prior to and/or concurrently with the application of the applied pressure (31). While the temperature used to activate the adhesive depends on the nature of the material, the adhesive substrate (20) is applied to the imaged ink receptive layer (18) at a temperature of about 80°C or greater and preferably about
  • the adhesive substrate (20) may be heated prior to its application by radiant or contact heaters and then applied while hot to the imaged ink receptive layer (18).
  • the pressure means itself may also function as a heater, e.g. , such as a hot roll laminator, or both prior and concurrent heating may be used in combination.
  • the adhesive layer (24) may also be a photo-activated adhesive.
  • the adhesive layer (24) typically is irradiated with actinic radiation either concurrently with or subsequent to the application of the applied pressure (31).
  • the support (22) and/or any intervening layer should be sufficiently transparent to the actinic radiation which activates the photo adhesive.
  • the applied pressure (31) may be just sufficient to bring the surface of the adhesive layer (24) into intimate contact with the surface of the imaged ink receptive layer (18).
  • the third process step (C) comprises removing the temporary carrier layer (12) from the surface of the protective layer (14) of the imaged laminate (30).
  • the temporary carrier layer (12) is peeled, using a peel force (41), from the surface of the protective layer (14) to form the completed protected ink image element (40).
  • the temporary carrier layer (12) is peeled with a peel force (41) directed at an angle of 90° or more from the surface of the protective layer (14).
  • the peel rate and the peel force (41) are not critical and preferred values will depend on the nature of the protective and carrier materials.
  • the temperature at which the temporary carrier layer (12) is peeled form the protective layer (14) will depend on the nature of the substrate, adhesive, protective and carrier materials used in the imaged laminate (30).
  • the temporary carrier layer (12) may be peeled at room temperature or, alternatively, the imaged laminate (30) may be heated to facilitate removal of the temporary carrier layer (12).
  • a thermally activated adhesive material is used to form the imaged laminate (30)
  • the temporary carrier layer (12) can be removed immediately after formation of the imaged laminate (30) (i.e., while still in a heated state from the application process step (B)) without delamination of the thermal first adhesive layer (24) or any of the other component layers.
  • the term "immediately” is intended to mean a time span of about 1 minute or less and preferably between about 1 second and about 20 seconds.
  • the laminate when a thermally activated adhesive material is used to form the imaged laminate (30), the laminate may be cooled and stored before removal of the temporary carrier layer (12).
  • the temporary carrier layer (12) can be removed at room temperature from the imaged laminate (30) without delamination of the first adhesive layer (24) or any of the other component layers.
  • the imaged laminate (30) may be reheated prior to removal of the temporary carrier layer (12).
  • the laminate typically is reheated to a temperature which is within about ⁇ 5°C of the temperature used to form the element in process step (B) .
  • the temporary carrier layer (12) may be kept adhered to the imaged laminate (30) during its intermediate storage and handling, and then removed just prior to use.
  • the adhesive substrate (20) further comprises a second adhesive layer adhered to a second surface of the support (22) opposite the first surface; and optionally, there is a removable cover sheet temporarily adhered to the second adhesive layer.
  • the process further comprises; either before or after step (C) , the added step (D) of removing the removable cover sheet, if present, from the second adhesive layer and adhering the second adhesive layer of the protected ink image element (40) to a second substrate to form a mounted, imaged laminate.
  • step (C) the added step of removing the removable cover sheet, if present, from the second adhesive layer and adhering the second adhesive layer of the protected ink image element (40) to a second substrate to form a mounted, imaged laminate.
  • This embodiment is particularly useful for preparing component protected image "tiles" and then mounting each tile to form a composite display image such as on a billboard or the like.
  • the mounting adhesive may be either permanent or temporary.
  • Ink receptor element (110) includes a temporary carrier layer 12 and a protective layer 14 as herein above described.
  • An image transparent, adhesive, ink receptive layer (116) is permanently adhered to the image transparent, protective layer (14), and provides a dual function of ink receptivity as well as an adhesive to the ink receptor element (110).
  • the material of the image transparent, adhesive, ink receptive layer (116) is a hydrophilic, aqueous ink sorptive, coating material as well as an adhesive which, when activated, functions to adhere the protected image to the substrate (122).
  • the adhesive, ink receptive layer (116) may be a blend of the necessary materials in a single layer, or it may be a composite of two or more individual layers wherein one layer would contain the major character of the ink receptive material and the other would contain the major character of an adhesive material and in part a shared character of the ink receptive material.
  • the adhesive, ink receptive layer (116) is visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region.
  • the visible spectral region of the adhesive, ink receptive layer (116) typically is matched to that of the protective layer (14) as stated earlier.
  • the image transparent, adhesive, ink receptive layer (116) may be prepared from a wide variety of hydrophilic, aqueous ink sorptive, coating materials again as herein above described.
  • the adhesive material of the image transparent, adhesive, ink receptive layer (116), becomes imaged layer (118) and functions to permanently adhere itself and protective layer (14) of the imaged receptor element (110), to substrate (122) during the process of this invention.
  • the adhesive material may be chosen from a variety of conventional adhesive materials, e.g., such as thermally activated, pressure sensitive, photo activated, or contact adhesives and the like, provided it is compatible with the components of the ink receptive material and that it contributes, at least in part, to ink receptivity.
  • compatible is intended to mean that the adhesive material may be dispersed within the image transparent, adhesive, ink receptive layer (16) without substantially altering the image transparency or ink receptivity of the layer.
  • the adhesive material will be a thermally activated, hydrophilic, adhesive material comprised of thermoplastic polyurethanes; polycaprolactone; acrylic copolymers; and combinations thereof.
  • thermally activated adhesive materials include Rovace ® HP-2931 vinyl acetate/acrylic copolymer (a product of Rohm & Haas Company); Morthane ® CA- 116 urethane resin (a product of Morton International); Tone ® Polymer P767E biodegradable plastic resin (a product of Union Carbide); Elvax ® 240 Ethylene vinyl acetate (a product of Dupont Chemicals); and the like.
  • preferred adhesive materials are vinyl acetate/acrylic copolymers.
  • preferred adhesive materials are polycaprolactones.
  • the layer typically has a thickness in the range of about 0.5 ⁇ m to about 10 ⁇ m.
  • the ink imaging process of this invention comprises three process steps of which the initial process step (A) of producing an imaged receptor element (110) is the same as was described above by reference to Figure 1. The remaining steps of the process may be described by reference to Figures 5a and 5b.
  • the second process step (B) comprises applying to the imaged layer (118) of the imaged receptor element (110), the surface of the substrate (122).
  • the substrate (122) is contacted and adhered to the imaged ink receptive layer (118) using an applied pressure (131) to the surfaces of the temporary carrier layer (12) and the substrate (122) to activate the adhesive and form an imaged laminate (130).
  • the application and adhering steps used are similar to the steps disclosed above in describing the process wherein the element used had no adhesive in the ink receptive layer. When only a pressure sensitive adhesive is used, the applied pressure (131) must be sufficient to activate the adhesive to form a permanent bond between the layers.
  • the third process step (C) again comprises removing the temporary carrier layer (12) from the surface of the protective layer (14) of the imaged laminate (130).
  • the temporary carrier layer (12) is peeled, using a peel force (41), from the surface of the protective layer (14) to form the completed protected element (140).
  • the substrate (122) may again further comprise an second adhesive layer adhered to a surface thereof and, optionally, a removable cover sheet temporarily adhered to the second adhesive layer.
  • the process further comprises; either before or after step (C) , the added step (D) of removing the removable cover sheet, if present, from the adhesive layer and adhering the adhesive layer of the protected ink image element (140) to a second substrate to form a mounted, imaged laminate.
  • Another embodiment of this invention comprises an added step wherein after step (C) , the image transparent, protective layer along with the image transparent, adhesive, imaged ink receptive layer are removed intact from the substrate.
  • the image transparent, protective layer along with the image transparent, adhesive, imaged ink receptive layer are removed from the substrate, they may be reapplied to the same substrate or to a second substrate.
  • These added steps allow for the complete removal of the adhered layers after a period of use, e.g., removal of a promotional display from a window.
  • the adhered layers may be partially or totally removed, realigned, and then reapplied to the substrate or another substrate, e.g., for display in another window.
  • Example 1 An ink receptor element was prepared as follows: An abrasion resistant coating solution was prepared from the following ingredients.
  • NeoRez ® R-9679 1) polyurethane 90.0 Tinuvin ® 1130 ⁇ ) UV absorber 5.0 Ethanol 5 . 0
  • NeoRez ® R-9679 is an aliphatic aqueous colloidal dispersion of a urethane polymer containing 37% by weight solids (specific gravity of solids is 1.16 and acid number of resin solids is 17.0), and is a product of Zeneca Resins, Inc., Wilmington, Massachusetts.
  • (2) - Tinuvin ® 1130 UV absorber a product of Ciba-Geigy, is the reaction product of polyethylene glycol 300 and the methyl ester of beta-(3-(2h-benzotriazole-2-yl)-4- hydroxy-5-tert-butylphenyl)propionic acid.
  • the Tinuvin ® 1130 was dissolved in the ethanol to form a 50% by weight solution.
  • the Tinuvin ® solution was stirred into the NeoRez ® R-9679 aqueous dispersion in a Lightnin ® mixer at slow speed and mixed for ten minutes.
  • the resulting dispersion was then coated on a 0.10 mm (-0.004 inch) thick, untreated, polyethylene terephthlate film (the temporary carrier layer) using a #16 meyer rod and dried at 240°F (115°C) for two minutes to form the image transparent, protective layer having a dry coating thickness of 3.6 ⁇ m.
  • the Tinuvin ® 1130 UV absorber in the protective layer blocks about 90% of the incident UV radiation having a wavelength between 310 and 380 nm.
  • An ink receptive coating solution was prepared from the following ingredients:
  • Amorphous silica (ave. particle size 15 ⁇ m) ⁇ 5) 0.067 Zonyl ® FSJ (6) fluorosurfactant 0.023
  • - Joncryl ® 61LV acrylic resin solution is, by weight, 35% Joncryl ® 678 acrylic resin, 51% water, 5% isopropanol, 1.5% ethylene glycol, and 7.5% Ammonia (28%); the resin has an acid number of 70 and a Tg of 95°C; and is a product of S.C. Johnson & Son, Inc., Racine, Wisconsin.
  • - PVP K-90 is polyvinylpyrrolidone which has a viscosity average molecular weight of 700,000 and is a product of GAF Chemicals Corporation, Wayne, New Jersey.
  • (5) - Amorphous silica is Syloid ® 620 and is a product of Davison Chemical Division of W.R. Grace & Co., Baltimore, Maryland.
  • (6) - Zonyl ® FSJ is an anionic fluorosurfactant and is a product of E.I. du Pont de Nemours & Co., Wilmington Delaware.
  • An adhesive substrate was made as follows: An adhesive layer coating solution was prepared from the following ingredients.
  • Amorphous silica (ave. particle size 3 ⁇ m) 0.04
  • Morton-Thiokol is a hydroxyl terminated polyurethane elastomer.
  • the coating solution was made by mixing the methyl ethyl ketone, toluene and urethane resin for 30 minutes with a high speed Lightnin ® mixer. Amorphous silica was then added and mixed for 5 minutes. The solution was coated onto a sheet of 0.0055 inch ( ⁇ 0.14 mm) thick static cling vinyl coated with an ink receptive layer and backed with a 10 pt. paper liner (Flexmark ® CV600 W, manufactured by Flexcon Co., Inc.) using a #12 meyer rod and dried at 240°F (115°C) for two minutes to give a dry coating thickness of 2.0 ⁇ m to form the adhesive layer of the adhesive substrate.
  • a 10 pt. paper liner Felexmark ® CV600 W, manufactured by Flexcon Co., Inc.
  • substrates were prepared in the same manner except the substrates were an adhesively backed sheet of 0.004 inch ( ⁇ 0.1 mm) thick untreated cast vinyl polymer having a removable release liner; a sheet of Rexcal ® 4000-000 white cast vinyl sheet (a product of Rexham Branded Products, Lancaster, South Carolina); a sheet of TYPAR ® spunbonded polypropylene fabric with an acrylic primed surface (a product of Eastern Banner Supply, Moorsesville, Indiana; and a corrugated cardboard paper product. Five 8.5 inch x 11 inch ( 21.6 cm x 27.9 cm) sheets were cut from the ink receptor element prepared supra.
  • a four color image was printed on the ink receptive layer of each sheet using an IBM Lexmark ® ink jet printer using the manufacturer's recommended inks and printing conditions. RH was maintained between 50% and 70%, and temperature was maintained between 65°F ( ⁇ 18.3°C) and 75°F ( ⁇ 23.8°C).
  • the laminating step was performed by first laying each adhesive substrate in such a way that the adhesive layer of the adhesive substrate and the ink imaged layer of each imaged receptor element were contacting each other. Each composite was then passed through the hot nip of an IT 6000 hot roll laminator at a speed of 2 feet/minute ( ⁇ 1.02 cm/second), at a temperature of 270°F ( ⁇ 132°C) and at a pressure of 100 psi ( ⁇ 7.0 kg/cm 2 ). As each laminated element exited from the hot nip, the polyethylene terephthlate, temporary carrier layer contiguous to the protective layer was stripped therefrom to form a protected ink image on each of the five substrates. The surface of each protected ink image produced could withstand scribing with a 4H pencil with no removal of the protective layer or image.
  • the protected ink image on the static cling vinyl can be used as a removable decal on a substrate, e.g., a window.
  • the protected ink image on the adhesive backed vinyl can be mounted by the adhesive backing to the surface of a substrate to form a mounted protected image, e.g., a poster, billboard, sign, and the like.
  • the protected ink image on the cast white vinyl sheet can be used as a back lighted display.
  • the protected ink image on the spunbonded polypropylene fabric can be used as a banner.
  • the protected ink image on the corrugated cardboard can be used in product packaging.
  • Example 2 An ink receptor element was prepared as described in Example 1 except that the ink receptive coating solution was prepared from the following ingredients: Ingredient Parts By Weight
  • - Polyvinyl alcohol is GOHSENAL ® T-330H a special grade of Polyvinyl alcohol wherein a 4% water solution at 20°C has a viscosity of 27-32 cps determined by the Hoeppler falling ball method; a hydrolysis of 99-100 mol % (dry basis); and a pH of 6-8.
  • (9) - Amorphous silica is IMSIL ® A-10 and is a product of Illinois Minerals Co., Cairo, Illinois.
  • (10) - Amorphous silica is Hi-Sil ® T-600 and is a product of PPG Industries.
  • An adhesive substrate was made as described in Example 1 except that the substrate was a sheet of cast coated 0.004 inch ( ⁇ 0.1 mm) thick adhesive backed vinyl sheet (Rexcal ® 4000-000).
  • a four color image was printed on the ink receptive layer of the ink receptor element using an IBM Lexmark ® ink jet printer using the manufacturer's recommended inks and printing conditions. RH was maintained between 50% and 70%, and temperature was maintained between 65°F ( ⁇ 18.3°C) and 75°F ( ⁇ 23.8°C) .
  • the laminating step was performed by first laying the adhesive substrate in such a way that the adhesive layer and the ink imaged layer of the imaged receptor element were contacting each other.
  • the composite was then passed through the hot nip of an IT 6000 hot roll laminator at a speed of 2 feet/minute ( ⁇ 1.02 cm/second), at a temperature of 250°F ( ⁇ 121°C) and at a pressure of 100 psi ( ⁇ 7.0 kg/cm 2 ).
  • the polyethylene terephthlate, temporary carrier layer contiguous to the protective layer was stripped therefrom to form a protected ink image on the substrate.
  • the surface of the protected ink image produced could withstand scribing with a 4H pencil with no removal of the protective layer or image.
  • Example 3 An ink receptor element was prepared as follows: An abrasion resistant coating solution was prepared as disclosed in example 1.
  • An adhesive, ink receptive coating solution was prepared from the following ingredients: Ingredient Parts By Weight Ethanol 30.841
  • (3) - Joncryl ® 61LV acrylic resin solution is, by weight, 35% Joncryl ® 678 acrylic resin, 51% water, 5% isopropanol, 1.5% ethylene glycol, and 7.5% Ammonia (28%); the resin has an acid number of 70 and a Tg of 95°C; and is a product of S.C. Johnson & Son, Inc., Racine, Wisconsin.
  • PVP K-90 is 2-Pyrrolidone methenyl homopolymer which has a viscosity average molecular weight of 700,000 and is a product of GAF Chemicals Corporation, Wayne eMs ⁇ y.
  • - Amorphous silica is Syloid ® 620 and is a product of Davison Chemical Division of W.R. Grace & Co., Baltimore, Maryland.
  • (6) - Zonyl ® FSJ is an anionic fluorosurfactant and is a product of E.I. du Pont de Nemours & Co., Wilmington Delaware.
  • - Rovace ® HP-2931 is a vinyl acetate/ acrylic copolymer aqueous emulsion containing 50% solids, and is a product of Rohm & Haas Company, Philadelphia, Pennsylvania.
  • the above ingredients were added in the order shown and mixed in a Lightnin ® mixer at medium speed until all ingredients were fully incorporated (about 1 hour).
  • the solution was overcoated onto the previously coated protective layer using a #38 meyer rod and dried at 240°F ( ⁇ 115°C) for two minutes to give a dry coating thickness of 9.1 ⁇ m to form the image transparent, adhesive, ink receptive layer of the ink receptor element.
  • the substrates used to demonstrate the process of this invention were; a sheet of 0.0055 inch ( ⁇ 0.14 mm) thick vinyl coated with an ink receptive layer and backed with a 10 pt. paper liner (Flexmark ® CV600 W, manufactured by Flexcon Co., Inc.); an adhesively backed sheet of 0.004 inch ( ⁇ 0.1 mm) thick untreated cast vinyl polymer having a removable release liner; a sheet of Rexcal ® 4000-000 white cast vinyl sheet (a product of Rexham Branded Products, Lancaster, South Carolina); a sheet of TYPAR ® spunbonded polypropylene fabric with an acrylic primed surface (a product of Eastern Banner Supply, Moorsesville, Indiana; a corrugated cardboard paper product; and an unfinished hardwood plank.
  • a sheet of 0.0055 inch ( ⁇ 0.14 mm) thick vinyl coated with an ink receptive layer and backed with a 10 pt. paper liner (Flexmark ® CV600 W, manufactured by Flexcon
  • the laminating step was performed by first laying each substrate in such a way that the substrate surface and the ink imaged layer of each imaged receptor element were contacting each other. Each composite was then passed through the hot nip of an IT 6000 hot roll laminator at a speed of 2 feet/minute ( ⁇ 1.02 cm/second), at a temperature of 250°F ( ⁇ 121°C) and at a pressure of 100 psi ( ⁇ 7.0 kg/cm 2 ). After each laminated element exited from the hot nip, it was held for 30 seconds and then the polyethylene terephthlate, temporary carrier layer contiguous to the protective layer was stripped therefrom to form a protected ink image on each of the three substrates.
  • each protected ink image produced could withstand scribing with a 4H pencil with no removal of the protective layer or image.
  • the protected ink image on the static cling vinyl can be used as a removable decal on a substrate, e.g., a window.
  • the protected ink image on the adhesive backed vinyl can be mounted by the adhesive backing to the surface of a substrate to form a mounted protected image, e.g., a poster, billboard, sign, and the like.
  • the protected ink image on the cast white vinyl sheet can be used as a back lighted display.
  • the protected ink image on the spunbonded polypropylene fabric can be used as a banner.
  • the protected ink image on the corrugated cardboard can be used in product packaging.
  • the protected ink image on the untreated hardwood can be used as a decorative decal on furniture or buildings.
  • Example 4 An ink receptor element was prepared as follows: An abrasion resistant coating solution was prepared and coated on a 0.10 mm (-0.004 inch) thick, untreated, polyethylene terephthlate film as described in Example 3. An ink receptive coating solution was prepared as in example 1 above. The solution was overcoated onto the previously coated protective layer using a #38 meyer rod and dried at 240 ⁇ F ( ⁇ 115°C) for two minutes to give a dry coating thickness of 8.1 ⁇ m to form the image transparent, ink receptive layer of the ink receptor element.
  • An adhesive layer coating solution was prepared from the following ingredients, ingredient par s 3y weight
  • Amorphous silica (ave. particle size 3 ⁇ m) 4.00
  • the coating solution was made by mixing the ingredients in the order shown with a high speed Lightnin* mixer and stirred for 1 hour.
  • the solution was overcoated onto the previously coated protective layer using a meyer rod and dried at 240 ⁇ F ( ⁇ 115 * C) for one minute to form the image transparent, adhesive layer of the ink receptor element.
  • An 8.5 inch x 11 inch ( 21.6 cm x 27.9 cm) sheet was cut from the ink receptor element prepared supra.
  • a color image was printed on the ink receptive layer of the sheet using an Hewlett-Packard Deskjet* 500C color printer using the manufacturer's recommended inks and printing conditions.
  • the laminating step was performed by first laying a sheet of an adhesively backed sheet of 0.004 inch ( ⁇ 0.1 mm) thick untreated cast vinyl polymer having a removable release liner in such a way that the vinyl polymer surface and the ink imaged layer of the imaged receptor element were contacting each other.
  • the composite was then passed through the hot nip of an IT 6000 hot roll laminator at a speed of 2 feet/minute ( ⁇ 1.02 cm/second), at a temperature of 250°F ( ⁇ 121°C) and at a pressure of 100 psi ( ⁇ 7.0 kg/cm 2 ).
  • the polyethylene terephthlate, temporary carrier layer contiguous to the protective layer was stripped therefrom to form a protected ink image on the vinyl polymer substrate.

Landscapes

  • Ink Jet Recording Methods And Recording Media Thereof (AREA)

Abstract

A novel three step process is disclosed for the manufacture of protected, full-color ink jet images for use on large format posters, billboards and the like. An ink receptive element (10), which is used in the process, comprises a temporary carrier layer (12); a protective layer (14), and an ink receptive layer (18). The novel imaging process comprises: A) depositing an ink image layer (17) on the surface of the ink receptive element (10), so that the ink image layer (17) is adhered to the surface of the ink receptive layer (18); B) pressure laminating and adhering a receptor substrate (20) to the ink image layer (17) to form a laminated image element (30); and C) removing the temporary carrier layer (12) from the protective layer (14) of the laminated image element (30) to form a protected imaged substrate (40).

Description

TITLE INK JET IMAGING PROCESS AND RECORDING ELEMENT
BACKGROUND OF THE INVENTION
Field of the Invention
This invention relates to ink jet printing processes for making images, and particularly, color images. More particularly, this invention relates to ink jet printing processes and the elements used therein for the production and protection of large size, full color images.
Description of Related Art
The use of ink jet printing processes in the manufacture of multicolor images is well known in the art. In such processes, ink droplets are emitted from a nozzle and deposited on substrates, such as paper, to form an image. In order to obtain good quality images, rapid absorption of the ink into the substrate is required, but at the same time the ink colorant must be retained at or near the surface of the substrate with lateral ink migration limited to the resolution of the printer. Ink jet printing and its use in making full color images is reviewed in general by Werner E. Haas in "Non- Impact Printing Technologies": Chapter 13, pages 379-384, of IMAGING PROCESSES AND MATERIALS - NEBLETTE'S EIGHTH EDITION, Edited by John Sturge, Vivian Walworth & Allan Shepp, (1989) Van Nostrand Reinhold, New York. To achieve high quality images in ink jet printing, the substrate, e.g., paper, is coated with a formulation to meet the requirements discussed supra. Although paper stock is extensively used as the substrate for ink jet printing, many other materials are used including plastic films and sheets, and the like. When transparencies are to be produced, typically a coated transparent plastic film or sheet is used as the substrate. Since aqueous based inks are the common type of ink used in ink jet printing processes, substrate coating formulations typically are hydrophilic and contain appropriate absorptive materials.
Current ink jet printing processes, inks and substrates are capable of producing high quality four color images in sizes ranging from office copy up to sizes useful for posters, displays and billboards. However, application of ink jet printing has been limited largely to such uses as office copy and the like where environmental and abrasion damage to the finished ink image is unlikely. When used as posters, displays and particularly billboards, the water sensitive ink jet image and underlying substrate must be protected from rain, sunlight, and other environmental contaminants and should likewise be protected from abrasion and graffiti to provide adequate useful life to the image displayed.
An image protective film and its method of use is disclosed in Yoshida, U.S. Patent 5,217,773; the film comprises a base layer, a release layer formed of a resin having no compatibility with the base layer and an adhesive layer formed of a thermoadhesive resin. The film is superposed on an image surface of an object article such that the adhesive layer comes in contact with the image surface and thereafter heated. The base layer is separated from the object article and the adhesive layer and the release layer remain on the object article to form a protective layer.
Although advances have been made in providing protection for color ink jet images on substrates which are flat or planar, there is an industry need for a method for applying protected, distortion-free, ink jet images to objects having non-planar topography. There also continues to be an industry need for a simplified process to provide protected, distortion-free, full-color ink jet images, particularly, for use on large format posters, billboards, metals, wood, glass, rigid plastics and the like.
SUMMARY OF THE INVENTION These needs are met by the ink jet imaging process of this invention which is a process for preparing a protected ink image comprising:
A) imagewise depositing one or more ink images on an ink receptor element, the ink receptor element comprising
1) a temporary carrier layer; 2) an image transparent, protective layer; and
3) an image transparent, ink receptive layer permanently adhered to the protective layer, wherein, the one or more ink images are deposited on the image transparent, ink receptive layer to form an imaged ink receptive layer;
B) permanently adhering to the imaged ink receptive layer to form an imaged laminate, a substrate comprising: a) a support; and b) a first adhesive layer on a first surface of said support, by contacting said first surface of said substrate to said imaged ink receptive layer, and,
C) removing the temporary carrier layer from the image transparent, protective layer of the imaged laminate. In an added embodiment of this invention, the first adhesive layer of the substrate is omitted and the ink receptive layer includes an adhesive which is activated to permanently adhere the imaged ink receptive layer to the substrate. In still an added embodiment of this invention, the substrate further comprises: c) a second adhesive layer on a second surface of said support opposite said first surface; and optionally, d) a removable cover sheet temporarily adhered to the second adhesive layer; and in performing step (B) the substrate is oriented so that the surface of the substrate bearing the second adhesive layer is away from the imaged ink receptive layer and either before or after step (C) , there is performed the additional step: D) removing the removable cover sheet, if present, from the adhesive layer and adhering the adhesive layer of the imaged laminate to a second substrate to form a mounted, imaged laminate.
A further embodiment of this invention is an ink recording element comprising:
1) a temporary carrier layer;
2) an image transparent, protective layer; and
3) an image transparent, ink receptive layer permanently adhered to the protective layer, wherein, the image transparent, ink receptive layer is receptive to aqueous ink jet inks and comprises a hydrophilic resin material and, optionally, an adhesive material.
BRIEF DESCRIPTION OF THE DRAWINGS The invention can be more fully understood from the following description thereof in connection with the accompanying drawings described as follows:
Figure 1 is a cross section view illustrating details of the ink deposition step of the process of this invention and an ink receptive element used therein.
Figure 2 is a cross section view illustrating details of the imaged ink receptive element and the substrate.
Figures 3a and 3b are cross section views illustrating subsequent process steps of this invention using the element of figure 2.
Figure 4 is a cross section view illustrating details of an alternate embodiment of the imaged ink receptive element and the substrate.
Figures 5a and 5b are cross section views illustrating subsequent process steps of this invention using the element of figure 4.
DETAILED DESCRIPTION OF THE INVENTION This invention will now be described by reference to the accompanying drawings. Throughout the following description, similar reference characters refer to similar elements in all figures of the drawings.
The first process step (A) comprises imagewise depositing one or more ink images on an ink receptor element. Referring to Figure 1, an ink jet device (11) traversing in a direction (19) across an ink receptor element, imagewise deposits ink droplets (17) on an image transparent, ink receptive layer (16) to form an imaged ink receptive layer (18). The imaged ink receptor element (10) which is formed comprises; a temporary carrier layer (12), an image transparent, protective layer (14), and an image transparent imaged ink receptive layer (18) .
The ink jet device (11) which is used to generate an image on the imaged ink receptive layer (18) may be any of the conventional ink jet printers used to print a single color or a full color image as disclosed by Werner E. Haas in "Non- Impact Printing Technologies": Chapter 13, pages 379-384, supra. Additional ink jet devices include Hewlett Packard Desk Jet 500 and 500C printers; IBM Lexmark® ink jet printers; Cannon Bubblejet® printers; ENCAD Computer Corporation Novajet® printers; and the like.
In the practice of this invention, either a one color ink image, e.g. , black, is deposited; or several colors are deposited either in sequence or simultaneously, to form an imaged ink receptive layer (18), e.g., a four color subtractive color image consisting of yellow, magenta, cyan and black images in register. Unless the imaged ink receptive layer (18) is to be used in the manufacture of a transparency, the ink image typically is printed on the ink receptive layer (16) as a reverse or mirror image so that the completed protected ink image will possess correct orientation when applied to an opaque substrate.
The inks used in the ink imaging process of this invention are well known for this purpose. The ink compositions used, typically are liquid compositions comprising a solvent or carrier liquid, dyes or pigments, humectant, organic solvents, detergents, thickeners, preservatives, and the like. The solvent or carrier liquid typically is water, although ink in which organic materials such as polyhydric alcohols as the predominant solvent or carrier also are used. The dyes used in such compositions are typically water-soluble direct or acid type dyes. Such liquid ink compositions have been extensively described in the prior art, e.g. , such as disclosed by P. Gender in "Materials Aspects For High Quality Color Thermal Ink Jet Printing" IS&T's 46th Annual Conference (1993), pages 175-177.
Referring now to Figure 2, details of the imaged receptor element (10) and substrate (20) are illustrated. In preparation for the second step of the process of this invention, the imaged receptor element (10) is oriented to a substrate (20), comprising a support (22) and a first adhesive layer (24) applied to a first surface of the support, so that the surface of the adhesive layer (24) faces the surface of the imaged ink receptive layer (18) The temporary carrier layer (12) of the ink receptor element (10) functions as a temporary support to the superposed layers during the process steps of this invention and may be any web or sheet material possessing suitable flexibility, dimensional stability and adherence properties to the protective layer (14). Typically, the web or sheet material is a flexible polymeric film, e.g. , such as polyethylene terephthalate film and the like, or a foraminous material, e.g., such as a paper sheet and the like. The web or sheet may also be surface treated or coated with a material to enhance desired release characteristics, e.g., such as treatment with a silicone release agent and the like.
The protective layer (14) of the ink receptor element (10) is a polymeric film material which is resistant to scratching, abrasions and the like, and to environmental components and contaminants. The protective layer (14) is permanently adhered to the image transparent, ink receptive layer (16) while being only temporarily adhered to the temporary carrier layer (12). The protective layer (14) is visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region. Polymeric materials which are useful in making this layer include polyvinyl chloride; polyvinylidene chloride; fluorinated polymers and copolymers; polyvinyl butyral; cellulose acetate propionate; cellulose acetate butyrate; polyesters; acrylics; fluorinated polymers; polyurethanes; styrene copolymers, e.g., such as styrene acrylonitrile; and combinations thereof. This layer may contain components which strongly absorb ultraviolet radiation thereby reducing damage to underlying images by ambient ultraviolet light, e.g., such as 2-hydroxy-benzophenones; oxalanilides; aryl esters and the like; hindered amine light stabilizers, such as bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate and the like; and combinations thereof. This layer may also contain components which provide protection from biological attack, such as, fungicides and bactericides, and the like.
The protective layer (14) may be provided with a matt surface. This matt surface can be obtained by including in the layer particles sufficiently large to give surface irregularities to the layer, or may be imparted or embossed by the surface characteristics of the temporary carrier layer (12). Particles of average diameter in the range of about 1 μm to about 15 μm are suitable. The protective layer also may be provided with a graffiti-proof surface, typically, a perfluorinated polymer surface. The protective layer (14) typically has a thickness in the range of about 0.5 μm to about 20 μm and preferably in the range of about 3 μm to about 10 μm. Such layers typically will withstand scribing with the point of a 4H pencil without breakthrough. The image transparent, ink receptive layer (16) of the ink receptor element (10), is permanently adhered to the protective layer (14), and is a hydrophilic, aqueous ink sorptive, coating material. The ink receptive layer (16) is visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region. The visible spectral region of the ink receptive layer (16) typically is matched to that of the protective layer (14). The image transparent, ink receptive layer (16) may be prepared from a wide variety of hydrophilic, aqueous ink sorptive, coating materials. In current industry practice, the ink receptive layer (16) typically is formulated to provide suitable ink receptivity tuned for a particular ink jet device (11) and related ink (17) used therein. In general, suitable formulations for the ink receptive layer (16) are disclosed in Desjarlais, U.S. Patent 4,775,594; Light, U.S. Patent 5,126,195; and Kruse, U.S. Patent 5,198,306. The ink receptive layer (16) typically is comprised of at least one hydrophilic polymer or resin which also may be water soluble. Suitable hydrophilic polymers or resins include polyvinyl alcohols, including substituted polyvinyl alcohols; polyvinyl pyrrolidones, including substituted polyvinyl pyrrolidones; vinyl pyrrolidone/vinyl acetate copolymer; vinyl acetate/acrylic copolymers; acrylic acid polymers and copolymers; acryla ide polymers and copolymers; cellulosic polymers and copolymers; styrene copolymers of allyl alcohol, acrylic acid, malaeic acid, esters or anhydride, and the like; alkylene oxide polymers and copolymers; gelatins and modified gelatins; polysaccharides; and the like. Preferred hydrophilic polymers include polyvinyl pyrrolidone; substituted polyvinyl pyrrolidone; polyvinyl alcohol; substituted polyvinyl alcohol; vinyl pyrrolidone/vinyl acetate copolymer; vinyl acetate/acrylic copolymer; polyacrylic acid; polyacrylamides; hydroxyethylcellulose; carboxyethylcellulose; gelatin; and polysaccharides.
The ink receptive layer (16) may also contain other water insoluble or hydrophobic polymers or resins to impart a suitable degree of hydrophilicity and/or other desirable physical and chemical characteristics. Suitable polymers or resins of this class include polymers and copolymers of styrene, acrylics, urethanes, and the like. Preferred polymers and resins of this type include a styrenated acrylic copolymer; styrene/allyl alcohol copolymer; nitrocellulose; carboxylated resin; polyester resin; polyurethane resin; polyketone resin; polyvinyl butyral resin; or mixtures thereof. In addition to the polymeric or resin components, the ink receptive layer (16) typically contains other added components such as a dye mordant, a surfactant, particulate materials, a colorant, an ultraviolet absorbing material, an organic acid, an optical brightener, and the like. Dye mordants which may be used to fix the printed ink to the ink receptive layer (16) may be any conventional dye mordant, e.g. such as polymeric quaternary ammonium salts, polyvinyl pyrrolidone, and the like. Surfactants which are used as coating aids for the ink receptive layer (16) may be any nonionic, anionic, or cationic surfactant. Particularly useful, are fluorosurfactants, alkylphenoxypolyglycidols, and the like.
The ink receptive layer may also contain particulate material. Such materials are believed to aid in enhancing the smoothness characteristics of the ink receptive surface, particularly after it has been printed upon without adversely affecting the transparent characteristics of the element. Suitable particulate material includes inorganic particles such as silicas, chalk, calcium carbonate, magnesium carbonate, kaolin, calcined clay, pyrophylite, bentonite, zeolite, talc, synthetic aluminum and calcium silicates, diatomatious earth, anhydrous silicic acid powder, aluminum hydroxide, barite, barium sulfate, gypsum, calcium sulfate, and the like; and organic particles such as polymeric beads including beads of polymethylmethacrylate, copoly(methylmethacrylate/divinylbenzene) , polystyrene, copoly(vinyltoluene/t-butylstyrene/methacrylic acid) , polyethylene, and the like. The composition and particle size of the particles are selected so as not to impair the transparent nature of the ink receptive layer (16).
The ink receptive layer (16) may also contain a colorant, e.g., a dye or pigment, provided the layer is visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region. This layer may contain components which strongly absorb ultraviolet radiation thereby reducing damage to underlying images by ambient ultraviolet light, e.g., such as 2-hydroxybenzophenones; oxalanilides; aryl esters and the like; hindered amine light stabilizers, such as bis(2,2,6,6- tetramethyl-4-piperidinyl) sebacate and the like; and combinations thereof. Organic acids which are used to adjust the pH and hydrophilicity in the ink receptive layer (16) typically are non-volatile organic acids such as a alkoxy acetic acid, a glycolic acid, a dibasic carboxylic acid and half esters thereof, a tribasic carboxylic acid and partial esters thereof, aromatic sulfonic acids, and mixtures thereof. Preferred organic acids include glycolic acid, methoxy acetic acid, citric acid, malonic acid, tartaric acid, malic acid, aleic acid, fumaric acid, itaconic acid, succinic acid, oxalic acid, 5-sulfo-salicylic acid, p-toluenesulphonic acid, and mixtures thereof. Optical brighteners which may be used to enhance the visual appearance of the imaged layer may be any conventional, compatible optical brightener, e.g., such as optical brighteners marketed by Ciba-Geigy under the trademark of Tinopal® .
The first adhesive layer (24) of the substrate (20), functions to permanently adhere the imaged ink receptive layer (18) and the protective layer (14) of the imaged receptor element (10), to the substrate during the process of this invention. The adhesive layer (24) may be chosen from a variety of conventional adhesive materials, e.g., such as thermally activated, pressure sensitive, photo-activated, or contact adhesives and the like. Typically, the adhesive material will be a thermally activated adhesive material comprised of thermoplastic polyurethanes; polycaprolactone; acrylic copolymers; and combinations thereof. Representative thermally activated adhesive materials include Morthane® CA- 116 urethane resin (a product of Morton International); Tone® Polymer P767E biodegradable plastic resin (a product of Union Carbide); Elvax® 240 Ethylene vinyl acetate (a product of Dupont Chemicals); and the like.
The support (22) of the substrate (20) typically functions as the final support for the protected imaged ink receptive layer (18) formed during the process steps of this invention. The support (22) may be any surface upon which an ink jet image is desired. Typically, it is a web or sheet material possessing dimensional stability and adherence properties through the adhesive layer (24) to the imaged ink receptive layer (18) of the imaged ink receptor element (10). The web or sheet material may be a flexible polymeric film, e.g., such as polyethylene terephthalate film and the like; a foraminous material, e.g., such as a paper sheet, textile fabrics, and the like; metal films or webs, e.g., such as aluminum, steel, tin-plate, and the like; or any composites or laminates thereof. The support (22) may be a rigid or semi¬ rigid sheeting or plate, e.g., such as sheeting or plates of metal, glass, ceramic, plastic, cardboard, or any composites or laminates thereof. The support (22) may vary in size from that of a photographic print, e.g., having an area of about 30 cm2 or less, to that of vehicle sign or billboards, e.g., having an area of about 70 m2 or greater. Since the thin protective (14) and ink receptive (16) layers are highly compliant, the support (22) also may vary in shape and surface topography, e.g., spherical, embossed, etc. When a transparency is to be produced by the process of this invention, the support (22) and first adhesive layer (24) are visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region. This layer may also contain components which strongly absorb ultraviolet radiation thereby reducing damage to underlying images by ambient ultraviolet light, e.g., such as 2-hydroxybenzophenones; oxalanilides; aryl esters and the like; hindered amine light stabilizers, such as bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate and the like; and combinations thereof. The web or sheet may also be surface treated or coated with a material to enhance desired surface characteristics, e.g. sub-coatings, electric discharge treatment, and the like. By careful selection of the adhesive system, the imaged ink receptor element (10) can be applied to most solids or foraminous materials, e.g., adhesive backed vinyl, static cling vinyl, and polyethylene terephthlate films; steel, glass, ceramic, and wood sheets and objects. The substrate (20) may further have a second adhesive layer adhered to a second surface of the support (22) opposite the first surface, e.g., the reverse side; and optionally a removable cover sheet may be temporarily adhered to the second adhesive layer. The adhesive material of the second adhesive layer may be any contact, thermal or pressure sensitive adhesive, such as described supra, and may be an integral part of the substrate (20) or it may be applied just prior to a mounting step. Typically, a removable cover sheet is temporarily adhered to the adhesive surface(s) of the substrate (20) to protect against damage during storage or preliminary handling. The removable cover sheet may be any conventional release cover sheet.
The ink imaging process of this invention comprises three process steps of which the initial process step (A) of producing an imaged receptor element (10) has been described, supra, by reference to Figure 1. The remaining steps of the process will now be described by reference to Figures 3a and 3b.
The second process step (B) comprises applying to the imaged ink receptive layer (18) of the ink receptor element (10), the surface of the first adhesive layer (24) of the substrate (20) .
Referring to Figure 3a, the first adhesive layer (24) is contacted and permanently adhered to the imaged ink receptive layer (18) using an applied pressure (31) to the surfaces of the temporary carrier layer (12) and the support (22) to form an imaged laminate (30). When only a pressure sensitive adhesive is used, the applied pressure (31) must be sufficient to activate the adhesive to form a permanent bond between the layers. The adhesive substrate (20) is typically applied to the imaged ink receptive layer (18) under an applied pressure (31) of atmospheric pressure or greater. The applied pressure (31) may be about 0.07 kg/cm2 (1 p.s.i.) to about 7 kg/cm2 (100 p.s.i.) or greater. The term "applied pressure" is intended to mean the absolute pressure which is applied to a unit area of the surface as conventionally derived from the geometry of the pressure means, e.g., the geometry of the laminating nip, in combination with a measurement means, e.g., a calibrated gauge pressure. Suitable means that may be used to apply pressure include platen presses; counterpoised, double roll, laminating devices; vacuum laminating devices; scanning, single roll, laminating devices; hand-held, rollers and squeegees; and the like. Typically roll laminating devices are preferred since they readily minimize air entrapment between the adhesive layer (24) and the imaged ink receptive layer (18) during the application process step. Vacuum may be applied with such devices to further eliminate air entrapment. Typically, the adhesive layer (24) is a thermally activated adhesive. In this instance, heat is typically applied to the adhesive layer (24) prior to and/or concurrently with the application of the applied pressure (31). While the temperature used to activate the adhesive depends on the nature of the material, the adhesive substrate (20) is applied to the imaged ink receptive layer (18) at a temperature of about 80°C or greater and preferably about
100°C or greater. Typical application temperatures range from about 100°C to about 200°C. Typically, temperature is measured on the surface of the heated roll or platen by means of temperature sensitive tape. Thus the adhesive substrate (20) may be heated prior to its application by radiant or contact heaters and then applied while hot to the imaged ink receptive layer (18).
Alternatively the pressure means itself may also function as a heater, e.g. , such as a hot roll laminator, or both prior and concurrent heating may be used in combination. The adhesive layer (24) may also be a photo-activated adhesive. In this instance, the adhesive layer (24) typically is irradiated with actinic radiation either concurrently with or subsequent to the application of the applied pressure (31). In this instance, the support (22) and/or any intervening layer should be sufficiently transparent to the actinic radiation which activates the photo adhesive. When the adhesive layer (24) is thermally or photo activated, the applied pressure (31) may be just sufficient to bring the surface of the adhesive layer (24) into intimate contact with the surface of the imaged ink receptive layer (18).
The third process step (C) comprises removing the temporary carrier layer (12) from the surface of the protective layer (14) of the imaged laminate (30). Referring to Figure 3b, the temporary carrier layer (12) is peeled, using a peel force (41), from the surface of the protective layer (14) to form the completed protected ink image element (40). Typically, the temporary carrier layer (12) is peeled with a peel force (41) directed at an angle of 90° or more from the surface of the protective layer (14). The peel rate and the peel force (41) are not critical and preferred values will depend on the nature of the protective and carrier materials. The temperature at which the temporary carrier layer (12) is peeled form the protective layer (14) will depend on the nature of the substrate, adhesive, protective and carrier materials used in the imaged laminate (30). The temporary carrier layer (12) may be peeled at room temperature or, alternatively, the imaged laminate (30) may be heated to facilitate removal of the temporary carrier layer (12). When a thermally activated adhesive material is used to form the imaged laminate (30), it surprisingly has been found that the temporary carrier layer (12) can be removed immediately after formation of the imaged laminate (30) (i.e., while still in a heated state from the application process step (B)) without delamination of the thermal first adhesive layer (24) or any of the other component layers. In this context, the term "immediately" is intended to mean a time span of about 1 minute or less and preferably between about 1 second and about 20 seconds. Alternatively, when a thermally activated adhesive material is used to form the imaged laminate (30), the laminate may be cooled and stored before removal of the temporary carrier layer (12). In this instance, the temporary carrier layer (12) can be removed at room temperature from the imaged laminate (30) without delamination of the first adhesive layer (24) or any of the other component layers.
Alternatively, the imaged laminate (30) may be reheated prior to removal of the temporary carrier layer (12). In this instance, the laminate typically is reheated to a temperature which is within about ± 5°C of the temperature used to form the element in process step (B) . To further protect the imaged laminate (30) from damage before its use, the temporary carrier layer (12) may be kept adhered to the imaged laminate (30) during its intermediate storage and handling, and then removed just prior to use. In the added embodiment of this invention, the adhesive substrate (20) further comprises a second adhesive layer adhered to a second surface of the support (22) opposite the first surface; and optionally, there is a removable cover sheet temporarily adhered to the second adhesive layer. In this embodiment, the process further comprises; either before or after step (C) , the added step (D) of removing the removable cover sheet, if present, from the second adhesive layer and adhering the second adhesive layer of the protected ink image element (40) to a second substrate to form a mounted, imaged laminate. This embodiment is particularly useful for preparing component protected image "tiles" and then mounting each tile to form a composite display image such as on a billboard or the like. In this instance, depending on the end use, the mounting adhesive may be either permanent or temporary.
Referring to Figure 4, details of an alternate imaged receptor element (110) and substrate (122) are illustrated.
Ink receptor element (110) includes a temporary carrier layer 12 and a protective layer 14 as herein above described. An image transparent, adhesive, ink receptive layer (116) is permanently adhered to the image transparent, protective layer (14), and provides a dual function of ink receptivity as well as an adhesive to the ink receptor element (110). The material of the image transparent, adhesive, ink receptive layer (116) is a hydrophilic, aqueous ink sorptive, coating material as well as an adhesive which, when activated, functions to adhere the protected image to the substrate (122). The adhesive, ink receptive layer (116) may be a blend of the necessary materials in a single layer, or it may be a composite of two or more individual layers wherein one layer would contain the major character of the ink receptive material and the other would contain the major character of an adhesive material and in part a shared character of the ink receptive material. The adhesive, ink receptive layer (116) is visually transparent in at least one region within the visible spectral region and typically is transparent throughout the visible spectral region. The visible spectral region of the adhesive, ink receptive layer (116) typically is matched to that of the protective layer (14) as stated earlier. The image transparent, adhesive, ink receptive layer (116) may be prepared from a wide variety of hydrophilic, aqueous ink sorptive, coating materials again as herein above described.
After imaging, the adhesive material of the image transparent, adhesive, ink receptive layer (116), becomes imaged layer (118) and functions to permanently adhere itself and protective layer (14) of the imaged receptor element (110), to substrate (122) during the process of this invention. The adhesive material may be chosen from a variety of conventional adhesive materials, e.g., such as thermally activated, pressure sensitive, photo activated, or contact adhesives and the like, provided it is compatible with the components of the ink receptive material and that it contributes, at least in part, to ink receptivity. The term "compatible" is intended to mean that the adhesive material may be dispersed within the image transparent, adhesive, ink receptive layer (16) without substantially altering the image transparency or ink receptivity of the layer. Typically, the adhesive material will be a thermally activated, hydrophilic, adhesive material comprised of thermoplastic polyurethanes; polycaprolactone; acrylic copolymers; and combinations thereof. Representative thermally activated adhesive materials include Rovace® HP-2931 vinyl acetate/acrylic copolymer (a product of Rohm & Haas Company); Morthane® CA- 116 urethane resin (a product of Morton International); Tone® Polymer P767E biodegradable plastic resin (a product of Union Carbide); Elvax® 240 Ethylene vinyl acetate (a product of Dupont Chemicals); and the like. In the instance when the adhesive material is blended into the ink receptive material to form a single layer, preferred adhesive materials are vinyl acetate/acrylic copolymers. In the instance when the adhesive material is coated as a separate layer onto the ink receptive layer, preferred adhesive materials are polycaprolactones. When the adhesive material is coated as a separate layer, the layer typically has a thickness in the range of about 0.5 μm to about 10 μm.
When the element of figure 4 is used, the ink imaging process of this invention comprises three process steps of which the initial process step (A) of producing an imaged receptor element (110) is the same as was described above by reference to Figure 1. The remaining steps of the process may be described by reference to Figures 5a and 5b.
The second process step (B) comprises applying to the imaged layer (118) of the imaged receptor element (110), the surface of the substrate (122). Referring to Figure 5a, the substrate (122) is contacted and adhered to the imaged ink receptive layer (118) using an applied pressure (131) to the surfaces of the temporary carrier layer (12) and the substrate (122) to activate the adhesive and form an imaged laminate (130). The application and adhering steps used are similar to the steps disclosed above in describing the process wherein the element used had no adhesive in the ink receptive layer. When only a pressure sensitive adhesive is used, the applied pressure (131) must be sufficient to activate the adhesive to form a permanent bond between the layers.
The third process step (C) again comprises removing the temporary carrier layer (12) from the surface of the protective layer (14) of the imaged laminate (130). Referring to Figure 5b, the temporary carrier layer (12) is peeled, using a peel force (41), from the surface of the protective layer (14) to form the completed protected element (140).
As discussed above the, the substrate (122) may again further comprise an second adhesive layer adhered to a surface thereof and, optionally, a removable cover sheet temporarily adhered to the second adhesive layer. Again as described above, in this instance the process further comprises; either before or after step (C) , the added step (D) of removing the removable cover sheet, if present, from the adhesive layer and adhering the adhesive layer of the protected ink image element (140) to a second substrate to form a mounted, imaged laminate.
Another embodiment of this invention, comprises an added step wherein after step (C) , the image transparent, protective layer along with the image transparent, adhesive, imaged ink receptive layer are removed intact from the substrate. In addition, after the image transparent, protective layer along with the image transparent, adhesive, imaged ink receptive layer are removed from the substrate, they may be reapplied to the same substrate or to a second substrate. These added steps allow for the complete removal of the adhered layers after a period of use, e.g., removal of a promotional display from a window. Alternatively, the adhered layers may be partially or totally removed, realigned, and then reapplied to the substrate or another substrate, e.g., for display in another window.
The ink imaging process of this invention will now be illustrated by the following examples but is not intended to be limited thereby.
Example 1 An ink receptor element was prepared as follows: An abrasion resistant coating solution was prepared from the following ingredients.
Ingredient Parts By Weight
NeoRez® R-96791) polyurethane 90.0 Tinuvin® 1130< ) UV absorber 5.0 Ethanol 5 . 0
(1) - NeoRez® R-9679 is an aliphatic aqueous colloidal dispersion of a urethane polymer containing 37% by weight solids (specific gravity of solids is 1.16 and acid number of resin solids is 17.0), and is a product of Zeneca Resins, Inc., Wilmington, Massachusetts.
(2) - Tinuvin® 1130 UV absorber, a product of Ciba-Geigy, is the reaction product of polyethylene glycol 300 and the methyl ester of beta-(3-(2h-benzotriazole-2-yl)-4- hydroxy-5-tert-butylphenyl)propionic acid.
The Tinuvin® 1130 was dissolved in the ethanol to form a 50% by weight solution. The Tinuvin® solution was stirred into the NeoRez® R-9679 aqueous dispersion in a Lightnin® mixer at slow speed and mixed for ten minutes. The resulting dispersion was then coated on a 0.10 mm (-0.004 inch) thick, untreated, polyethylene terephthlate film (the temporary carrier layer) using a #16 meyer rod and dried at 240°F (115°C) for two minutes to form the image transparent, protective layer having a dry coating thickness of 3.6 μm. The Tinuvin® 1130 UV absorber in the protective layer blocks about 90% of the incident UV radiation having a wavelength between 310 and 380 nm. An ink receptive coating solution was prepared from the following ingredients:
Ingredient Parts By Weight
Ethanol 46.242
Deionized water 31.136
Joncryl® 61LV<3> acrylic resin 11.610 PVP K-90, Polyvinylpyrrolidone^ 8.770
Amorphous silica (ave. particle size 15 μm)<5) 0.067 Zonyl® FSJ(6) fluorosurfactant 0.023
(3) - Joncryl® 61LV acrylic resin solution is, by weight, 35% Joncryl® 678 acrylic resin, 51% water, 5% isopropanol, 1.5% ethylene glycol, and 7.5% Ammonia (28%); the resin has an acid number of 70 and a Tg of 95°C; and is a product of S.C. Johnson & Son, Inc., Racine, Wisconsin. (4) - PVP K-90 is polyvinylpyrrolidone which has a viscosity average molecular weight of 700,000 and is a product of GAF Chemicals Corporation, Wayne, New Jersey. (5) - Amorphous silica is Syloid® 620 and is a product of Davison Chemical Division of W.R. Grace & Co., Baltimore, Maryland. (6) - Zonyl® FSJ is an anionic fluorosurfactant and is a product of E.I. du Pont de Nemours & Co., Wilmington Delaware.
The above ingredients were added in the order shown and mixed in a Lightnin® mixer at medium speed until all ingredients were fully incorporated (about 1 hour) . The solution was overcoated onto the previously coated protective layer using a #38 meyer rod and dried at 240°F (~ 115°C) for two minutes to give a dry coating thickness of 8.1 μm to form the image transparent, ink receptive layer of the ink receptor element. An adhesive substrate was made as follows: An adhesive layer coating solution was prepared from the following ingredients.
Ingredient Parts By Weight Methyl ethyl ketone 79.96
Toluene 10.00
Morthane® CA-116 urethane resin< 10.00
Amorphous silica (ave. particle size 3 μm) 0.04
(7) - Morthane® CA-116 urethane resin is a product of
Morton-Thiokol and is a hydroxyl terminated polyurethane elastomer.
The coating solution was made by mixing the methyl ethyl ketone, toluene and urethane resin for 30 minutes with a high speed Lightnin® mixer. Amorphous silica was then added and mixed for 5 minutes. The solution was coated onto a sheet of 0.0055 inch (~ 0.14 mm) thick static cling vinyl coated with an ink receptive layer and backed with a 10 pt. paper liner (Flexmark® CV600 W, manufactured by Flexcon Co., Inc.) using a #12 meyer rod and dried at 240°F (115°C) for two minutes to give a dry coating thickness of 2.0 μm to form the adhesive layer of the adhesive substrate. Four additional adhesive substrates were prepared in the same manner except the substrates were an adhesively backed sheet of 0.004 inch (~ 0.1 mm) thick untreated cast vinyl polymer having a removable release liner; a sheet of Rexcal® 4000-000 white cast vinyl sheet (a product of Rexham Branded Products, Lancaster, South Carolina); a sheet of TYPAR® spunbonded polypropylene fabric with an acrylic primed surface (a product of Eastern Banner Supply, Moorsesville, Indiana; and a corrugated cardboard paper product. Five 8.5 inch x 11 inch ( 21.6 cm x 27.9 cm) sheets were cut from the ink receptor element prepared supra. A four color image was printed on the ink receptive layer of each sheet using an IBM Lexmark® ink jet printer using the manufacturer's recommended inks and printing conditions. RH was maintained between 50% and 70%, and temperature was maintained between 65°F (~ 18.3°C) and 75°F (~ 23.8°C).
The laminating step was performed by first laying each adhesive substrate in such a way that the adhesive layer of the adhesive substrate and the ink imaged layer of each imaged receptor element were contacting each other. Each composite was then passed through the hot nip of an IT 6000 hot roll laminator at a speed of 2 feet/minute (~ 1.02 cm/second), at a temperature of 270°F (~ 132°C) and at a pressure of 100 psi (~ 7.0 kg/cm2). As each laminated element exited from the hot nip, the polyethylene terephthlate, temporary carrier layer contiguous to the protective layer was stripped therefrom to form a protected ink image on each of the five substrates. The surface of each protected ink image produced could withstand scribing with a 4H pencil with no removal of the protective layer or image.
The protected ink image on the static cling vinyl can be used as a removable decal on a substrate, e.g., a window. The protected ink image on the adhesive backed vinyl can be mounted by the adhesive backing to the surface of a substrate to form a mounted protected image, e.g., a poster, billboard, sign, and the like. The protected ink image on the cast white vinyl sheet can be used as a back lighted display. The protected ink image on the spunbonded polypropylene fabric can be used as a banner. The protected ink image on the corrugated cardboard can be used in product packaging.
Example 2 An ink receptor element was prepared as described in Example 1 except that the ink receptive coating solution was prepared from the following ingredients: Ingredient Parts By Weight
Polyvinyl alcohol<8) (10% by wt. water solution) 89.97 Polyvinylpyrrolidone< )(10% by wt. water solution) 9.97 Amorphous silica (ave. particle size 1.55 μm)<9 0.03 Amorphous silica (median agglomerate size 1.4 μm)<10) 0.03
(8) - Polyvinyl alcohol is GOHSENAL® T-330H a special grade of Polyvinyl alcohol wherein a 4% water solution at 20°C has a viscosity of 27-32 cps determined by the Hoeppler falling ball method; a hydrolysis of 99-100 mol % (dry basis); and a pH of 6-8.
(9) - Amorphous silica is IMSIL® A-10 and is a product of Illinois Minerals Co., Cairo, Illinois.
(10) - Amorphous silica is Hi-Sil® T-600 and is a product of PPG Industries.
The above ingredients were added in the order shown and mixed in a Lightnin® mixer at medium speed until all ingredients were fully incorporated (about 30 minutes). The solution was overcoated onto the previously coated protective layer using a # 38 meyer rod to give a dry coating thickness of 10 μm to form the image transparent, ink receptive layer of the ink receptor element.
An adhesive substrate was made as described in Example 1 except that the substrate was a sheet of cast coated 0.004 inch (~ 0.1 mm) thick adhesive backed vinyl sheet (Rexcal® 4000-000).
A four color image was printed on the ink receptive layer of the ink receptor element using an IBM Lexmark® ink jet printer using the manufacturer's recommended inks and printing conditions. RH was maintained between 50% and 70%, and temperature was maintained between 65°F (~ 18.3°C) and 75°F (~ 23.8°C) . The laminating step was performed by first laying the adhesive substrate in such a way that the adhesive layer and the ink imaged layer of the imaged receptor element were contacting each other. The composite was then passed through the hot nip of an IT 6000 hot roll laminator at a speed of 2 feet/minute (~ 1.02 cm/second), at a temperature of 250°F (~ 121°C) and at a pressure of 100 psi (~ 7.0 kg/cm2). As the laminated element exited from the hot nip, the polyethylene terephthlate, temporary carrier layer contiguous to the protective layer was stripped therefrom to form a protected ink image on the substrate. The surface of the protected ink image produced could withstand scribing with a 4H pencil with no removal of the protective layer or image.
Example 3 An ink receptor element was prepared as follows: An abrasion resistant coating solution was prepared as disclosed in example 1.
An adhesive, ink receptive coating solution was prepared from the following ingredients: Ingredient Parts By Weight Ethanol 30.841
Deionized water 20.746
Joncryl® 61LV(3) acrylic resin 7.736
PVP K-90 <4) 5.844
Glycerine 1.434 Amorphous silica (ave. particle size 15 μm)(5) 0.044 Zonyl® FSJ(6' fluorosurfactant 0.015
Rovace® HP-2931<7 vinyl acetate/acrylic copolymer 33.340
(3) - Joncryl® 61LV acrylic resin solution is, by weight, 35% Joncryl® 678 acrylic resin, 51% water, 5% isopropanol, 1.5% ethylene glycol, and 7.5% Ammonia (28%); the resin has an acid number of 70 and a Tg of 95°C; and is a product of S.C. Johnson & Son, Inc., Racine, Wisconsin.
(4) PVP K-90 is 2-Pyrrolidone methenyl homopolymer which has a viscosity average molecular weight of 700,000 and is a product of GAF Chemicals Corporation, Wayne eMsβy.
(5) - Amorphous silica is Syloid® 620 and is a product of Davison Chemical Division of W.R. Grace & Co., Baltimore, Maryland. (6) - Zonyl® FSJ is an anionic fluorosurfactant and is a product of E.I. du Pont de Nemours & Co., Wilmington Delaware.
(7) - Rovace® HP-2931 is a vinyl acetate/ acrylic copolymer aqueous emulsion containing 50% solids, and is a product of Rohm & Haas Company, Philadelphia, Pennsylvania.
The above ingredients were added in the order shown and mixed in a Lightnin® mixer at medium speed until all ingredients were fully incorporated (about 1 hour). The solution was overcoated onto the previously coated protective layer using a #38 meyer rod and dried at 240°F (~ 115°C) for two minutes to give a dry coating thickness of 9.1 μm to form the image transparent, adhesive, ink receptive layer of the ink receptor element.
The substrates used to demonstrate the process of this invention were; a sheet of 0.0055 inch (~ 0.14 mm) thick vinyl coated with an ink receptive layer and backed with a 10 pt. paper liner (Flexmark® CV600 W, manufactured by Flexcon Co., Inc.); an adhesively backed sheet of 0.004 inch (~ 0.1 mm) thick untreated cast vinyl polymer having a removable release liner; a sheet of Rexcal® 4000-000 white cast vinyl sheet (a product of Rexham Branded Products, Lancaster, South Carolina); a sheet of TYPAR® spunbonded polypropylene fabric with an acrylic primed surface (a product of Eastern Banner Supply, Moorsesville, Indiana; a corrugated cardboard paper product; and an unfinished hardwood plank.
For each substrate, an 8.5 inch x 11 inch ( 21.6 cm x 27.9 cm) sheet was cut from the ink receptor element prepared supra. A four color image was printed on the ink receptive layer of each sheet using an IBM Lexmark® ink jet printer using the manufacturer's recommended inks and printing conditions. RH was maintained between 50% and 70%, and temperature was maintained between 65°F (~ 18.3°C) and 75°F (~ 23.8°C)
The laminating step was performed by first laying each substrate in such a way that the substrate surface and the ink imaged layer of each imaged receptor element were contacting each other. Each composite was then passed through the hot nip of an IT 6000 hot roll laminator at a speed of 2 feet/minute (~ 1.02 cm/second), at a temperature of 250°F (~ 121°C) and at a pressure of 100 psi (~ 7.0 kg/cm2). After each laminated element exited from the hot nip, it was held for 30 seconds and then the polyethylene terephthlate, temporary carrier layer contiguous to the protective layer was stripped therefrom to form a protected ink image on each of the three substrates. The surface of each protected ink image produced could withstand scribing with a 4H pencil with no removal of the protective layer or image. The protected ink image on the static cling vinyl can be used as a removable decal on a substrate, e.g., a window. The protected ink image on the adhesive backed vinyl can be mounted by the adhesive backing to the surface of a substrate to form a mounted protected image, e.g., a poster, billboard, sign, and the like. The protected ink image on the cast white vinyl sheet can be used as a back lighted display. The protected ink image on the spunbonded polypropylene fabric can be used as a banner. The protected ink image on the corrugated cardboard can be used in product packaging. The protected ink image on the untreated hardwood can be used as a decorative decal on furniture or buildings.
Example 4 An ink receptor element was prepared as follows: An abrasion resistant coating solution was prepared and coated on a 0.10 mm (-0.004 inch) thick, untreated, polyethylene terephthlate film as described in Example 3. An ink receptive coating solution was prepared as in example 1 above. The solution was overcoated onto the previously coated protective layer using a #38 meyer rod and dried at 240βF (~ 115°C) for two minutes to give a dry coating thickness of 8.1 μm to form the image transparent, ink receptive layer of the ink receptor element.
An adhesive layer coating solution was prepared from the following ingredients, ingredient par s 3y weight
Toluene 81.0
Propylene glycol monomethyl ether 5.0
Tone® P767-E Polycaprolactone(β> 10.00
Amorphous silica (ave. particle size 3 μm) 4.00
(8) - Tone* P767-E plastic resin is polycaprolactone and is a product of Union Carbide.
The coating solution was made by mixing the ingredients in the order shown with a high speed Lightnin* mixer and stirred for 1 hour. The solution was overcoated onto the previously coated protective layer using a meyer rod and dried at 240βF (~ 115*C) for one minute to form the image transparent, adhesive layer of the ink receptor element. An 8.5 inch x 11 inch ( 21.6 cm x 27.9 cm) sheet was cut from the ink receptor element prepared supra. A color image was printed on the ink receptive layer of the sheet using an Hewlett-Packard Deskjet* 500C color printer using the manufacturer's recommended inks and printing conditions. The laminating step was performed by first laying a sheet of an adhesively backed sheet of 0.004 inch (~ 0.1 mm) thick untreated cast vinyl polymer having a removable release liner in such a way that the vinyl polymer surface and the ink imaged layer of the imaged receptor element were contacting each other. The composite was then passed through the hot nip of an IT 6000 hot roll laminator at a speed of 2 feet/minute (~ 1.02 cm/second), at a temperature of 250°F (~ 121°C) and at a pressure of 100 psi (~ 7.0 kg/cm2). Immediately after exiting the nip rolls, the polyethylene terephthlate, temporary carrier layer contiguous to the protective layer was stripped therefrom to form a protected ink image on the vinyl polymer substrate.
Those skilled in the art having the benefit of the teachings of the present invention as hereinabove set forth, can effect numerous modifications thereto. These modifications are to be construed as being encompassed within the scope of the present invention as set forth in the appended claims.

Claims

What is claimed is:
Claim 1.
A process for preparing a protected ink image comprising:
A) imagewise depositing one or more ink images on an ink receptor element, the ink receptor element comprising
1) a temporary carrier layer;
2) an image transparent, protective layer; and
3) an image transparent, ink receptive layer permanently adhered to the protective layer, wherein, the one or more ink images are deposited on the image transparent, ink receptive layer to form an imaged ink receptive layer;
B) applying and adhering to the imaged ink receptive layer to form an imaged laminate, a substrate comprising: a) a support; and b) a first adhesive layer on a first surface of said support, by contacting said substrate to said imaged ink receptive layer, and, C) removing the temporary carrier layer from the image transparent, protective layer of the imaged laminate.
Claim 2.
The process of claim 1 wherein the first adhesive layer is omitted from the substrate and wherein the ink receptive layer includes an adhesive which is activated in step (B) to permanently adhere the imaged ink receptive layer to the substrate.
Claim 3.
The process claim 1 or 2 wherein, the substrate further comprises: c) a second adhesive layer on a second surface of said support opposite said first surface; and optionally, d) a removable cover sheet temporarily adhered to the second adhesive layer; and in performing step (B) the substrate is oriented so that the surface of the substrate bearing the second adhesive layer is away from the imaged ink receptive layer and either before or after step (C), there is performed the additional step:
D) removing the removable cover sheet, if present, from the adhesive layer and adhering the adhesive layer of the imaged laminate to a second substrate to form a mounted, imaged laminate.
Claim 4.
The process of Claim 1 or 2 wherein at least one of the one or more ink images, is imagewise deposited from an ink jet.
Claim 5.
The process of Claim 1 or 2 wherein the substrate is applied to the ink imaged layer under an applied pressure whereby the substrate is permanently adhered to the ink imaged layer of the imaged receptor.
Claim 6.
The process of Claim 1 or 2 wherein the substrate is applied to the ink imaged layer under an applied pressure of atmospheric pressure or greater and at a temperature above room temperature.
Claim 7.
The process of Claim 1 or 2 wherein the substrate is applied to the ink imaged layer at a temperature of about 80°C or greater.
Claim 8.
The process of Claim 7 wherein the substrate is applied to the ink imaged layer at a temperature between about 100°C and about 200°C.
Claim 9.
The process of Claim 1 or 2 wherein the temporary carrier layer is removed from the imaged laminate when the imaged laminate is at a temperature of about 80°C or greater.
Claim 10.
The process of Claim 1 or 2 wherein the temporary carrier layer is a flexible web or sheet material.
Claim 11
The process of Claim 10 wherein the flexible web or sheet material is a polymeric film or a foraminous material.
Claim 12.
The process of Claim 10 wherein the flexible web or sheet material is surface treated with a release agent.
Claim 13.
The process of Claim 1 or 2 wherein the image transparent, protective layer comprises a polymeric film material.
Claim 14.
The process of Claim 13 wherein the polymeric film material is taken from the group consisting of polyvinyl chloride; polyvinylidene chloride; fluorinated polymers and copolymers; polyvinyl butyral; cellulose acetate propionate; cellulose acetate butyrate; polyesters; acrylics; fluorinated polymers; polyurethanes; styrene copolymers; styrene/acrylonitrile copolymers; and combinations thereof.
Claim 15. The process of Claim 1 or 2 wherein the image transparent, protective layer is visually transparent in at least one region within the visible spectral region.
Claim 16. The process of Claim 15 wherein the image transparent, protective layer has a thickness in the range of about 0.5 μm to about 20 μm.
Claim 17. The process of Claim 1 or 2 wherein the image transparent, adhesive, ink receptive layer comprises a hydrophilic resin material.
Claim 18. The process of Claim 17 wherein the hydrophilic resin material comprises a water soluble resin.
Claim 19.
The process of Claim 18 wherein the water soluble resin is polyvinyl pyrrolidone; substituted polyvinyl pyrrolidone; polyvinyl alcohol; substituted polyvinyl alcohol; vinyl pyrrolidone/vinyl acetate copolymer; vinyl acetate/acrylic copolymer; polyacrylic acid; polyacrylamides; hydroxyethylcellulose; carboxyethylcellulose; gelatin; polysaccharides; or mixtures thereof.
Claim 20.
The process of Claim 17 wherein the hydrophilic resin material further comprises a water insoluble resin.
Claim 21.
The process of Claim 20 wherein the water insoluble resin is a styrenated acrylic copolymer; styrene/allyl alcohol copolymer; nitrocellulose; carboxylated resin; polyester resin; polyurethane resin; polyketone resin; polyvinyl butyral resin; or mixtures thereof.
Claim 22.
The process of Claim 1 wherein the first adhesive layer comprises a thermally activated adhesive material.
Claim 23.
The process of Claim 22 wherein the thermally activated adhesive material is a thermoplastic polyurethane, polycaprolactone, acrylic copolymer, a vinyl acetate/acrylic copolymer, or combinations thereof.
Claim 24.
The process of Claim 1 wherein the first adhesive layer comprises a pressure sensitive adhesive material.
Claim 25.
The process of Claim 1 wherein the first adhesive layer comprises a contact adhesive material.
Claim 26.
The process of Claim 1 or 2 wherein the image transparent, ink receptive layer contains a dye mordant, a surfactant, particulate materials, a colorant, an ultraviolet absorbing material, an organic acid, an optical brightener, or mixtures thereof.
Claim 27.
The process of Claim 2 wherein the image transparent, ink --receptive layer comprises a laminate of another adhesive layer and -a iiydrophilic resin layer.
Claim 28.
The process of Claim 27 wherein the other adhesive layer comprises a polycaprolactone material. Claim 29 .
The process of Claim 1 or 2 wherein the substrate is a material taken from the group consisting of wood; metal; ceramic; paper; corrugated paper products; plastics; natural and synthetic fibre fabrics; glasses; leathers; and composites thereof. '
Claim 30.
The process of Claim 1 or 2 wherein the substrate is a flexible web or sheet material.
Claim 31.
The process of Claim 30 wherein the flexible web or sheet material is a polymeric film or a foraminous material.
Claim 32.
The process of Claim 3 wherein after step (C), the image transparent, protective layer along with the image transparent, adhesive, ink receptive layer and the ink imaged layer are removed intact from the substrate and reapplied to the substrate or to a second substrate.
Claim 33.
An ink recording element for use with the process of claim 2 comprising:
1) a temporary carrier layer;
2) an image transparent, protective layer; and
3) an image transparent, adhesive, ink receptive layer permanently adhered to the protective layer; wherein, the image transparent, adhesive, ink receptive layer is receptive to aqueous ink jet inks and comprises a hydrophilic resin material and an adhesive material.
Claim 34. The ink recording element of Claim 33 wherein the adhesive material is a vinyl acetate/ acrylic copolymer.
Claim 35.
The ink recording element of Claim 33 wherein the adhesive material and the hydrophilic resin material are applied as two distinct layers to form the ink receptive layer and wherein the adhesive layer is the upper most layer.
EP94927239A 1993-09-03 1994-09-02 Ink jet imaging process and recording element Expired - Lifetime EP0716633B1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US08/115,561 US5795425A (en) 1993-09-03 1993-09-03 Ink jet imaging process and recording element for use therein
US115564 1993-09-03
US115561 1993-09-03
US08/115,564 US5766398A (en) 1993-09-03 1993-09-03 Ink jet imaging process
PCT/US1994/009644 WO1995006564A1 (en) 1993-09-03 1994-09-02 Ink jet imaging process and recording element

Publications (3)

Publication Number Publication Date
EP0716633A1 true EP0716633A1 (en) 1996-06-19
EP0716633A4 EP0716633A4 (en) 1997-03-05
EP0716633B1 EP0716633B1 (en) 1999-12-08

Family

ID=26813335

Family Applications (1)

Application Number Title Priority Date Filing Date
EP94927239A Expired - Lifetime EP0716633B1 (en) 1993-09-03 1994-09-02 Ink jet imaging process and recording element

Country Status (5)

Country Link
EP (1) EP0716633B1 (en)
JP (1) JPH09503168A (en)
AU (1) AU7674794A (en)
DE (2) DE69422048T2 (en)
WO (1) WO1995006564A1 (en)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6277229B1 (en) 1995-08-25 2001-08-21 Avery Dennison Corporation Image transfer sheets and a method of manufacturing the same
US6824839B1 (en) 1995-08-25 2004-11-30 Avery Dennison Corporation Water-activated polymers and adhesive image transfer technique
US6080261A (en) * 1995-08-25 2000-06-27 Popat; Ghanshyam H. Adhesive image transfer technique
DE29602430U1 (en) * 1996-02-12 1997-07-03 Steinbeis PPL GmbH, 83098 Brannenburg Transfer label
US5681660A (en) * 1996-02-21 1997-10-28 Minnesota Mining And Manufacturing Company Protective clear layer for images
US6153038A (en) * 1996-03-12 2000-11-28 3M Innovative Properties Company Method for transferring an image from a first medium to a second medium at ambient temperature
GB9609443D0 (en) * 1996-05-04 1996-07-10 Brittains Tr Limited Transfers
FR2750080B1 (en) * 1996-06-21 1998-08-28 Dubuit Mach FILM FOR THE HOT DECORATION OF AN OBJECT IN THERMOPLASTIC SYNTHETIC MATERIAL
WO1998015411A1 (en) * 1996-10-08 1998-04-16 Andries Cornelis Pasma Materiel and method for preparing a printed article
EP0865932B1 (en) * 1997-03-18 2002-06-12 Eastman Kodak Company Tamperproof authority document
JP3271931B2 (en) * 1997-05-30 2002-04-08 キヤノン株式会社 Transfer media for inkjet recording
CH692849A5 (en) * 1997-09-15 2002-11-29 Kammann Maschf Werner A method for marking objects.
FR2771675B1 (en) * 1997-12-02 2000-02-11 Thomson Csf PROCESS FOR PRODUCING A SECURE DOCUMENT AND SECURE DOCUMENT OBTAINED BY THIS PROCESS
US6022440A (en) * 1997-12-08 2000-02-08 Imation Corp. Image transfer process for ink-jet generated images
FR2776236B1 (en) * 1998-03-20 2000-05-19 Adhetec COLD DRY TRANSFER, MANUFACTURING METHOD AND APPLICATION METHOD
EP0962829B1 (en) * 1998-06-05 2003-04-23 E.I. Du Pont De Nemours And Company Protective layer for color proofs
ES2212316T3 (en) * 1998-06-30 2004-07-16 Hunt Graphics Europe Limited PRINTED STRATIFICATE.
US20010009174A1 (en) * 1998-07-09 2001-07-26 Duane W Dinkel Inkjet receptor layers on substrates and methods for transferring such layers to such substrates
JP2002525656A (en) * 1998-09-11 2002-08-13 イメイション・コーポレイション Multilayer adhesive bonded article having an ink containing surface bonded to a second surface
JP2002525654A (en) * 1998-09-11 2002-08-13 イメイション・コーポレイション Multilayer article having an ink-containing surface bonded to a second surface by a thermoplastic heat-sealable adhesive
KR20010079787A (en) * 1998-09-11 2001-08-22 윌리엄 데이비드 바우어, 캐씨 로버타 샘스 Multilayer Articles Having Ink-Containing Surface Bonded to a Second Surface with a Photopolymerized Adhesive
ES2152169B1 (en) * 1998-11-11 2001-08-01 Cruz Molina Cristina De PROCEDURE FOR OBTAINING A BODY WITH PRINTED IMAGES AND BODY WITH SUCH PROCEDURE.
US6402316B1 (en) * 1998-12-28 2002-06-11 Canon Kabushiki Kaisha Recording medium, production process of the recording medium, and image forming process using the recording medium
GB9908093D0 (en) * 1999-04-09 1999-06-02 Capital Ind Plc Transfer sheet and method of manufacture
EP1263605B1 (en) 2000-02-08 2005-09-14 3M Innovative Properties Company Improved methods for cold image transfer
DE60112902T2 (en) 2000-02-08 2006-06-14 3M Innovative Properties Co PROCESS AND KIT FOR PROVIDING A CONSISTENT IMAGE ON A SUBSTRATE
JP5105656B2 (en) * 2000-03-22 2012-12-26 萩原工業株式会社 Laminate cloth for inkjet printing and inkjet printing product using the same
GB2362852B (en) * 2000-03-27 2004-02-11 Hewlett Packard Co Photo-media printing using a white backing layer
EP1157852B1 (en) * 2000-05-17 2004-04-14 Du Pont De Nemours (Deutschland) Gmbh Ink receptor sheet and its process of use
US7097298B2 (en) 2000-05-17 2006-08-29 E. I. Du Pont De Nemours And Company Ink receptor sheet and it's process of use
EP1375185A1 (en) * 2000-09-03 2004-01-02 Hewlett-Packard Indigo B.V. Laminated Image Printing
ITVA20000044A1 (en) * 2000-12-22 2002-06-22 Lamberti Spa DECALS FOR CERAMIC OR GLASS USE
US6874421B2 (en) 2001-04-20 2005-04-05 3M Innovative Properties Company Ink jet transfer printing process
JP4342764B2 (en) * 2002-03-22 2009-10-14 株式会社リコー Liquid image forming apparatus
US7625627B2 (en) 2005-12-30 2009-12-01 E.I. Du Pont De Nemours And Company Decorative polyvinyl butyral solar control laminates
US9752022B2 (en) 2008-07-10 2017-09-05 Avery Dennison Corporation Composition, film and related methods
CN105670192A (en) * 2008-07-10 2016-06-15 艾利丹尼森公司 Composition for film and related methods
PL2376289T3 (en) * 2009-01-14 2017-11-30 Mcc-Norwood, Llc Method of making a digitally printed heat transfer label and method of decorating a container using said label
US10328668B1 (en) 2010-02-17 2019-06-25 Mcc-Norwood, Llc Heat transfer label assembly
BR112012022175A2 (en) 2010-03-04 2016-10-25 Avery Dennison Corp non pvc film and non pvc laminate
IN2014CN00656A (en) * 2011-08-02 2015-04-03 3M Innovative Properties Co
JP5944947B2 (en) 2013-08-09 2016-07-05 キヤノンファインテック株式会社 Method for producing transfer body and recorded matter
US20150183544A1 (en) 2013-12-30 2015-07-02 Avery Dennison Corporation Label Application System
JP6366564B2 (en) * 2015-12-08 2018-08-01 キヤノンファインテックニスカ株式会社 Transfer material, recorded matter, production apparatus and production method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3717107A1 (en) * 1986-05-23 1987-11-26 Canon Kk Protective agent for print
US4780348A (en) * 1985-12-03 1988-10-25 Canon Kabushiki Kaisha Print protecting member transfer layer having surface layer with lower softening point than under layer
EP0546650A1 (en) * 1991-12-12 1993-06-16 Eastman Kodak Company Process for the manufacture of self-adhesive pattern

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2622613A1 (en) * 1975-08-22 1977-03-03 Xerox Corp PRINT WHEEL STOP DEVICE
US4165399A (en) * 1975-11-24 1979-08-21 American Can Company Binderless ink for jet printing
JPS54116406A (en) * 1978-02-24 1979-09-10 Dainippon Printing Co Ltd Production of glazed paper
JPS5787397A (en) * 1980-11-19 1982-05-31 Toppan Printing Co Ltd Transfer printing
US4555436A (en) * 1985-09-19 1985-11-26 Dennison Manufacturing Co. Heat transferable laminate
US5120383A (en) * 1986-12-29 1992-06-09 Seiko Epson Corporation Thermal transfer ink sheet and method of printing
GB2210828B (en) * 1987-10-12 1991-09-11 Josiah Wedgwood And Son Limite Transfers and methods of decorating using same
JP2762751B2 (en) * 1991-01-16 1998-06-04 凸版印刷株式会社 Image protection film

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4780348A (en) * 1985-12-03 1988-10-25 Canon Kabushiki Kaisha Print protecting member transfer layer having surface layer with lower softening point than under layer
DE3717107A1 (en) * 1986-05-23 1987-11-26 Canon Kk Protective agent for print
EP0546650A1 (en) * 1991-12-12 1993-06-16 Eastman Kodak Company Process for the manufacture of self-adhesive pattern

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO9506564A1 *

Also Published As

Publication number Publication date
DE69422048T2 (en) 2000-05-31
WO1995006564A1 (en) 1995-03-09
AU7674794A (en) 1995-03-22
DE69422048D1 (en) 2000-01-13
JPH09503168A (en) 1997-03-31
EP0716633B1 (en) 1999-12-08
EP0716633A4 (en) 1997-03-05
DE716633T1 (en) 1996-11-28

Similar Documents

Publication Publication Date Title
EP0716633B1 (en) Ink jet imaging process and recording element
US5766398A (en) Ink jet imaging process
US5795425A (en) Ink jet imaging process and recording element for use therein
US6001482A (en) Ink jet receptor element having a protective layer
KR100494826B1 (en) Thermal transfer compositions, articles and graphic articles made with same
US4440590A (en) Manufacture of signs
US6712532B2 (en) Method of printing film and articles
US20070141328A1 (en) Decorative protective film
CA2234955A1 (en) Ink jet printing sheet
AU4905601A (en) Improved media for cold image transfer
US5162141A (en) Polymeric sheet having an incompatible ink permanently bonded thereto
Brault et al. Ink jet imaging process and recording element for use therein
JP2551408B2 (en) How to decorate items
US5922159A (en) Ink jet imaging layer transfer process
EP0781205B1 (en) Ink jet printing sheet
US20040018345A1 (en) Dry-erase ink marking media
US6911239B2 (en) Recording material and method
EP0900149A1 (en) Decalcomania
JP2001071631A (en) Ink jet recording sheet and its applilcation
EP1188574A2 (en) Recording material and recording method
GB2301693A (en) Transferable signs
CA2057117A1 (en) Polymeric sheet
JP2715274B2 (en) Heat transfer sheet
CA2103280A1 (en) Multilayered printable sheet structure
JP2000001044A (en) Method for ink jet printing and intermediate image receiving medium

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19960220

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR GB

EL Fr: translation of claims filed
DET De: translation of patent claims
A4 Supplementary search report drawn up and despatched

Effective date: 19970114

AK Designated contracting states

Kind code of ref document: A4

Designated state(s): DE FR GB

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

17Q First examination report despatched

Effective date: 19981029

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: REXAM GRAPHICS INC.

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB

REF Corresponds to:

Ref document number: 69422048

Country of ref document: DE

Date of ref document: 20000113

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20020910

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20020911

Year of fee payment: 9

Ref country code: DE

Payment date: 20020911

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030902

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040401

GBPC Gb: european patent ceased through non-payment of renewal fee
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040528

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST