EP1238815A2 - Ink jet recording element and printing method - Google Patents

Ink jet recording element and printing method Download PDF

Info

Publication number
EP1238815A2
EP1238815A2 EP02075736A EP02075736A EP1238815A2 EP 1238815 A2 EP1238815 A2 EP 1238815A2 EP 02075736 A EP02075736 A EP 02075736A EP 02075736 A EP02075736 A EP 02075736A EP 1238815 A2 EP1238815 A2 EP 1238815A2
Authority
EP
European Patent Office
Prior art keywords
recording element
image
ink jet
receiving layer
layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP02075736A
Other languages
German (de)
French (fr)
Other versions
EP1238815A3 (en
Inventor
Lori J. Eastman Kodak Company Shaw-Klein
Alexandra D. Eastman Kodak Company Bermel
Colin Eastman Kodak Company Martin
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.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
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 US09/799,933 external-priority patent/US20020168502A1/en
Priority claimed from US09/799,932 external-priority patent/US6565205B2/en
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Publication of EP1238815A2 publication Critical patent/EP1238815A2/en
Publication of EP1238815A3 publication Critical patent/EP1238815A3/en
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M2205/00Printing methods or features related to printing methods; Location or type of the layers
    • B41M2205/12Preparation of material for subsequent imaging, e.g. corona treatment, simultaneous coating, pre-treatments

Definitions

  • the present invention relates to a porous ink jet recording element and printing method using the element.
  • ink droplets are ejected from a nozzle at high speed towards a recording element or medium to produce an image on the medium.
  • the ink droplets, or recording liquid generally comprise a recording agent, such as a dye or pigment, and a large amount of solvent.
  • the solvent, or carrier liquid typically is made up of water and an organic material such as a monohydric alcohol, a polyhydric alcohol or mixtures thereof.
  • An ink jet recording element typically comprises a support having on at least one surface thereof an ink-receiving or image-receiving layer, and includes those intended for reflection viewing, which have an opaque support, and those intended for viewing by transmitted light, which have a transparent support.
  • porous recording elements have been developed which provide nearly instantaneous drying as long as they have sufficient thickness and pore volume to effectively contain the liquid ink.
  • a porous recording element can be manufactured by cast coating, in which a particulate-containing coating is applied to a support and is dried in contact with a polished smooth surface.
  • EP 1,029,702 discloses an ink jet recording element comprising a support having thereon a gelatin subbing layer and a coating dispersion of silica and PVA.
  • a gelatin subbing layer having thereon a gelatin subbing layer and a coating dispersion of silica and PVA.
  • the gloss is lower than one would like.
  • an ink jet recording element comprising a support having thereon a porous image-receiving layer comprising particles in a binder, the particles having a primary particle size of from 7 to 40 nm in diameter which may be aggregated up to 300 nm, the image-receiving layer being coated from an acidic aqueous dispersion, and the recording element containing a subbing layer between the support and the porous image-receiving layer, the subbing layer comprising a basic material which is capable of raising the surface pH of the image-receiving layer at least 2 pH units.
  • a porous ink jet recording element is obtained that, when printed with dye-based inks, provides better hues and higher gloss.
  • Another preferred embodiment of the invention relates to an ink jet printing method comprising the steps of:
  • the ink-receiving layer of the invention contains particles so that the layer is porous in order to obtain very fast ink drying.
  • the pores formed between the particles must be sufficiently large and interconnected so that the printing ink passes quickly through the layer and away from the outer surface to give the impression of fast drying.
  • the particles must be arranged in such a way so that the pores formed between them are sufficiently small that they do not scatter visible light.
  • the particles may be in the form of primary particles or in the form of secondary aggregated particles.
  • the aggregates are comprised of smaller primary particles 7 to 40 nm in diameter, and being aggregated up to 300 nm in diameter.
  • the pores in a dried coating of such aggregates fall within the range necessary to ensure low optical scatter yet have sufficient ink solvent uptake.
  • the particles useful in the invention may be inorganic or organic and may be manufactured by various methods and are commercially available for an image-receiving layer.
  • particles useful in the invention include alumina, boehmite, clay, calcium carbonate, titanium dioxide, calcined clay, aluminosilicates, silica, barium sulfate, or polymeric beads.
  • the particles may be porous or nonporous.
  • the particles are metallic oxides such as alumina, boehmite or cationically-modified silica.
  • Such particles are preferred because they possess cationic surfaces, which are capable of binding anionic ink jet printing dyes, rendering printed images resistant to dye migration due to water and high humidity conditions.
  • Such particles are considered to possess a cationic charge in aqueous dispersions if the pH of the dispersion is maintained below the particle point of zero charge. The point of zero charge of such particles is above pH 7, so that stable dispersions of such particles are maintained under acidic conditions.
  • stable aqueous dispersions of fumed alumina generally possess a pH of around 4 or lower.
  • the image-receiving layer is coated from an acidic aqueous dispersion having a pH below 5, more preferably at a pH below 4.
  • any basic material may be used in the subbing layer employed in the invention as long as it is compatible with the subbing layer polymer.
  • the basic material comprises sodium hydroxide or triethanolamine.
  • the basic material is capable of raising the surface pH of the image-receiving layer at least above 4.
  • the subbing layer comprises a mixture of a basic material and a polymer.
  • Any polymer may be used in this layer, as long as it is compatible with the basic material.
  • gelatin, poly(vinyl alcohol) or an acrylic latex polymer may be used.
  • the subbing layer comprises from 10-30 % by weight of the basic material.
  • the binder in the image-receiving layer is a hydrophilic polymer such as poly(vinyl alcohol), poly(vinyl pyrrolidone), gelatin, cellulose ethers, poly(oxazolines), poly(vinylacetamides), partially hydrolyzed poly(vinyl acetate/vinyl alcohol), poly(acrylic acid), poly(acrylamide), poly(alkylene oxide), sulfonated or phosphated polyesters and polystyrenes, casein, zein, albumin, chitin, chitosan, dextran, pectin, collagen derivatives, collodian, agar-agar, arrowroot, guar, carrageenan, tragacanth, xanthan, rhamsan and the like.
  • hydrophilic polymer such as poly(vinyl alcohol), poly(vinyl pyrrolidone), gelatin, cellulose ethers, poly(oxazolines), poly(vinylacetamides
  • the hydrophilic polymer is poly(vinyl alcohol), hydroxypropyl cellulose, hydroxypropyl methyl cellulose, gelatin, or a poly(alkylene oxide).
  • the hydrophilic binder is poly(vinyl alcohol). The binder should be chosen so that it is compatible with the aforementioned particles.
  • the amount of binder used should be sufficient to impart cohesive strength to the ink jet recording element, but should also be minimized so that the interconnected pore structure formed by the aggregates is not filled in by the binder.
  • the weight ratio of the binder to the total amount of particles is from 1:20 to 1:5.
  • the void volume must be sufficient to absorb all of the printing ink. For example, if a porous layer has 60 volume % open pores, in order to instantly absorb 32 cc/m 2 of ink, it must have a physical thickness of at least 54 ⁇ m.
  • the support for the ink jet recording element used in the invention can be any of those usually used for ink jet receivers, such as resin-coated paper, paper, polyesters, or microporous materials such as polyethylene polymer-containing material sold by PPG Industries, Inc., Pittsburgh, Pennsylvania under the trade name of Teslin ®, Tyvek ® synthetic paper (DuPont Corp.), and OPPalyte® films (Mobil Chemical Co.) and other composite films listed in U.S. Patent 5,244,861.
  • Opaque supports include plain paper, coated paper, synthetic paper, photographic paper support, melt-extrusion-coated paper, and laminated paper, such as biaxially oriented support laminates. Biaxially oriented support laminates are described in U.S.
  • biaxially oriented supports include a paper base and a biaxially oriented polyolefin sheet, typically polypropylene, laminated to one or both sides of the paper base.
  • Transparent supports include glass, cellulose derivatives, e.g., a cellulose ester, cellulose triacetate, cellulose diacetate, cellulose acetate propionate, cellulose acetate butyrate; polyesters, such as poly(ethylene terephthalate), poly(ethylene naphthalate), poly(1,4-cyclohexanedimethylene terephthalate), poly(butylene terephthalate), and copolymers thereof; polyimides; polyamides; polycarbonates; polystyrene; polyolefins, such as polyethylene or polypropylene; polysulfones; polyacrylates; polyetherimides; and mixtures thereof.
  • the papers listed above include a broad range of papers, from high end papers, such as photographic paper to low end papers, such as newsprint. In a preferred embodiment, polyethylene-coated paper is employed.
  • the support used in the invention may have a thickness of from 50 to 500 ⁇ m, preferably from 75 to 300 ⁇ m.
  • Antioxidants, antistatic agents, plasticizers and other known additives may be incorporated into the support, if desired.
  • the surface of the support may be subjected to a corona-discharge treatment prior to applying the image-receiving layer.
  • Coating compositions employed in the invention may be applied by any number of well known techniques, including dip-coating, wound-wire rod coating, doctor blade coating, gravure and reverse-roll coating, slide coating, bead coating, extrusion coating, curtain coating and the like.
  • Known coating and drying methods are described in further detail in Research Disclosure no. 308119, published Dec. 1989, pages 1007 to 1008.
  • Slide coating is preferred, in which the image-receiving layer and an overcoat layer may be simultaneously applied.
  • the layers are generally dried by simple evaporation, which may be accelerated by known techniques such as convection heating.
  • crosslinkers which act upon the binder discussed above may be added in small quantities. Such an additive improves the cohesive strength of the layer.
  • Crosslinkers such as carbodiimides, polyfunctional aziridines, aldehydes, isocyanates, epoxides, polyvalent metal cations, and the like may all be used.
  • UV absorbers may also be added to the image-receiving layer as is well known in the art.
  • Other additives include adhesion promoters, rheology modifiers, surfactants, biocides, lubricants, dyes, optical brighteners, matte agents, antistatic agents, etc.
  • additives known to those familiar with such art such as surfactants, defoamers, alcohol and the like may be used.
  • a common level for coating aids is 0.01 to 0.30 % active coating aid based on the total solution weight.
  • These coating aids can be nonionic, anionic, cationic or amphoteric. Specific examples are described in MCCUTCHEON's Volume 1: Emulsifiers and Detergents, 1995, North American Edition.
  • the coating composition can be coated so that the total solids content will yield a useful coating thickness, and for particulate coating formulations, solids contents from 10-60% are typical.
  • the ink jet inks used to image the recording elements of the present invention are well-known in the art.
  • the ink compositions used in ink jet printing typically are liquid compositions comprising a solvent or carrier liquid, dyes or pigments, humectants, organic solvents, detergents, thickeners, preservatives, and the like.
  • the solvent or carrier liquid can be solely water or can be water mixed with other water-miscible solvents such as polyhydric alcohols.
  • Inks in which organic materials such as polyhydric alcohols are the predominant carrier or solvent liquid may also be used. Particularly useful are mixed solvents of water and polyhydric alcohols.
  • the dyes used in such compositions are typically watersoluble direct or acid type dyes.
  • Such liquid compositions have been described extensively in the prior art including, for example, U.S. Patents 4,381,946; 4,239,543 and 4,781,758.
  • a basic subbing layer was prepared by combining lime-process ossein photographic grade gelatin (Eastman Gelatine) and sodium hydroxide (Aldrich Chemical Co.) in a ratio of 4.3:1 to give an aqueous coating solution of 3 % solids.
  • the above coating solution was bead-coated at 40 °C on a polyethylene-coated paper base which had been previously subjected to a corona discharge treatment.
  • the coating was then dried at 60°C by forced air to yield a basic subbing layer having a thickness of 1.5 ⁇ m, or a dry coating weight of 1.6 g/m 2 .
  • the ink jet receiving layers were prepared as follows: A coating solution for a bottom ink absorbing layer was prepared by combining fumed alumina (Cab-O-Sperse® PG003, Cabot Corp.), poly(vinyl alcohol) (Gohsenol® GH-23A, Nippon Gohsei Co., Ltd.) and 2,3-dihydroxy-1,4-dioxane (Clariant Corp.) in a ratio of 88:10:2 to give an aqueous coating formulation of 30% solids by weight.
  • fumed alumina Cab-O-Sperse® PG003, Cabot Corp.
  • poly(vinyl alcohol) Gohsenol® GH-23A, Nippon Gohsei Co., Ltd.
  • 2,3-dihydroxy-1,4-dioxane Clariant Corp.
  • a coating solution for an overcoat layer was prepared by combining fumed alumina (Cab-O-Sperse® PG003, Cabot Corp.), poly(vinyl alcohol) (Gohsenol® GH-23A, Nippon Gohsei Co.) and a copolymer of (vinylbenzyl)trimethyl-ammonium chloride and divinylbenzene (87:13 molar ratio) in a ratio of 85:3:12 to give an aqueous coating formulation of 10% solids by weight.
  • Surfactants Zonyl® FSN (E. I. du Pont de Nemours and Co.) and Olin® 10G (Dixie Chemical Co.) were added in small amounts as coating aids.
  • the above coating solutions were simultaneously bead-coated at 40° C on the basic subbing layer described above.
  • the overcoat layer was coated on top of the bottom ink-absorbing layer.
  • the coating was then dried at 60 ° C by forced air to yield a two-layer recording element in which the thicknesses of the bottom and topmost layers were 40 ⁇ m (43 g/m 2 ) and 2 ⁇ m (2.2 g/m 2 ), respectively.
  • Element 2 was prepared the same as Element 1 except that the basic subbing layer comprised a combination of poly(vinyl alcohol) (Gohsenol® GH-23A, Nippon Gohsei Co.) and triethanolamine in a ratio of 4.3:1:
  • the basic subbing layer comprised a combination of poly(vinyl alcohol) (Gohsenol® GH-23A, Nippon Gohsei Co.) and triethanolamine in a ratio of 4.3:1:
  • Element 3 was prepared the same as Element 1 except that the basic subbing layer comprised a combination of an acrylic latex (Neocryl® A622, Zeneca Resins) and sodium hydroxide in a ratio of 4.3:1.
  • an acrylic latex Naeocryl® A622, Zeneca Resins
  • sodium hydroxide sodium hydroxide
  • This element was prepared the same as Element 1 except that no basic subbing layer was coated.
  • This element was prepared the same as Element 1 except that the subbing layer comprised only gelatin. No basic material was added.
  • This element was prepared the same as Control Element 1 except that sodium hydroxide was added to the overcoat coating solution during the bead coating process by simultaneously adding an aqueous solution of sodium hydroxide into the top slot of the coating hopper. A dried coating could not be obtained due to severe flocculation of the coating melt before it could be successfully deposited onto the support.
  • the dried coatings were evaluated visually for surface appearance, primarily cracking.
  • the gloss of each coating was measured at angles of 20 and 60 degrees from the perpendicular to the coating surface using a BYK Gardner microgloss meter.
  • the surface pH of each dried coating was measured using a conventional surface pH marking pencil (pHydrion Insta-chek® Gardco Co.). The following results were obtained: Recording Element Appearance 20 degree gloss 60 degree gloss pH 1 Fair 32 68 4.5 2 Excellent 34 71 4.0 3 Fair 32 69 5.0 C-1 Excellent 32 68 2.0 C-2 Severely cracked 2 9 2.5 C-4 Excellent 13 32 5.0
  • Test images of a cyan patch at 100% ink laydown were printed using an Epson Stylus® Photo 870 using inks with catalogue number T008201.

Abstract

An ink jet recording element and printing method using the element, comprising a support having thereon a porous image-receiving layer comprising particles in a binder, the particles having a primary particle size of from 7 to 40 nm in diameter which may be aggregated up to 300 nm, the image-receiving layer being coated from an acidic aqueous dispersion, and the recording element containing a subbing layer between the support and the porous image-receiving layer, the subbing layer comprising a basic material which is capable of raising the surface pH of the image-receiving layer at least 2 pH units.

Description

  • The present invention relates to a porous ink jet recording element and printing method using the element.
  • In a typical ink jet recording or printing system, ink droplets are ejected from a nozzle at high speed towards a recording element or medium to produce an image on the medium. The ink droplets, or recording liquid, generally comprise a recording agent, such as a dye or pigment, and a large amount of solvent. The solvent, or carrier liquid, typically is made up of water and an organic material such as a monohydric alcohol, a polyhydric alcohol or mixtures thereof.
  • An ink jet recording element typically comprises a support having on at least one surface thereof an ink-receiving or image-receiving layer, and includes those intended for reflection viewing, which have an opaque support, and those intended for viewing by transmitted light, which have a transparent support.
  • An important characteristic of ink jet recording elements is their need to dry quickly after printing. To this end, porous recording elements have been developed which provide nearly instantaneous drying as long as they have sufficient thickness and pore volume to effectively contain the liquid ink. For example, a porous recording element can be manufactured by cast coating, in which a particulate-containing coating is applied to a support and is dried in contact with a polished smooth surface.
  • EP 1,029,702 discloses an ink jet recording element comprising a support having thereon a gelatin subbing layer and a coating dispersion of silica and PVA. However, there is a problem with this element in that the gloss is lower than one would like.
  • It is an object of this invention to provide a porous ink jet recording element that, when printed with dye-based inks, provides better hues and higher gloss. It is another object of this invention to provide a porous ink jet recording element that has an acid-free surface, which is desirable for archival printing applications. Still another object of the invention is to provide a printing method using the above-described element.
  • These and other objects are achieved in accordance with the invention which comprises an ink jet recording element comprising a support having thereon a porous image-receiving layer comprising particles in a binder, the particles having a primary particle size of from 7 to 40 nm in diameter which may be aggregated up to 300 nm, the image-receiving layer being coated from an acidic aqueous dispersion, and the recording element containing a subbing layer between the support and the porous image-receiving layer, the subbing layer comprising a basic material which is capable of raising the surface pH of the image-receiving layer at least 2 pH units.
  • By use of the invention, a porous ink jet recording element is obtained that, when printed with dye-based inks, provides better hues and higher gloss.
  • Another preferred embodiment of the invention relates to an ink jet printing method comprising the steps of:
  • A) providing an ink jet printer that is responsive to digital data signals;
  • B) loading the printer with an ink jet recording element comprising the element described above;
  • C) loading the printer with an ink jet ink composition; and
  • D) printing on the image-receiving layer using the ink jet ink composition in response to the digital data signals.
  • The ink-receiving layer of the invention contains particles so that the layer is porous in order to obtain very fast ink drying. The pores formed between the particles must be sufficiently large and interconnected so that the printing ink passes quickly through the layer and away from the outer surface to give the impression of fast drying. At the same time, the particles must be arranged in such a way so that the pores formed between them are sufficiently small that they do not scatter visible light.
  • The particles may be in the form of primary particles or in the form of secondary aggregated particles. The aggregates are comprised of smaller primary particles 7 to 40 nm in diameter, and being aggregated up to 300 nm in diameter. The pores in a dried coating of such aggregates fall within the range necessary to ensure low optical scatter yet have sufficient ink solvent uptake. The particles useful in the invention may be inorganic or organic and may be manufactured by various methods and are commercially available for an image-receiving layer.
  • Examples of particles useful in the invention include alumina, boehmite, clay, calcium carbonate, titanium dioxide, calcined clay, aluminosilicates, silica, barium sulfate, or polymeric beads. The particles may be porous or nonporous. In a preferred embodiment of the invention, the particles are metallic oxides such as alumina, boehmite or cationically-modified silica. Such particles are preferred because they possess cationic surfaces, which are capable of binding anionic ink jet printing dyes, rendering printed images resistant to dye migration due to water and high humidity conditions. Such particles are considered to possess a cationic charge in aqueous dispersions if the pH of the dispersion is maintained below the particle point of zero charge. The point of zero charge of such particles is above pH 7, so that stable dispersions of such particles are maintained under acidic conditions. For example, stable aqueous dispersions of fumed alumina generally possess a pH of around 4 or lower.
  • In a preferred embodiment of the invention, the image-receiving layer is coated from an acidic aqueous dispersion having a pH below 5, more preferably at a pH below 4.
  • Any basic material may be used in the subbing layer employed in the invention as long as it is compatible with the subbing layer polymer. In a preferred embodiment, the basic material comprises sodium hydroxide or triethanolamine. In another preferred embodiment, the basic material is capable of raising the surface pH of the image-receiving layer at least above 4.
  • In yet another preferred embodiment of the invention, the subbing layer comprises a mixture of a basic material and a polymer. Any polymer may be used in this layer, as long as it is compatible with the basic material. For example, gelatin, poly(vinyl alcohol) or an acrylic latex polymer may be used.
  • While any amount of basic material may be used in the subbing layer, in general, the subbing layer comprises from 10-30 % by weight of the basic material.
  • In a preferred embodiment of the invention, the binder in the image-receiving layer is a hydrophilic polymer such as poly(vinyl alcohol), poly(vinyl pyrrolidone), gelatin, cellulose ethers, poly(oxazolines), poly(vinylacetamides), partially hydrolyzed poly(vinyl acetate/vinyl alcohol), poly(acrylic acid), poly(acrylamide), poly(alkylene oxide), sulfonated or phosphated polyesters and polystyrenes, casein, zein, albumin, chitin, chitosan, dextran, pectin, collagen derivatives, collodian, agar-agar, arrowroot, guar, carrageenan, tragacanth, xanthan, rhamsan and the like. In still another preferred embodiment of the invention, the hydrophilic polymer is poly(vinyl alcohol), hydroxypropyl cellulose, hydroxypropyl methyl cellulose, gelatin, or a poly(alkylene oxide). In yet still another preferred embodiment, the hydrophilic binder is poly(vinyl alcohol). The binder should be chosen so that it is compatible with the aforementioned particles.
  • The amount of binder used should be sufficient to impart cohesive strength to the ink jet recording element, but should also be minimized so that the interconnected pore structure formed by the aggregates is not filled in by the binder. In a preferred embodiment of the invention, the weight ratio of the binder to the total amount of particles is from 1:20 to 1:5.
  • Since the image-receiving layer is a porous layer comprising particles, the void volume must be sufficient to absorb all of the printing ink. For example, if a porous layer has 60 volume % open pores, in order to instantly absorb 32 cc/m2 of ink, it must have a physical thickness of at least 54 µm.
  • The support for the ink jet recording element used in the invention can be any of those usually used for ink jet receivers, such as resin-coated paper, paper, polyesters, or microporous materials such as polyethylene polymer-containing material sold by PPG Industries, Inc., Pittsburgh, Pennsylvania under the trade name of Teslin ®, Tyvek ® synthetic paper (DuPont Corp.), and OPPalyte® films (Mobil Chemical Co.) and other composite films listed in U.S. Patent 5,244,861. Opaque supports include plain paper, coated paper, synthetic paper, photographic paper support, melt-extrusion-coated paper, and laminated paper, such as biaxially oriented support laminates. Biaxially oriented support laminates are described in U.S. Patents 5,853,965; 5,866,282; 5,874,205; 5,888,643; 5,888,681; 5,888,683; and 5,888,714. These biaxially oriented supports include a paper base and a biaxially oriented polyolefin sheet, typically polypropylene, laminated to one or both sides of the paper base. Transparent supports include glass, cellulose derivatives, e.g., a cellulose ester, cellulose triacetate, cellulose diacetate, cellulose acetate propionate, cellulose acetate butyrate; polyesters, such as poly(ethylene terephthalate), poly(ethylene naphthalate), poly(1,4-cyclohexanedimethylene terephthalate), poly(butylene terephthalate), and copolymers thereof; polyimides; polyamides; polycarbonates; polystyrene; polyolefins, such as polyethylene or polypropylene; polysulfones; polyacrylates; polyetherimides; and mixtures thereof. The papers listed above include a broad range of papers, from high end papers, such as photographic paper to low end papers, such as newsprint. In a preferred embodiment, polyethylene-coated paper is employed.
  • The support used in the invention may have a thickness of from 50 to 500 µm, preferably from 75 to 300 µm. Antioxidants, antistatic agents, plasticizers and other known additives may be incorporated into the support, if desired.
  • In order to improve the adhesion of the ink-receiving layer to the support, the surface of the support may be subjected to a corona-discharge treatment prior to applying the image-receiving layer.
  • Coating compositions employed in the invention may be applied by any number of well known techniques, including dip-coating, wound-wire rod coating, doctor blade coating, gravure and reverse-roll coating, slide coating, bead coating, extrusion coating, curtain coating and the like. Known coating and drying methods are described in further detail in Research Disclosure no. 308119, published Dec. 1989, pages 1007 to 1008. Slide coating is preferred, in which the image-receiving layer and an overcoat layer may be simultaneously applied. After coating, the layers are generally dried by simple evaporation, which may be accelerated by known techniques such as convection heating.
  • In order to impart mechanical durability to an ink jet recording element, crosslinkers which act upon the binder discussed above may be added in small quantities. Such an additive improves the cohesive strength of the layer. Crosslinkers such as carbodiimides, polyfunctional aziridines, aldehydes, isocyanates, epoxides, polyvalent metal cations, and the like may all be used.
  • To improve colorant fade, UV absorbers, radical quenchers or antioxidants may also be added to the image-receiving layer as is well known in the art. Other additives include adhesion promoters, rheology modifiers, surfactants, biocides, lubricants, dyes, optical brighteners, matte agents, antistatic agents, etc. In order to obtain adequate coatability, additives known to those familiar with such art such as surfactants, defoamers, alcohol and the like may be used. A common level for coating aids is 0.01 to 0.30 % active coating aid based on the total solution weight. These coating aids can be nonionic, anionic, cationic or amphoteric. Specific examples are described in MCCUTCHEON's Volume 1: Emulsifiers and Detergents, 1995, North American Edition.
  • The coating composition can be coated so that the total solids content will yield a useful coating thickness, and for particulate coating formulations, solids contents from 10-60% are typical.
  • Ink jet inks used to image the recording elements of the present invention are well-known in the art. The ink compositions used in ink jet printing typically are liquid compositions comprising a solvent or carrier liquid, dyes or pigments, humectants, organic solvents, detergents, thickeners, preservatives, and the like. The solvent or carrier liquid can be solely water or can be water mixed with other water-miscible solvents such as polyhydric alcohols. Inks in which organic materials such as polyhydric alcohols are the predominant carrier or solvent liquid may also be used. Particularly useful are mixed solvents of water and polyhydric alcohols. The dyes used in such compositions are typically watersoluble direct or acid type dyes. Such liquid compositions have been described extensively in the prior art including, for example, U.S. Patents 4,381,946; 4,239,543 and 4,781,758.
  • The following example is provided to illustrate the invention.
  • Element 1 of the Invention
  • A basic subbing layer was prepared by combining lime-process ossein photographic grade gelatin (Eastman Gelatine) and sodium hydroxide (Aldrich Chemical Co.) in a ratio of 4.3:1 to give an aqueous coating solution of 3 % solids. The above coating solution was bead-coated at 40 °C on a polyethylene-coated paper base which had been previously subjected to a corona discharge treatment. The coating was then dried at 60°C by forced air to yield a basic subbing layer having a thickness of 1.5 µm, or a dry coating weight of 1.6 g/m2.
  • The ink jet receiving layers were prepared as follows: A coating solution for a bottom ink absorbing layer was prepared by combining fumed alumina (Cab-O-Sperse® PG003, Cabot Corp.), poly(vinyl alcohol) (Gohsenol® GH-23A, Nippon Gohsei Co., Ltd.) and 2,3-dihydroxy-1,4-dioxane (Clariant Corp.) in a ratio of 88:10:2 to give an aqueous coating formulation of 30% solids by weight.
  • A coating solution for an overcoat layer was prepared by combining fumed alumina (Cab-O-Sperse® PG003, Cabot Corp.), poly(vinyl alcohol) (Gohsenol® GH-23A, Nippon Gohsei Co.) and a copolymer of (vinylbenzyl)trimethyl-ammonium chloride and divinylbenzene (87:13 molar ratio) in a ratio of 85:3:12 to give an aqueous coating formulation of 10% solids by weight. Surfactants Zonyl® FSN (E. I. du Pont de Nemours and Co.) and Olin® 10G (Dixie Chemical Co.) were added in small amounts as coating aids.
  • The above coating solutions were simultaneously bead-coated at 40° C on the basic subbing layer described above. The overcoat layer was coated on top of the bottom ink-absorbing layer. The coating was then dried at 60 ° C by forced air to yield a two-layer recording element in which the thicknesses of the bottom and topmost layers were 40 µm (43 g/m2) and 2 µm (2.2 g/m2), respectively.
  • Element 2 of the Invention
  • Element 2 was prepared the same as Element 1 except that the basic subbing layer comprised a combination of poly(vinyl alcohol) (Gohsenol® GH-23A, Nippon Gohsei Co.) and triethanolamine in a ratio of 4.3:1:
  • Element 3 of the Invention
  • Element 3 was prepared the same as Element 1 except that the basic subbing layer comprised a combination of an acrylic latex (Neocryl® A622, Zeneca Resins) and sodium hydroxide in a ratio of 4.3:1.
  • Control Element 1
  • This element was prepared the same as Element 1 except that no basic subbing layer was coated.
  • Control Element 2
  • This element was prepared the same as Element 1 except that the subbing layer comprised only gelatin. No basic material was added.
  • Control Element 3
  • This element was prepared the same as Control Element 1 except that sodium hydroxide was added to the overcoat coating solution during the bead coating process by simultaneously adding an aqueous solution of sodium hydroxide into the top slot of the coating hopper. A dried coating could not be obtained due to severe flocculation of the coating melt before it could be successfully deposited onto the support.
  • Control Element 4
  • For reference, a commercially available inkjet receiver was used. (Epson ® Professional Media Photo Glossy Paper, catalog number SP91001).
  • Coating Quality
  • The dried coatings were evaluated visually for surface appearance, primarily cracking. The gloss of each coating was measured at angles of 20 and 60 degrees from the perpendicular to the coating surface using a BYK Gardner microgloss meter. The surface pH of each dried coating was measured using a conventional surface pH marking pencil (pHydrion Insta-chek® Gardco Co.). The following results were obtained:
    Recording Element Appearance 20 degree gloss 60 degree gloss pH
    1 Fair 32 68 4.5
    2 Excellent 34 71 4.0
    3 Fair 32 69 5.0
    C-1 Excellent 32 68 2.0
    C-2 Severely cracked 2 9 2.5
    C-4 Excellent 13 32 5.0
  • The above results show that the surface pH of the coating of the Elements of the invention was raised from the level of C-1 while maintaining high gloss and having an acceptable appearance. In contrast thereto, C-2 was severely cracked and had low gloss while C-4 also had low gloss.
  • Density Testing
  • Test images of a cyan patch at 100% ink laydown were printed using an Epson Stylus® Photo 870 using inks with catalogue number T008201.
  • After drying for 24 hours at ambient temperature and humidity, the colorimetry of the cyan patch was measured using a Minolta colorimeter. The a* and b* values describe the hue of the patch. More negative a* values represent a more green hue, while more negative b* values represent more blue color. The following results were obtained:
    Recording Element a* b*
    1 -26.37 -57.76
    2 -30.81 -52.77
    3 -26.62 -57.17
    C-1 -36.59 -46.38
    C-4 -34.61 -56.26
  • The above results show that the cyan patch appears bluer (b* values more negative) for the recording elements of the invention as compared to C-1 which was not pH adjusted. (C-4 has an acceptable blueness which was used as a standard).

Claims (10)

  1. An ink jet recording element comprising a support having thereon a porous image-receiving layer comprising particles in a binder, said particles having a primary particle size of from 7 to 40 nm in diameter which may be aggregated up to 300 nm, said image-receiving layer being coated from an acidic aqueous dispersion, and said recording element containing a subbing layer between said support and said porous image-receiving layer, said subbing layer comprising a basic material which is capable of raising the surface pH of said image-receiving layer at least 2 pH units.
  2. The recording element of Claim 1 wherein said image-receiving layer being coated from an acidic aqueous dispersion having a pH below 5.
  3. The recording element of Claim 1 wherein said image-receiving layer being coated from an acidic aqueous dispersion having a pH below 4.
  4. The recording element of Claim 1 wherein said basic material is capable of raising the surface pH of said image-receiving layer at least above 4.
  5. The recording element of Claim 1 wherein said subbing layer comprises a mixture of a polymer and a basic material.
  6. The recording element of Claim 5 wherein said polymer is gelatin, poly(vinyl alcohol) or an acrylic latex polymer.
  7. The recording element of Claim 5 wherein said basic material comprises sodium hydroxide or triethanolamine.
  8. The recording element of Claim 1 wherein said subbing layer comprises from 10-30 % by weight of said basic material.
  9. The recording element of Claim 1 wherein said binder is a hydrophilic polymer.
  10. An ink jet printing method, comprising the steps of:
    A) providing an ink jet printer that is responsive to digital data signals;
    B) loading said printer with an ink jet recording element comprising the element as described in Claim 1;
    C) loading said printer with an ink jet ink composition; and
    D) printing on said image-receiving layer using said ink jet ink composition in response to said digital data signals.
EP02075736A 2001-03-06 2002-02-22 Ink jet recording element and printing method Withdrawn EP1238815A3 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US799933 2001-03-06
US09/799,933 US20020168502A1 (en) 2001-03-06 2001-03-06 Ink jet recording element
US799932 2001-03-06
US09/799,932 US6565205B2 (en) 2001-03-06 2001-03-06 Ink jet printing method

Publications (2)

Publication Number Publication Date
EP1238815A2 true EP1238815A2 (en) 2002-09-11
EP1238815A3 EP1238815A3 (en) 2003-11-19

Family

ID=27122169

Family Applications (1)

Application Number Title Priority Date Filing Date
EP02075736A Withdrawn EP1238815A3 (en) 2001-03-06 2002-02-22 Ink jet recording element and printing method

Country Status (2)

Country Link
EP (1) EP1238815A3 (en)
JP (1) JP2002331746A (en)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5853965A (en) 1997-05-23 1998-12-29 Eastman Kodak Company Photographic element with bonding layer on oriented sheet
US5866282A (en) 1997-05-23 1999-02-02 Eastman Kodak Company Composite photographic material with laminated biaxially oriented polyolefin sheets
US5874205A (en) 1997-05-23 1999-02-23 Eastman Kodak Company Photographic element with indicia on oriented polymer back sheet
US5888643A (en) 1997-05-23 1999-03-30 Eastman Kodak Company Controlling bending stiffness in photographic paper
US5888714A (en) 1997-12-24 1999-03-30 Eastman Kodak Company Adhesives such as metallocene catalyzed ethylene plastomers for bonding biaxially oriented polyolefin sheets to paper
US5888681A (en) 1997-05-23 1999-03-30 Eastman Kodak Company Photographic element with microvoided sheet of opalescent appearance
US5888683A (en) 1997-05-23 1999-03-30 Eastman Kodak Company Roughness elimination by control of strength of polymer sheet in relation to base paper
EP1029702A2 (en) 1999-02-15 2000-08-23 Konica Corporation Surface treatment method, production method for ink jet recording medium, and ink jet recording medium

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69402573T2 (en) * 1993-02-01 1997-11-27 Agfa Gevaert Nv Ink receiving layers
EP0609930B1 (en) * 1993-02-01 1997-04-16 Agfa-Gevaert N.V. Ink-receiving layers
US5439739A (en) * 1993-06-03 1995-08-08 Mitsubishi Paper Mills Limited Ink jet recording medium
JPH11271927A (en) * 1998-01-20 1999-10-08 Mitsubishi Paper Mills Ltd Supporting body for image material
EP1002660B1 (en) * 1998-06-10 2006-08-30 Konica Minolta Holdings, Inc. Ink-jet recording paper

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5853965A (en) 1997-05-23 1998-12-29 Eastman Kodak Company Photographic element with bonding layer on oriented sheet
US5866282A (en) 1997-05-23 1999-02-02 Eastman Kodak Company Composite photographic material with laminated biaxially oriented polyolefin sheets
US5874205A (en) 1997-05-23 1999-02-23 Eastman Kodak Company Photographic element with indicia on oriented polymer back sheet
US5888643A (en) 1997-05-23 1999-03-30 Eastman Kodak Company Controlling bending stiffness in photographic paper
US5888681A (en) 1997-05-23 1999-03-30 Eastman Kodak Company Photographic element with microvoided sheet of opalescent appearance
US5888683A (en) 1997-05-23 1999-03-30 Eastman Kodak Company Roughness elimination by control of strength of polymer sheet in relation to base paper
US5888714A (en) 1997-12-24 1999-03-30 Eastman Kodak Company Adhesives such as metallocene catalyzed ethylene plastomers for bonding biaxially oriented polyolefin sheets to paper
EP1029702A2 (en) 1999-02-15 2000-08-23 Konica Corporation Surface treatment method, production method for ink jet recording medium, and ink jet recording medium

Also Published As

Publication number Publication date
EP1238815A3 (en) 2003-11-19
JP2002331746A (en) 2002-11-19

Similar Documents

Publication Publication Date Title
US6689430B2 (en) Ink jet recording element
US6641875B2 (en) Ink jet recording element
US6419355B1 (en) Ink jet printing method
US6447110B1 (en) Ink jet printing method
US6630212B2 (en) Ink jet recording element
EP1288012B1 (en) Ink jet recording element and printing method
US6443570B1 (en) Ink jet printing method
US6565205B2 (en) Ink jet printing method
EP1386751A2 (en) Ink jet recording element and printing method
EP1226970B1 (en) Ink jet recording element and printing method
US6547386B2 (en) Ink jet printing method
EP1288011B1 (en) Ink jet recording element and printing method
EP1226962B1 (en) Ink jet recording element and printing method
EP1319516B1 (en) Ink jet recording element and printing method
EP1288008B1 (en) Ink jet recording element and printing method
US20020140792A1 (en) Ink jet printing method
US20020168502A1 (en) Ink jet recording element
US6548151B2 (en) Ink jet recording element
EP1238815A2 (en) Ink jet recording element and printing method
US6431701B1 (en) Ink jet printing method
US6815020B2 (en) Ink jet recording element
US6623831B2 (en) Ink jet printing method
US20030108691A1 (en) Ink jet printing method
US20030137574A1 (en) Ink jet printing method
EP1319517A1 (en) Ink jet recording element and printing method

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

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

AKX Designation fees paid
REG Reference to a national code

Ref country code: DE

Ref legal event code: 8566

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

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20040520