EP0976571A1 - Porous inkjet recording elements - Google Patents
Porous inkjet recording elements Download PDFInfo
- Publication number
- EP0976571A1 EP0976571A1 EP99202390A EP99202390A EP0976571A1 EP 0976571 A1 EP0976571 A1 EP 0976571A1 EP 99202390 A EP99202390 A EP 99202390A EP 99202390 A EP99202390 A EP 99202390A EP 0976571 A1 EP0976571 A1 EP 0976571A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- inkjet recording
- recording medium
- coating composition
- coating
- silica
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5218—Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays
Definitions
- This invention relates to an ink receptive material comprising a support material containing at least one layer consisting essentailly of a mixture of inorganic particles; specifically a mixture of colloidal ( ⁇ 1 micron) and noncolloidal inorganic particulates.
- Ink receptive materials for inkjet printing or other liquid marking processes typically employ layers comprising materials which are particularly receptive to the solvent or carrier making up the ink.
- the ink receiving layer could be comprised of a hydrophilic material so that the capacity of the receiving layer to swell in the ink solvent allows the printed areas to become quickly apparently dry and also prevents flooding of the ink on the surface.
- the ink receiving layer could be comprised primarily of particulate materials so that the coated layer is highly porous and is therefore able to carry the ink away from the printed surface quickly.
- primarily particulate material it is meant that most (over 50%) of the volume of the image receptive layer comprises distinct particles, either never in solution or precipitated during the coating process. This alternative would also give the impression of fast drying and would limit any flooding of the surface in areas of high ink deposit.
- the porous coating approach is preferred as it is inexpensive and easily applied by common coating methods such as gravure coating.
- the particles which make up such a porous coating can be polymeric or inorganic, and may have a hydrophilic character. Such particles, when used for paper coatings, are typically referred to as pigments.
- polymeric binders are added to the coating formulation. They act like glue to help adhere the particles to each other and to the coated support.
- these polymers are solution polymers such as polyvinyl alcohol or casein; or latex polymers such as styrene-butadiene or acrylonitrile-styrene-butadiene. If a latex polymer is preferred over a solution polymer as a binder, typically more latex is necessary in order to obtain sufficient cohesive strength in the layer.
- a further addition to such a coating formulation or an additional overcoat is typically a crosslinker capable of cross linking the hydroxyl or carboxyl groups introduced by the polymeric binder. This cross linking provides additional water resistance to the coating.
- polymeric mordants are often added to such ink receiving layers in order to impart waterfastness to the printing inks.
- US 5,616,409 describes an inkjet recording medium comprising a paper of defined density and Stockigt sizing degree over which an ink receptive layer has been coated.
- the coated layers comprise 75% pigment, 20% binder and 5% cationic polymeric mordant.
- the pigment consists of porous synthetic amorphous silica powder with particle sizes over 1 micron, and the binder is either polyvinyl alcohol or silanol-modified vinyl alcohol
- EP Application 0 754 560 describes a color inkjet recording sheet which is coated from an aqueous formulation containing a water-soluble crosslinkable polymeric binder, an absorptive pigment, a zirconium crosslinking agent, and a cationically modified polymer.
- Binder examples include water soluble polymers such as polyvinyl alcohol, hydroxyethyl cellulose and rice starch.
- the binder concentration, as a percent of total pigment+binder content, ranges from 12.7% to 30.8%.
- the pigment used is silica with a particle size ranging from 1-10 microns.
- the total solids content of the coatable formulations ranged from 12.6% to 17.9%.
- US 4,460,637 describes an inkjet recording sheet having one or more layers; the top layer shows a large pore radius, while the overall layer or layers shows an additional pore radius which is much smaller.
- the dual pore radii can be obtained two ways. One is by forming two separate layers, in which the layer closest to the free surface contains pigment particles greater than 1 micron in diameter, while the bottom layer contains colloidal particles in the submicron range. The other method is by coating a single layer in which the pigment is formed by agglomerating colloidal particles before coating, or by choosing commercial pigments which are porous in nature. In either case, the pigment containing layer must be coated with a binder polymer such as polyvinyl alcohol in order to prevent the dusting which originates from cohesive failure of the coated layer.
- a binder polymer such as polyvinyl alcohol
- US 5,576,088 describes another two-layer ink receiving coating.
- the bottom layer (layer closest to the support material) comprises a pigment and binder.
- the binder is typically polyvinyl alcohol, and the pigment is a combination of large and colloidal inorganic particles. Because of the presence of the polymeric binder, the solids content of the base layer coating composition is 15%.
- the top layer also comprises pigment and a synthetic polymeric binder.
- the pigment may be a combination of large and colloidal particles (organic or inorganic), in which the content of colloidal-sized particles is chosen to be high enough, preferably 90 to 100 weight per cent, to impart a particular gloss.
- the binder content is kept low, so that coatings may be applied from higher solids melts; from 20-40%.
- the present invention discloses an inkjet recording medium comprising a substrate coated on at least one surface with a coating composition comprising a mixture of inorganic colloidal particles and non-colloidal pigments.
- an inkjet recording medium comprising a substrate coated on at least one surface with a coating composition comprising a mixture of inorganic colloidal particles and non-colloidal pigments.
- the present inkjet recording medium provides superior liquid absorption through a high level of porosity, resulting in fast ink drying and freedom from printed defects which originate from ink flooding and coalescence. Further, it completely eliminates the need for organic binders or fillers from the coating formulation used to produce the ink receiving layer, so that viscosity buildup is minimized and coatings may be acceptably deposited from very high solids melts. In this way, drying of the coated film requires less energy due to less required water removal. Furthermore, without polymeric binders porosity of the coating is enhanced. Such a composition provides fast drying of printed inks.
- the present invention provides a coating composition in which solids content is maximized and viscosity is minimized while providing a porous ink receiving layer demonstrating excellent ink drying characteristics, good image quality, and excellent resistance to ink smearing and bleeding in the presence of water or humidity.
- an efficient system which consists solely of particulate species, more particularly, a mixture of colloidal and non-colloidal particles.
- the inorganic colloidal particles provide rigidity and dusting-resistance to the layer without causing increased viscosity or reduced water resistance which polymeric binders cause.
- the larger particles which can be organic or inorganic in nature, provide ink absorption and porosity. Because of the higher solids content which is coatable in the absence of polymeric additives, curl and cockle during the coating and drying operation may be minimized.
- Suitable support materials include conventional paper, calendared paper, paper coated with extruded protective layers such as polyethylene, polypropylene or the like, and opaque or nonopaque polymeric films.
- polymeric film materials include polyethylene terephthalate, polyethylene naphthalate, poly-1,4-cyclohexane dimethylene terephthalate, polyvinyl chloride, polyimide, polycarbonate, polystyrene, cellulose acetate, or cellulose acetate propionate.
- the coating composition of the invention can be applied by any number of well-known techniques, such as dip-coating, rod-coating, blade coating, air knife coating, gravure coating and reverse roll coating, extrusion coating, slide coating, curtain coating, and the like. After coating, the layer is generally dried by simple evaporation, which may be accelerated by known techniques such as convection heating. Known coating and drying methods are described in further detail in Research Disclosure No. 308119, published Dec. 1989, pages 1007 to 1008.
- the coating composition can be coated either from water or organic solvents, however water is preferred for environmental reasons.
- the total solids content may range from 10% to 50% , but a preferred solids level is 40.
- the non-colloidal pigment may be any pigment commonly used in paper coatings, such as clay, calcium carbonate, titanium dioxide, calcined clay, aluminosilicates, amorphous silica and silicates, barium sulfate, satin white, or plastic pigments such as polystyrene or nylon beads.
- porous silica comprises the non-colloidal pigment, due to its wide availability, innocuous handling, and freedom from environmental concerns. While many types of amorphous and crystalline silica particles are manufactured by various methods and are commercially available, it might be preferred to use some porosity in order to accomplish faster ink drying in ink receiving layer. Synthetic amorphous silicas are preferred, as they have a very porous nature.
- Such materials can be successfully manufactured as either precipitated silica or silica gels. While their porosity is helpful in the absorption of ink, noncolloidal particles with extremely high levels of porosity are not as useful in the current invention as those with intermediate levels of porosity. This is because very porous silica particles absorb too much of the water used in the coating formulation, causing an unacceptable increase in viscosity, necessitating a decrease in solids level to obtain a coatable formulation. Porosity is commonly measured by oil absorption, in grams of oil per gram of silica. Preferred levels range from 50-350g/g, preferably 100-240 g/g.
- the colloidal particles are typically dispersed in water or solvent. They may include but are not limited to silica, aluminum-modified silica, alumina, tin oxide, antimonate, or (layered)coated oxides.
- the particle size is 1 nm to 1 micron, preferably 10 to 50 nm.
- the colloidal pigment may be chosen from the same set of ceramic materials listed above.
- the primary characteristic of the colloidal particles is that they are sufficiently small to exist in a dispersed state in a liquid (preferably water) and have sufficient interparticle attractive forces to hold together, but not flow, under typical coating and drying conditions. Colloidal materials are usually defined as having a size range from 1 nm to 1 micron (Solid/Liquid Dispersions, Th. F.
- a positively charged colloidal particle is preferred; for example alumina (DispalTM, Condea Vista Chemicals) or alumina-coated silica (LudoxTM CL, DuPont).
- coating aids 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 per cent 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 additional overcoat might be preferred for dot gain control, reduction in feathering or bleed, or for gloss enhancement.
- a layer should be a thin polymeric layer which may serve to control ink absorption rates.
- Many appropriate materials are well known in the art and may be applied by a variety of methods. The use of film-forming hydrophilic colloids as binders in ink receiving elements is well known.
- hydrophilic materials which form excellent ink-receptive layers for aqueous inks include but are not limited to polyvinyl alcohols and their derivatives, polyvinyl pyrrolidone, sulfonated or phosphated polyesters, cellulose ethers and their derivatives, poly(2-ethyl-2-oxazoline), gelatin, casein, zein, albumin, chitin, chitosan, dextran, pectin, collagen derivatives, collodian, agar-agar, arrowroot, guar, carrageenan, tragacanth, xanthan, rhamsan, sulfonated polystyrenes, acrylamides and their derivatives, polyalkylene oxides and the like.
- the dry coverage of such a layer may range from 0.1 micrometer to 10 micrometers, but preferably ranges from 0.5 micrometers to 5 micrometers, and even more preferably ranges from 0.5 to 1.0 micrometers.
- Coating compositions were made by slowly adding a conventional porous non-colloidal powder to a colloidal suspension of an oxide ceramic. The mixtures were stirred thoroughly until they were free of agglomerates or obviously oversized particulates. The composition was coated without further addition by the wound wire rod technique. The compositions were coated on bare, untreated bond-grade paper and were allowed to dry in a conventional lab oven at 70°C. The dried coatings were printed with blocks of solid colors (cyan, magenta, yellow, black, red, green and blue) with a Canon BJC 610 or Canon BJC 620 inkjet printer at 360 dpi, special coated paper setting.
- solid colors cyan, magenta, yellow, black, red, green and blue
- Example 1 Silica IJ35 Ludox TM CL 42 60/40 12
- Example 2 Silica IJ35 LudoxTM AM 42 60/40 12
- Example 3 Ludox TM SK 38 56/44 11
- Example 4 Ludox TM TMA 45 63/37 13
- Example 5 NalcoTM 1056 42 60/40 12
- Example 6 Nalco TM 1034A 45 63/37 13
- Example 7 NalcoTM 8676 25 40/60 6.4
- Example 8 Vista TM 23N4-20 33 50/50 9
- Example 9 Mica LVT-600 Ludox TM AM 42 60/40 12
- Example 10 Titania Ludox TM CL 42 60/40 12
- Example 11 Mizukasil Ludox TM CL 42 60/40 12
- Example 12 Nylon 12 Ludox TM CL 42 60/40 12
- Comparative Example 13 Silica IJ35 none 40 0/100
- Noncolloidal particles
- Examples 23-29 demonstrate preferred ratios of colloidal to noncolloidal particles.
- the coating compositions were mixed as described above.
- the colloidal particle was LudoxTM CL (DuPont Specialty Chemicals) and the noncolloidal particle was GasilTMIJ35 (Crosfield).
- the coating solvent was water.
- the compositions were bead coated on calendared raw photobase paper and dried at 55°C. Dry coverages ranged from 21 to 24 grains/meter 2.
- Printed quality was evaluated for coalescence on the Canon BJC 4200 inkjet printer using Photo Inks by evaluating a patch of solid cyan for nonuniformity.
- Dry time was evaluated by printing solid strips of color on a Hewlett Packard 850C inkjet printer at 80 per cent relative humidity. Immediately after printing, a sheet of bond paper was pressed against the printed image and a heavy smooth metal roller was passed over the combination. The sheets were separated. The dye offset to the bond paper (cyan, magenta, yellow, red, green and blue) was inspected to identify which color offset to the bond paper for the longest time after printing. In each case, this was the blue ink. The spot on the offset sheet at which no more blue ink was visible was measured with respect to the spot at which zero time had passed (point of heaviest offset) between printing and applying the bond paper. This length was converted to time.
- Dot size was measured by printing low density patches of cyan ink from a Hewlett Packard 690C inkjet printer using standard inks. Diameter was measured directly using an optical microscope at 290X magnification.
- Example 26 shows the effect of overcoating the coating of Example 26 with a polymeric layer designed to control (i.e. slow) the absorption of ink into the porous particulate layer.
- This layer was slide coated (simultaneously from another slot during bead coating) over the coating composition used to form Example 26.
- the composition of the overcoat was an 80/20 (weight) mixture of cationically modified hydroxyethyl cellulose (Quatrisoft LM200, Amerchol) and methyl cellulose (Methocel A4M, Dow Chemical) in water.
- the per cent solids of the overcoat was 1.75%.
- the coatings were dried as described for examples 23-29.
- a coating was made which was identical to Example 1, except that it was coated directly on polyethylene-coated paper.
- the polyethylene surface was treated with a corona discharge prior to applying the coating formulation in order to aid in welling and adhesion.
- the coating was continuous and did not powder or flake from the support material. This demonstrates the wide range of support materials which may be successfully coated with the current invention.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Ink Jet (AREA)
Abstract
An inkjet recording medium comprising a substrate coated on at
least one surface with a coating composition comprising a mixture of
inorganiccolloidal particles and non-colloidal pigments.
Description
- This invention relates to an ink receptive material comprising a support material containing at least one layer consisting essentailly of a mixture of inorganic particles; specifically a mixture of colloidal (< 1 micron) and noncolloidal inorganic particulates.
- Ink receptive materials for inkjet printing or other liquid marking processes typically employ layers comprising materials which are particularly receptive to the solvent or carrier making up the ink. For example, when inks are based primarily on water, as they are for most commercially available desk top inkjet printers, the ink receiving layer could be comprised of a hydrophilic material so that the capacity of the receiving layer to swell in the ink solvent allows the printed areas to become quickly apparently dry and also prevents flooding of the ink on the surface. Alternatively, the ink receiving layer could be comprised primarily of particulate materials so that the coated layer is highly porous and is therefore able to carry the ink away from the printed surface quickly. By "primarily particulate" material, it is meant that most (over 50%) of the volume of the image receptive layer comprises distinct particles, either never in solution or precipitated during the coating process. This alternative would also give the impression of fast drying and would limit any flooding of the surface in areas of high ink deposit.
- For surfaces in which high gloss is not required, the porous coating approach is preferred as it is inexpensive and easily applied by common coating methods such as gravure coating. The particles which make up such a porous coating can be polymeric or inorganic, and may have a hydrophilic character. Such particles, when used for paper coatings, are typically referred to as pigments. In order for a coating made from a particulate material to have sufficient cohesive strength to avoid crumbling or flaking from the support, polymeric binders are added to the coating formulation. They act like glue to help adhere the particles to each other and to the coated support. Typically, these polymers are solution polymers such as polyvinyl alcohol or casein; or latex polymers such as styrene-butadiene or acrylonitrile-styrene-butadiene. If a latex polymer is preferred over a solution polymer as a binder, typically more latex is necessary in order to obtain sufficient cohesive strength in the layer. A further addition to such a coating formulation or an additional overcoat is typically a crosslinker capable of cross linking the hydroxyl or carboxyl groups introduced by the polymeric binder. This cross linking provides additional water resistance to the coating. Still further, polymeric mordants are often added to such ink receiving layers in order to impart waterfastness to the printing inks.
- US 5,616,409 describes an inkjet recording medium comprising a paper of defined density and Stockigt sizing degree over which an ink receptive layer has been coated. The coated layers comprise 75% pigment, 20% binder and 5% cationic polymeric mordant. The pigment consists of porous synthetic amorphous silica powder with particle sizes over 1 micron, and the binder is either polyvinyl alcohol or silanol-modified vinyl alcohol
- EP Application 0 754 560 describes a color inkjet recording sheet which is coated from an aqueous formulation containing a water-soluble crosslinkable polymeric binder, an absorptive pigment, a zirconium crosslinking agent, and a cationically modified polymer. Binder examples include water soluble polymers such as polyvinyl alcohol, hydroxyethyl cellulose and rice starch. The binder concentration, as a percent of total pigment+binder content, ranges from 12.7% to 30.8%. The pigment used is silica with a particle size ranging from 1-10 microns. The total solids content of the coatable formulations ranged from 12.6% to 17.9%.
- US 4,460,637 describes an inkjet recording sheet having one or more layers; the top layer shows a large pore radius, while the overall layer or layers shows an additional pore radius which is much smaller. The dual pore radii can be obtained two ways. One is by forming two separate layers, in which the layer closest to the free surface contains pigment particles greater than 1 micron in diameter, while the bottom layer contains colloidal particles in the submicron range. The other method is by coating a single layer in which the pigment is formed by agglomerating colloidal particles before coating, or by choosing commercial pigments which are porous in nature. In either case, the pigment containing layer must be coated with a binder polymer such as polyvinyl alcohol in order to prevent the dusting which originates from cohesive failure of the coated layer.
- US 5,576,088 describes another two-layer ink receiving coating. The bottom layer (layer closest to the support material) comprises a pigment and binder. The binder is typically polyvinyl alcohol, and the pigment is a combination of large and colloidal inorganic particles. Because of the presence of the polymeric binder, the solids content of the base layer coating composition is 15%. The top layer also comprises pigment and a synthetic polymeric binder. The pigment may be a combination of large and colloidal particles (organic or inorganic), in which the content of colloidal-sized particles is chosen to be high enough, preferably 90 to 100 weight per cent, to impart a particular gloss. The binder content is kept low, so that coatings may be applied from higher solids melts; from 20-40%.
- It would be useful to have a coating formulation that is substantially free of organic material as this would allow a substantial increase in coating composition solids.
- The present invention discloses an inkjet recording medium comprising a substrate coated on at least one surface with a coating composition comprising a mixture of inorganic colloidal particles and non-colloidal pigments.
- In another aspect of the invention there is disclosed an inkjet recording medium comprising a substrate coated on at least one surface with a coating composition comprising a mixture of inorganic colloidal particles and non-colloidal pigments.
- The present inkjet recording medium provides superior liquid absorption through a high level of porosity, resulting in fast ink drying and freedom from printed defects which originate from ink flooding and coalescence. Further, it completely eliminates the need for organic binders or fillers from the coating formulation used to produce the ink receiving layer, so that viscosity buildup is minimized and coatings may be acceptably deposited from very high solids melts. In this way, drying of the coated film requires less energy due to less required water removal. Furthermore, without polymeric binders porosity of the coating is enhanced. Such a composition provides fast drying of printed inks. It also provides a low viscosity, high solids fraction coating formulation which provides superior latitude in coating and drying processes and reduced deformation of fibrous supports such as paper during the coating operation. Furthermore, elimination of an organic species in the instant coatings allows for higher temperature post processing operations such as high temperature calendaring without the risk of polymer degradation.
- The present invention provides a coating composition in which solids content is maximized and viscosity is minimized while providing a porous ink receiving layer demonstrating excellent ink drying characteristics, good image quality, and excellent resistance to ink smearing and bleeding in the presence of water or humidity.
- Surprisingly, it was found that an efficient system could be provided which consists solely of particulate species, more particularly, a mixture of colloidal and non-colloidal particles. The inorganic colloidal particles provide rigidity and dusting-resistance to the layer without causing increased viscosity or reduced water resistance which polymeric binders cause. The larger particles, which can be organic or inorganic in nature, provide ink absorption and porosity. Because of the higher solids content which is coatable in the absence of polymeric additives, curl and cockle during the coating and drying operation may be minimized.
- Suitable support materials include conventional paper, calendared paper, paper coated with extruded protective layers such as polyethylene, polypropylene or the like, and opaque or nonopaque polymeric films. Examples of such polymeric film materials include polyethylene terephthalate, polyethylene naphthalate, poly-1,4-cyclohexane dimethylene terephthalate, polyvinyl chloride, polyimide, polycarbonate, polystyrene, cellulose acetate, or cellulose acetate propionate.
- The coating composition of the invention can be applied by any number of well-known techniques, such as dip-coating, rod-coating, blade coating, air knife coating, gravure coating and reverse roll coating, extrusion coating, slide coating, curtain coating, and the like. After coating, the layer is generally dried by simple evaporation, which may be accelerated by known techniques such as convection heating. Known coating and drying methods are described in further detail in Research Disclosure No. 308119, published Dec. 1989, pages 1007 to 1008.
- The coating composition can be coated either from water or organic solvents, however water is preferred for environmental reasons. The total solids content may range from 10% to 50% , but a preferred solids level is 40.
- The non-colloidal pigment may be any pigment commonly used in paper coatings, such as clay, calcium carbonate, titanium dioxide, calcined clay, aluminosilicates, amorphous silica and silicates, barium sulfate, satin white, or plastic pigments such as polystyrene or nylon beads. Preferably, porous silica comprises the non-colloidal pigment, due to its wide availability, innocuous handling, and freedom from environmental concerns. While many types of amorphous and crystalline silica particles are manufactured by various methods and are commercially available, it might be preferred to use some porosity in order to accomplish faster ink drying in ink receiving layer. Synthetic amorphous silicas are preferred, as they have a very porous nature. Such materials can be successfully manufactured as either precipitated silica or silica gels. While their porosity is helpful in the absorption of ink, noncolloidal particles with extremely high levels of porosity are not as useful in the current invention as those with intermediate levels of porosity. This is because very porous silica particles absorb too much of the water used in the coating formulation, causing an unacceptable increase in viscosity, necessitating a decrease in solids level to obtain a coatable formulation. Porosity is commonly measured by oil absorption, in grams of oil per gram of silica. Preferred levels range from 50-350g/g, preferably 100-240 g/g.
- The colloidal particles are typically dispersed in water or solvent. They may include but are not limited to silica, aluminum-modified silica, alumina, tin oxide, antimonate, or (layered)coated oxides. The particle size is 1 nm to 1 micron, preferably 10 to 50 nm. The colloidal pigment may be chosen from the same set of ceramic materials listed above. The primary characteristic of the colloidal particles is that they are sufficiently small to exist in a dispersed state in a liquid (preferably water) and have sufficient interparticle attractive forces to hold together, but not flow, under typical coating and drying conditions. Colloidal materials are usually defined as having a size range from 1 nm to 1 micron (Solid/Liquid Dispersions, Th. F. Thadros, Ed., Academic Press, 1987, p.1). They may be spherical, ellipsoidal, acicular or fibrillar in shape. Surfaces may be treated or polymer grafted in order to enhance dispersability. While the surface charge of such particles may vary widely based on chemical composition, any type may be used. Preferably, the charge at the surface of the particle should be opposite that of the dyes in the marking inks, if dyes are used. In this way, mordanting of the dyes may be facilitated, resulting in good bleed resistance and waterfastness. For example, if dyes are anionic as for most commercial inkjet inks, a positively charged colloidal particle is preferred; for example alumina (Dispal™, Condea Vista Chemicals) or alumina-coated silica (Ludox™ CL, DuPont).
- 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 per cent 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.
- In one embodiment of the invention, it is optional to overcoat the dried composition described above with an additional layer. While not essential to the invention, the additional overcoat might be preferred for dot gain control, reduction in feathering or bleed, or for gloss enhancement. Typically such a layer should be a thin polymeric layer which may serve to control ink absorption rates. Many appropriate materials are well known in the art and may be applied by a variety of methods. The use of film-forming hydrophilic colloids as binders in ink receiving elements is well known. Examples of hydrophilic materials which form excellent ink-receptive layers for aqueous inks include but are not limited to polyvinyl alcohols and their derivatives, polyvinyl pyrrolidone, sulfonated or phosphated polyesters, cellulose ethers and their derivatives, poly(2-ethyl-2-oxazoline), gelatin, casein, zein, albumin, chitin, chitosan, dextran, pectin, collagen derivatives, collodian, agar-agar, arrowroot, guar, carrageenan, tragacanth, xanthan, rhamsan, sulfonated polystyrenes, acrylamides and their derivatives, polyalkylene oxides and the like. Combinations of such materials may also be used. The dry coverage of such a layer may range from 0.1 micrometer to 10 micrometers, but preferably ranges from 0.5 micrometers to 5 micrometers, and even more preferably ranges from 0.5 to 1.0 micrometers.
- Coating compositions were made by slowly adding a conventional porous non-colloidal powder to a colloidal suspension of an oxide ceramic. The mixtures were stirred thoroughly until they were free of agglomerates or obviously oversized particulates. The composition was coated without further addition by the wound wire rod technique. The compositions were coated on bare, untreated bond-grade paper and were allowed to dry in a conventional lab oven at 70°C. The dried coatings were printed with blocks of solid colors (cyan, magenta, yellow, black, red, green and blue) with a Canon BJC 610 or Canon BJC 620 inkjet printer at 360 dpi, special coated paper setting.
Example Noncolloidal powder Colloidal species % solids Ratio of colloidal/non colloidal Dry coverage g/m2 Example 1 Silica IJ35 LudoxTM CL 42 60/40 12 Example 2 Silica IJ35 Ludox™ AM 42 60/40 12 Example 3 " LudoxTM SK 38 56/44 11 Example 4 " LudoxTM TMA 45 63/37 13 Example 5 " Nalco™ 1056 42 60/40 12 Example 6 " NalcoTM 1034A 45 63/37 13 Example 7 " Nalco™ 8676 25 40/60 6.4 Example 8 " VistaTM 23N4-20 33 50/50 9 Example 9 Mica LVT-600 LudoxTM AM 42 60/40 12 Example 10 Titania LudoxTM CL 42 60/40 12 Example 11 Mizukasil LudoxTM CL 42 60/40 12 Example 12 Nylon 12 LudoxTM CL 42 60/40 12 Comparative Example 13 Silica IJ35 none 40 0/100 uncoatable (too viscous) Comparative Example 14 " " 20 0/100 8 Comparative Example 15 none LudoxTM CL 30 100/0 13 Comparative Example 16 " LudoxTM AM 30 100/0 13 Comparative Example 17 " LudoxTM SK 30 100/0 10 Comparative Example 18 " LudoxTM TMA 34 100/0 14 Comparative Example 19 " NalcoTM 1056 30 100/0 13 Comparative Example 20 " NalcoTM 1034A 34 100/0 14 Comparative Example 21 " NalcoTM 8676 10 100/0 3.6 Comparative Example 22 " VistaTM 23N4-20 20 100/0 7.7 -
- Silica IJ35 Gasil IJ35 noncolloidal porous silica, particle size 4.5 microns (Crosfield Company)
- Mica LVT-600: LVT-600 low viscosity talc, particle size 2.4 microns (Barretts Minerals, Inc.)
- Titania: Acicular titania FTL-300, (Ishihara Corporation USA) Dimensions: 5 microns length x 0.3 microns width
- Mizukasil: Mizukasil P-78D noncolloidal porous silica, particle size 7 microns (Mizusawa Fine Chemicals)
- Nylon 12: Orgasol ultrafine polyamide, particle size 4.7 microns (Elf Atochem ATO)
-
-
- Ludox CL:TM Alumina-coated colloidal silica, 12 nm (DuPont Specialty Chemicals)
- Ludox AM:™ Colloidal silica stabilized with sodium aluminate, 12 nm (DuPont)
- Ludox SK: Combination of deionized colloidal silica with water soluble polymer, 12 nm (DuPont)
- Ludox TMA: Deionized colloidal silica, 22 nm (DuPont)
- Nalco 1056: Aluminum modified colloidal silica, 20 nm (Nalco Chemical Company)
- Nalco 1034A:™ Colloidal silica 20 nm (Nalco Chemical Company)
- Nalco 8676:™ Colloidal alumina, 2 nm (Nalco Chemical Company)
- Vista 23N4-20:™ Dispal 23N4-20 alumina, 90 nm (Condea Vista Company)
-
- The coatings were evaluated for the following attributes:
- Bleed: (Measures the propensity of a printed area to spread beyond its intended or
specified boundaries)
- 1: No noticeable bleed between colors or into unprinted areas
- 2: Some bleed
- 3: Unacceptable (severe) bleed
- Coalescence: (Nonuniformity of solid printed areas. Inks may puddle when
absorption is uneven, resulting in local nonuniformites of optical density)
- 1: No noticeable coalescence
- 2: Slight coalescence
- 3: Severe coalescence
- Waterfastness:
- 1: Colors do not run when water is dripped on them
- 2: Colors run slightly
- 3: Colors run severely
-
- The coating compositions were mixed as described above. In each case, the colloidal particle was Ludox™ CL (DuPont Specialty Chemicals) and the noncolloidal particle was Gasil™IJ35 (Crosfield). The coating solvent was water. The compositions were bead coated on calendared raw photobase paper and dried at 55°C. Dry coverages ranged from 21 to 24 grains/meter 2.
- Printed quality was evaluated for coalescence on the Canon BJC 4200 inkjet printer using Photo Inks by evaluating a patch of solid cyan for nonuniformity.
- Dry time was evaluated by printing solid strips of color on a Hewlett Packard 850C inkjet printer at 80 per cent relative humidity. Immediately after printing, a sheet of bond paper was pressed against the printed image and a heavy smooth metal roller was passed over the combination. The sheets were separated. The dye offset to the bond paper (cyan, magenta, yellow, red, green and blue) was inspected to identify which color offset to the bond paper for the longest time after printing. In each case, this was the blue ink. The spot on the offset sheet at which no more blue ink was visible was measured with respect to the spot at which zero time had passed (point of heaviest offset) between printing and applying the bond paper. This length was converted to time.
- Dot size was measured by printing low density patches of cyan ink from a Hewlett Packard 690C inkjet printer using standard inks. Diameter was measured directly using an optical microscope at 290X magnification.
Example Colloidal/Non -colloidal particles Per cent solids in formulation Printed Quality: Coalescence in Cyan (Canon BJC 4200 Photo Inks) Time to dry HP 850 inks Dot size HP 690 Standard Inks Cyan 23 40/60 50 Could not coat (powdery) Not tested Not tested 24 50/50 45 Poor coated quality Not tested Not tested 25 60/40 42 poor coated quality Not tested Not tested 26 65/35 40 good instant 90 microns 27 70/30 38 good instant 100 microns 28 80/20 35 fair 52 seconds 130 microns 29 90/10 32 poor 1 min 23 seconds 130 microns - These examples show the balance between coatability, coating quality, dry time and dot gain which show the advantage of intermediate compositions of colloidal:noncolloidal particulate ratios.
- The following examples show the effect of overcoating the coating of Example 26 with a polymeric layer designed to control (i.e. slow) the absorption of ink into the porous particulate layer. This layer was slide coated (simultaneously from another slot during bead coating) over the coating composition used to form Example 26. The composition of the overcoat was an 80/20 (weight) mixture of cationically modified hydroxyethyl cellulose (Quatrisoft LM200, Amerchol) and methyl cellulose (Methocel A4M, Dow Chemical) in water. The per cent solids of the overcoat was 1.75%. The coatings were dried as described for examples 23-29.
Example Dry coverage of overcoat, g/m2 Bleed in Canon 4200 with Photo Inks Bleed in HP 690 with standard inks 26 0 severe excellent 30 0.27 poor excellent 31 0.54 fair excellent 32 0.81 good excellent 33 1.08 good excellent - This data clearly shows that depending upon the ink set tested, a thin absorption control overcoat may be preferred.
- A coating was made which was identical to Example 1, except that it was coated directly on polyethylene-coated paper. The polyethylene surface was treated with a corona discharge prior to applying the coating formulation in order to aid in welling and adhesion. The coating was continuous and did not powder or flake from the support material. This demonstrates the wide range of support materials which may be successfully coated with the current invention.
Example | Comments- /Quality | Printer Tested | Bleed | Coalescence | Waterfastness |
No coating on paper | Canon BJC-610 | 2 | 2 | 2 | |
1 | " | 1 | 1 | 1 | |
2 | " | 1 | 1 | 3 | |
3 | " | 1 | 1 | 3 | |
4 | " | 1 | 1 | 3 | |
5 | " | 1 | 2 | 2 | |
6 | " | 2 | 1 | 3 | |
7 | " | 1 | 1 | 2 | |
8 | " | 1 | 1 | 2 | |
9 | " | 3 | 3 | 2 | |
10 | Canon BJC-620 | 1 | 2 | 1 | |
11 | " | 1 | 1 | 1 | |
12 | " | 2 | 1 | 1 | |
Comparative Examples: | |||||
13 | Could not coat | ||||
14 | Could not print (coating powdered off) | ||||
15 | Some bronzing in blue | Canon BJC-610 | 2 | 2 | 1 |
16 | " | 1 | 3 | 3 | |
17 | " | 2 | 3 | 3 | |
18 | " | 2 | 1 | 3 | |
19 | Bronzing in blue | " | 2 | 2 | 2 |
20 | " | 2 | 1 | 3 | |
21 | Bronzing effect in blue | " | 2 | 2 | 3 |
22 | Bronzing effect in blue | " | 2 | 3 | 2 |
Claims (10)
- An inkjet recording medium comprising a substrate coated on at least one surface with a coating composition comprising a mixture of inorganic colloidal particles and non-colloidal pigments.
- An inkjet recording medium comprising a substrate having disposed on a surface thereof, a coating composition that is free of an organic species.
- The inkjet recording medium of claim 1, 2, or 3 wherein the coating composition has a solids content of 10-70 weight % of the coating composition.
- The inkjet recording medium of claim 1 or 2, wherein the noncolloidal pigment in the coating composition is selected from clay, calcium carbonate, titanium dioxide, calcined clay, aluminosilicates, amorphous silica and silicates, barium sulfate, satin white and plastic pigments porous silica.
- The inkjet recording medium of claim 6, wherein the noncolloidal pigment is porous silica.
- The inkjet recording medium of claim 1 or 2, wherein the noncolloidal pigment in the coating composition has an oil absorption capacity between 100-240 grams of oil per grams of silica.
- The inkjet recording medium of claim 1 or 2, wherein the colloidal particle in the coating composition is selected from silica, aluminum-modified silica, alumina, tin oxide, antimonate, and coated oxides.
- The inkjet recording medium of claim 1 or 2, wherein the colloidal particles in the coating composition has a particle size between 1nm and 1 micron.
- The inkjet recording medium of claim 1, 2, or 3, wherein the coating composition further comprises coating aids.
- The inkjet recording medium of claim 12 wherein the amount of coating aids is between 0.01 and 0.30 weight percent based on the total solution.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US127534 | 1993-09-28 | ||
US12753498A | 1998-07-31 | 1998-07-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0976571A1 true EP0976571A1 (en) | 2000-02-02 |
Family
ID=22430614
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP99202390A Withdrawn EP0976571A1 (en) | 1998-07-31 | 1999-07-20 | Porous inkjet recording elements |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0976571A1 (en) |
JP (1) | JP2000052638A (en) |
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2842540A1 (en) | 2002-07-18 | 2004-01-23 | Eastman Kodak Co | MATERIAL FOR INKJET PRINTING IMAGE FORMATION |
FR2842541A1 (en) | 2002-07-18 | 2004-01-23 | Eastman Kodak Co | MATERIAL FOR INKJET PRINTING IMAGE FORMATION |
US6861112B2 (en) | 2002-11-15 | 2005-03-01 | Cabot Corporation | Dispersion, coating composition, and recording medium containing silica mixture |
WO2005049329A1 (en) * | 2003-11-05 | 2005-06-02 | Eastman Kodak Company | Inkjet recording element |
WO2005049331A1 (en) * | 2003-11-05 | 2005-06-02 | Eastman Kodak Company | Inkjet recording element |
WO2005049330A1 (en) * | 2003-11-05 | 2005-06-02 | Eastman Kodak Company | Inkjet recording element |
WO2005049328A1 (en) * | 2003-11-05 | 2005-06-02 | Eastman Kodak Company | Inkjet recording element |
FR2864116A1 (en) | 2003-12-19 | 2005-06-24 | Eastman Kodak Co | Ink jet printing paper has an ink-receiving coating containing a water-soluble binder and a special aluminosilicate polymer obtained by hydrolysis of aluminum and silicon compounds with alkali in presence of silanol groups |
FR2869924A1 (en) | 2004-05-07 | 2005-11-11 | Eastman Kodak Co | MATERIAL FOR IMAGING INKJET PRINTING |
FR2872736A1 (en) | 2004-07-08 | 2006-01-13 | Eastman Kodak Co | MATERIAL FOR IMAGING INKJET PRINTING |
WO2006013025A1 (en) | 2004-08-05 | 2006-02-09 | Eastman Kodak Company | Method for treating an inkjet recording element |
EP1642742A2 (en) * | 2004-09-30 | 2006-04-05 | Asahi Glass Company Ltd. | Ink jet recording sheet for plate-making mask film and process for producing flexographic printing plate |
WO2006084621A1 (en) | 2005-02-09 | 2006-08-17 | Eastman Kodak Company | Material intended for forming images by inkjet printing |
WO2007080377A1 (en) | 2006-01-12 | 2007-07-19 | Imperial Chemical Industries Plc | Thermal transfer printing |
US7297365B2 (en) | 2000-12-28 | 2007-11-20 | Canon Kabushiki Kaisha | Recorded matter, method of producing recorded matter, method for improving image fastness, image fastness-improving agent, image fastness improving kit, dispenser, and applicator |
WO2009073070A1 (en) | 2007-12-04 | 2009-06-11 | W. R. Grace & Co.-Conn. | Abrasion resistant media |
US7767281B2 (en) | 2004-02-03 | 2010-08-03 | Eastman Kodak Company | Inkjet recording element |
US7858160B2 (en) | 2003-07-18 | 2010-12-28 | Eastman Kodak Company | Inkjet recording element |
US7914617B2 (en) * | 2002-11-27 | 2011-03-29 | Tapesh Yadav | Nano-engineered inks, methods for their manufacture and their applications |
US8075963B2 (en) | 2006-02-07 | 2011-12-13 | Eastman Kodak Company | Material for forming images by inkjet printing |
US8377522B2 (en) | 2006-12-21 | 2013-02-19 | Eastman Kodak Company | Use of organoclays in inkjet receiver layer to prevent the ozone fade of print |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0529308A1 (en) * | 1991-08-27 | 1993-03-03 | Nippon Paper Industries Co., Ltd. | Ink jet recording paper |
US5198410A (en) * | 1992-02-19 | 1993-03-30 | Eastman Kodak Company | Thermal dye transfer receiving element with backing layer |
US5252535A (en) * | 1992-12-23 | 1993-10-12 | Eastman Kodak Company | Thermal dye transfer receiving element with antistat backing layer |
WO1994027830A1 (en) * | 1993-05-20 | 1994-12-08 | Rexham Graphics Inc. | Receptor sheet using low glass transition coating |
EP0673779A1 (en) * | 1994-03-04 | 1995-09-27 | Mitsubishi Paper Mills, Ltd. | Tack sheet for ink jet recording |
EP0685344A2 (en) * | 1994-05-19 | 1995-12-06 | Mitsubishi Paper Mills, Ltd. | Ink jet recording sheet and process for its production |
JPH10195276A (en) * | 1997-01-10 | 1998-07-28 | Gantsu Kasei Kk | Ink jet ink printing sheet and aqueous composition of cationic copolymer therefor |
WO1999021703A1 (en) * | 1997-10-24 | 1999-05-06 | Rexam Graphics | Printing medium comprised of porous medium |
-
1999
- 1999-07-20 EP EP99202390A patent/EP0976571A1/en not_active Withdrawn
- 1999-07-30 JP JP11216929A patent/JP2000052638A/en active Pending
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0529308A1 (en) * | 1991-08-27 | 1993-03-03 | Nippon Paper Industries Co., Ltd. | Ink jet recording paper |
US5198410A (en) * | 1992-02-19 | 1993-03-30 | Eastman Kodak Company | Thermal dye transfer receiving element with backing layer |
US5252535A (en) * | 1992-12-23 | 1993-10-12 | Eastman Kodak Company | Thermal dye transfer receiving element with antistat backing layer |
WO1994027830A1 (en) * | 1993-05-20 | 1994-12-08 | Rexham Graphics Inc. | Receptor sheet using low glass transition coating |
EP0673779A1 (en) * | 1994-03-04 | 1995-09-27 | Mitsubishi Paper Mills, Ltd. | Tack sheet for ink jet recording |
EP0685344A2 (en) * | 1994-05-19 | 1995-12-06 | Mitsubishi Paper Mills, Ltd. | Ink jet recording sheet and process for its production |
US5576088A (en) * | 1994-05-19 | 1996-11-19 | Mitsubishi Paper Mills Limited | Ink jet recording sheet and process for its production |
JPH10195276A (en) * | 1997-01-10 | 1998-07-28 | Gantsu Kasei Kk | Ink jet ink printing sheet and aqueous composition of cationic copolymer therefor |
WO1999021703A1 (en) * | 1997-10-24 | 1999-05-06 | Rexam Graphics | Printing medium comprised of porous medium |
Non-Patent Citations (1)
Title |
---|
DATABASE WPI Section Ch Week 199840, Derwent World Patents Index; Class A14, AN 1998-462987, XP002121690 * |
Cited By (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7297365B2 (en) | 2000-12-28 | 2007-11-20 | Canon Kabushiki Kaisha | Recorded matter, method of producing recorded matter, method for improving image fastness, image fastness-improving agent, image fastness improving kit, dispenser, and applicator |
FR2842541A1 (en) | 2002-07-18 | 2004-01-23 | Eastman Kodak Co | MATERIAL FOR INKJET PRINTING IMAGE FORMATION |
FR2842540A1 (en) | 2002-07-18 | 2004-01-23 | Eastman Kodak Co | MATERIAL FOR INKJET PRINTING IMAGE FORMATION |
US6861112B2 (en) | 2002-11-15 | 2005-03-01 | Cabot Corporation | Dispersion, coating composition, and recording medium containing silica mixture |
US8263685B2 (en) | 2002-11-27 | 2012-09-11 | Ppg Industries Ohio, Inc. | Nano-engineered inks, methods for their manufacture and their applications |
US7914617B2 (en) * | 2002-11-27 | 2011-03-29 | Tapesh Yadav | Nano-engineered inks, methods for their manufacture and their applications |
US7858160B2 (en) | 2003-07-18 | 2010-12-28 | Eastman Kodak Company | Inkjet recording element |
WO2005049329A1 (en) * | 2003-11-05 | 2005-06-02 | Eastman Kodak Company | Inkjet recording element |
WO2005049328A1 (en) * | 2003-11-05 | 2005-06-02 | Eastman Kodak Company | Inkjet recording element |
WO2005049330A1 (en) * | 2003-11-05 | 2005-06-02 | Eastman Kodak Company | Inkjet recording element |
WO2005049331A1 (en) * | 2003-11-05 | 2005-06-02 | Eastman Kodak Company | Inkjet recording element |
WO2005058604A1 (en) | 2003-12-19 | 2005-06-30 | Eastman Kodak Company | Inkjet recording element |
FR2864116A1 (en) | 2003-12-19 | 2005-06-24 | Eastman Kodak Co | Ink jet printing paper has an ink-receiving coating containing a water-soluble binder and a special aluminosilicate polymer obtained by hydrolysis of aluminum and silicon compounds with alkali in presence of silanol groups |
US7632555B2 (en) | 2003-12-19 | 2009-12-15 | Eastman Kodak Company | Inkjet recording element |
US7767281B2 (en) | 2004-02-03 | 2010-08-03 | Eastman Kodak Company | Inkjet recording element |
FR2869924A1 (en) | 2004-05-07 | 2005-11-11 | Eastman Kodak Co | MATERIAL FOR IMAGING INKJET PRINTING |
WO2005108101A1 (en) | 2004-05-07 | 2005-11-17 | Eastman Kodak Company | Method for improving the ozone stability of an inkjet recording element |
FR2872736A1 (en) | 2004-07-08 | 2006-01-13 | Eastman Kodak Co | MATERIAL FOR IMAGING INKJET PRINTING |
US7604342B2 (en) | 2004-08-05 | 2009-10-20 | Eastman Kodak Company | Method for treating an inkjet recording element |
WO2006013025A1 (en) | 2004-08-05 | 2006-02-09 | Eastman Kodak Company | Method for treating an inkjet recording element |
EP1642742A2 (en) * | 2004-09-30 | 2006-04-05 | Asahi Glass Company Ltd. | Ink jet recording sheet for plate-making mask film and process for producing flexographic printing plate |
EP1642742A3 (en) * | 2004-09-30 | 2006-08-30 | Asahi Glass Company Ltd. | Ink jet recording sheet for plate-making mask film and process for producing flexographic printing plate |
WO2006084621A1 (en) | 2005-02-09 | 2006-08-17 | Eastman Kodak Company | Material intended for forming images by inkjet printing |
WO2007080377A1 (en) | 2006-01-12 | 2007-07-19 | Imperial Chemical Industries Plc | Thermal transfer printing |
US8557355B2 (en) | 2006-01-12 | 2013-10-15 | Akzo Nobel Coatings International B.V. | Thermal transfer printing |
US8075963B2 (en) | 2006-02-07 | 2011-12-13 | Eastman Kodak Company | Material for forming images by inkjet printing |
US8377522B2 (en) | 2006-12-21 | 2013-02-19 | Eastman Kodak Company | Use of organoclays in inkjet receiver layer to prevent the ozone fade of print |
WO2009073070A1 (en) | 2007-12-04 | 2009-06-11 | W. R. Grace & Co.-Conn. | Abrasion resistant media |
Also Published As
Publication number | Publication date |
---|---|
JP2000052638A (en) | 2000-02-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0976571A1 (en) | Porous inkjet recording elements | |
US5246774A (en) | Ink-jet medium and ink-jet recording method making use of it | |
JP2877740B2 (en) | Recording medium, image forming method using the same, and printed matter | |
EP1329330B1 (en) | Recording material for ink-jet | |
KR100523239B1 (en) | Ink jet recording material, process for producing the same and ink jet recording method using the same | |
EP0878322B1 (en) | Ink jet recording material and process for producing the same | |
US20060194005A1 (en) | Ink-jet recording material | |
US6713160B2 (en) | Ink jet recording material | |
US6447111B1 (en) | Ink jet printing method | |
US6645582B2 (en) | Ink jet recording element | |
EP1613482B1 (en) | Inkjet recording element comprising particles and polymers | |
EP1029703B1 (en) | Ink-jet recording material with improved light-resistance | |
WO2001005599A1 (en) | Image receiving element and method of manufacturing the element | |
US20030044583A1 (en) | Ink jet recording element | |
JP4149764B2 (en) | Inkjet recording element | |
US6443570B1 (en) | Ink jet printing method | |
US6692123B2 (en) | Ink jet printing method | |
JP2008260299A (en) | Inkjet recording element | |
EP1319516B1 (en) | Ink jet recording element and printing method | |
JP4149765B2 (en) | Inkjet recording element | |
EP1288009B1 (en) | Ink jet recording element and printing method | |
JP3990238B2 (en) | Inkjet recording element and printing method | |
JP3964686B2 (en) | Inkjet recording element | |
JP3761920B2 (en) | Recording medium | |
US6632490B2 (en) | Ink jet recording element |
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: A1 Designated state(s): DE FR GB |
|
AX | Request for extension of the european patent |
Free format text: AL;LT;LV;MK;RO;SI |
|
17P | Request for examination filed |
Effective date: 20000708 |
|
AKX | Designation fees paid |
Free format text: DE FR GB |
|
17Q | First examination report despatched |
Effective date: 20011109 |
|
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: 20020320 |