WO1996018496A1 - Aqueous ink receptive ink jet receiving medium yielding a water resistant ink jet print - Google Patents

Aqueous ink receptive ink jet receiving medium yielding a water resistant ink jet print Download PDF

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Publication number
WO1996018496A1
WO1996018496A1 PCT/US1995/016371 US9516371W WO9618496A1 WO 1996018496 A1 WO1996018496 A1 WO 1996018496A1 US 9516371 W US9516371 W US 9516371W WO 9618496 A1 WO9618496 A1 WO 9618496A1
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WO
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Prior art keywords
ink jet
receiving medium
random copolymer
ink
copolymer
Prior art date
Application number
PCT/US1995/016371
Other languages
French (fr)
Inventor
Brian L. Anderson
Original Assignee
Rexam Graphics Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rexam Graphics Inc. filed Critical Rexam Graphics Inc.
Priority to DE69519392T priority Critical patent/DE69519392T2/en
Priority to AT95944618T priority patent/ATE197425T1/en
Priority to EP95944618A priority patent/EP0801602B1/en
Priority to JP51928196A priority patent/JP2001520591A/en
Priority to AU47393/96A priority patent/AU4739396A/en
Publication of WO1996018496A1 publication Critical patent/WO1996018496A1/en

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5254Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5245Macromolecular coatings characterised by the use of polymers containing cationic or anionic groups, e.g. mordants

Definitions

  • the present invention relates to an ink jet receiving medium.
  • the present invention relates to an ink jet receiving medium v ich yields a water resistant ink jet print and a process for providing such a water resistant ink jet print.
  • Ink jet systems are typically comprised of three components: the printer, the ink and the receptor.
  • the printer controls the size, number and placement of the ink droplets and contains the transport system.
  • the ink provides the colorants which form the image, and the receptor provides the medium which accepts and holds the ink.
  • the quality and stability of the resultant ink jet print is a function of the system as a whole. However, the composition and interaction of the ink and the receptor material most affect the quality and stability of the imaged product.
  • the ink be absorbed as rapidly as possible, and that the spread of ink droplets be adequate.
  • the resultant image should be excellent in storability, durability and water resistance.
  • Ink compositions which are useful in ink jet recording systems are well known and generally contain water, organic solvents and dyes.
  • European Patent 0,294,155 discloses an ink jet composition useful in ink jet recording consisting of a water based vehicle containing about 30-99% wt. water with the balance made up of high boiling solvents such as glycol, glycol ethers, pyrrolidones and amides.
  • the inks contain preferably acid or direct dyes.
  • a polyhydric alcohol is added for the prevention of the clogging of nozzles and improvement of ejection stability.
  • ink jet systems fall broadly into two categories; those that employ high organic solvent-water based inks, and those that are essentially aqueous.
  • Aqueous inks normally contain up to 10% of a high boiling solvent such as diethylene glycol, whereas high organic solvent inks contain, in addition to water, about 50% of a high boiling organic solvent such as diethylene glycol.
  • the resultant ink jet print using either of these types of ink has poor water resistance (i.e., the dye image leaches out or the image layer containing the dye dissolves when contacted with water) . Additionally, the dye image is prone to smudging.
  • Ink jet film compositions are normally sensitive to water and the print can dissolve and leach out. Also, under humid conditions, the print can bleed thereby losing definition. This deterioration is accentuated when the inks employ high boiling solvents, such as glycols. Conventional ink jet prints often lack light resistance and good file aging properties as well. A solution to all the above shortcomings is required to achieve acceptable print stability.
  • Polymeric films for use as recording media represent a special problem in ink jet recording because their surfaces are hydrophobic or quasi-hydrophobic. Even when their surfaces are treated with special coatings to accept and absorb the inks, it is difficult to obtain the requisite qualities of image density and resolution without incurring tack, smear, image bleed, water solubilization of the ink receptive matrix, or other undesirable properties.
  • U.S. Patent No. 4,503,111 assigned to Tektronics discloses a recording medium having a non- porous ink-receiving layer formed by using primarily a polyvinylpyrrolidone.
  • a recording medium has various problems. These problems include a recorded image low in light fastness, or that due to the stickiness of the surface of the inked receiving layer, blocking is liable to occur when the printed media are placed upon one another, or when paper is superposed on the recorded surface.
  • films useful in ink jet printing which films comprise a transparent, translucent or opaque substrate, having on at least one side thereof a water- insoluble, water-absorptive and ink-receptive matrix comprised of a hydrogel complex and a polymeric high molecular weight quaternary ammonium salt.
  • U.S. Patent No. 4,877,680 to Sakaki et al. relates to a recording medium comprising a substrate and a non- porous ink receiving layer.
  • the ink receiving layer contains a water-insoluble polymer containing a cationic resin.
  • the recording medium may be employed for recording by attaching droplets of a recording liquid thereon.
  • U.S. Patent No. 4,576,867 to Miyamoto relates to an ink jet recording paper wherein by attaching a cationic resin having a structure represented by the following general formula (I) to at least the surface of an ink jet recording paper, the water-resistance and the sunlight fastness of the image formed on the ink jet recording paper can be improved:
  • R,, R 2 and R 3 represent alkyl group; m represents a number from 1 to 7; n represents a number from 2 to 20; and Y represents an acid residue.
  • European patent publication 0,500,021 Al relates to a recording method and recording film comprising a transparent substrate, a porous alumina hydrate layer formed on the substrate and an opaque porous layer laminated on the alumina hydrate layer.
  • Ink jet prints have always been prone to UV light fade, and moisture sensitivity. Since the majority of the ink jet inks currently used in desktop and graphic arts applications are composed mainly of water, the ink jet receiver coatings need to be water receptive. The challenge is to develop a hydrophilic, aqueous ink receptive coating that yields a water resistant ink jet print.
  • an object of the present invention is to provide a novel recording medium for ink jet recording which is particularly excellent in ink receptivity, sharpness and water resistance.
  • Another object of the present invention is to provide a recording medium for ink jet recording which is excellent in water resistance, even under highly humid conditions, and also free from migration or leaching of the print ink when water droplets contact the surface of the recorded image, or when left to stand under highly humid conditions.
  • Still another object of the present invention is to provide a water resistant ink jet print and method thereof.
  • a receiving medium comprising a substrate and an ink receiving layer provided thereon, said ink receiving layer comprising a random copolymer of a vinyl amide and acrylic acid or methacrylic acid or their esters, a cationic resin and a crosslinking agent.
  • the random copolymer is a copolymer of vinylpyrrolidone and acrylic acid or acrylamide and acrylic acid.
  • a recording medium comprising a substrate and an ink receiving layer provided thereon, said ink receiving layer comprising a 75% vinyl pyrrolidone/ 25% acrylic acid random copolymer, 10% by weight of a cationic resin and 3 to 4% by weight of a crosslinking agent based on the copolymer.
  • the copolymer is an acryla ide/acrylic acid random copolymer.
  • a process for providing a water resistant ink jet print by attaching droplets of a recording liquid on a recording medium, said recording liquid containing a water-soluble dye, water and an organic solvent, said recording medium comprising an ink receiving layer provided on a substrate, with the ink receiving layer comprising a crosslinked vinyl amide acrylic acid or methacrylic acid or ester thereof random copolymer and, a cationic resin.
  • the present invention relates to an ink jet recording medium.
  • the ink jet recording medium of the present invention comprises a receiving layer which is water resistant and includes a vinyl amide/acrylic acid or methacrylic acid or esters thereof random copolymer, a cationic resin and a crosslinking agent.
  • the ink receiving layer is generally coated on a suitable substrate and dried to effect crosslinking of the copolymer.
  • suitable vinyl amide/acrylic acid or methacrylic acid or esters thereof random copolymer ⁇ when properly crosslinked, form the backbone of a water resistant ink jet coating.
  • This coating can be applied to, but is not limited to, the following substrates: a clear film, a polyethylene clad paper (photobase), adhesive backed vinyl, paper and canvas.
  • the vinyl amide monomer used in preparing the random copolymer can be derived from either an N-vinyl amide or a vinyl amide such as acrylamide.
  • the most preferred N-vinyl amide is vinyl pyrrolidone.
  • Acrylamide is another preferred monomer for use in preparing the random copolymer used in the present invention.
  • the monomer copolymerized with the vinyl amide is an acrylic acid or methacrylic acid, or an ester of acrylic acid or methacrylic acid.
  • the more preferred acrylates and methacrylates are the methylacrylate, ethylacrylate and methylmethacrylate esters.
  • acrylic acid be copolymerized with either vinyl pyrrolidone or acrylamide for purposes of the present invention, as these two copolymers have been found to be most easily available and most useful.
  • International Specialty Products of Wayne, New Jersey manufactures a line of suitable vinyl pyrrolidone/acrylic acid random copolymer products under the trade name Acrylidones. The following table summarizes various characteristics of commercially available vinyl pyrrolidone/acrylic acid random copolymers.
  • a preferred resin for overall imaging properties contains 75% vinyl pyrrolidone (for example, see ACP- 1001 and ACP-1033 above) .
  • the ink receptivity decreases, generally resulting in poor print quality and long ink dry times. More specifically, it has been found that grades containing 75% vinyl pyrrolidone work the best for print quality and ink dry time, while grades containing 50% vinyl pyrrolidone and 50% acrylic acid are marginal, and grades containing 25% vinyl pyrrolidone and 75% acrylic acid do not receive ink at all.
  • the preferred acrylamide/acrylic acid copolymers are also commercially available. Suitable copolymers can be obtained, for example, from Cytec Industries Inc. of West Patterson, N.J. under the trademark CYANAMER. Conventional crosslinking agents are suitable for use in the present invention. However, the aziridine class of polyfunctional crosslinkers is most preferred for the purposes of the present invention. Suitable aziridine crosslinkers are commercially available, for example, such as crosslinkers CX-100 available from Zeneca Resins of Wilmington, Mass.; XAMA-7 and XAMA-2, both available from Cordova Chemical Co. of North Muskegeon, Michigan. Such polyfunctional crosslinkers generally have a functionality greater than 2, and more preferably in the range of from 2.5 to 3.5.
  • the amount of crosslinking agent present is an amount sufficient to crosslink the copolymer so as to achieve a water resistance that allows the print to be immersed in water while still maintaining the integrity of the coating, and hence the print. It was determined empirically that from about 3 to about 13% of an aziridine crosslinker, based on the weight of random copolymer, is a preferable amount in terms of print quality and water resistance. More preferably is an amount of from 3 to 5 wt. %, and most preferably from 3 to about 4 wt. %. If too little crosslinker is used, the coatings can be very tacky and not water resistant at all. If too much crosslinker is used, the coating is generally not very receptive to the aqueous inks, and the resulting prints are poor, with much ink pooling and long ink dry times.
  • the crosslinking of the random copolymer is preferably accomplished during the drying step, for purposes of convenience. It may also be accomplished in a separate step, if preferred.
  • the crosslinked copolymers work well as a good water resistant backbone for the coating, they are preferably used in combination with a cationic substance.
  • a cationic substance is required to "lock" the dyes in the coating matrix.
  • Conventional cationic resins are suitable for use in the coating of the present invention.
  • Quaternary ammonium compounds are preferable, of these, the higher molecular weight compounds are most preferable and provide the best overall print quality and water resistance properties.
  • CPS Chemical Company of Old Bridge, New Jersey manufactures several lines of cationic polymers by the trade name of Agefloc, which are suitable for use in the present invention. Of these, a high molecular weight poly (hydroxyalkene dimethyl ammonium chloride) called Agefloc A-50HV is most preferable with respect to the overall results for print quality and water resistance.
  • Other high molecular weight cationic resins include the Agefloc A- 50 and A-40HV.
  • the amount of cationic material used is generally an amount sufficient to preclude bleeding of the ink when the print is immersed in water, i.e., an ink migration precluding amount. It was empirically determined that preferred print quality and water resistance results are obtained with the use of a formulation containing about 5 to about 10% of the quaternary ammonium resin, as based on the % solids (wt.) of the random copolymer resin. If too little of the quaternary resin is used, the print quality is poor, and the dye runs when immersed in water. If too much of the quaternary resin is used, the initial print quality is poor, and the coatings are tacky.
  • the receiving layer of the present invention can be coated onto a substrate using any conventional coating process.
  • the coating must generally be dried sufficiently to assure proper crosslinking.
  • the present invention also includes a process for providing a water resistant ink jet print. The process includes coating a suitable substrate with a vinyl amide acrylic acid or methacrylic acid or ester thereof random copolymer, a cationic resin and a crosslinking agent; curing the coating; and applying droplets of a recording liquid on the coating.
  • the above mix was prepared by mixing the Syloid 620 and water on a magnetic stirring plate for 1 minute.
  • the Acrylidone and ammonium hydroxide were added and the mixture was stirred on the magnetic stirrer for an additional minute.
  • the final three ingredients (2- pyrrolidone, Agefloc A-50HV, Xama 7) were added, and the mixture was stirred for a final five minutes on a magnetic stirring plate.
  • the composition was then coated onto 380 gauge Melinex 534 with a gapped number 70 Mayer rod to achieve a coating thickness of about 0.40 mils.
  • the coating was dried in a laboratory Blue M convection oven for 5 minutes at 260° F. This drying step also resulted in the crosslinking of the Acrylidone copolymer.
  • the sample was then printed on a Canon BJC600 ink jet printer using a full color block test pattern. Visual densities of cyan, magenta, yellow, black, red, green and blue were run using an XRITE 938 color densitometer. The print was allowed to air dry for 1 hour, then it was completely immersed in water for 10 minutes. The visual densities were repeated after the immersion, and calculations were performed to get the % retained density. The results are summarized in Table 2 below.
  • Example 3 uses two mixes.
  • the first mix (Mix A) was prepared with the same composition as that in Example 1 and applied to the substrate in the same manner as in Example 1.
  • the second mix (Mix B) was prepared in the following manner:
  • Gohsenal N-300 and PVP K90 solutions were blended and mixed for 30 seconds on a magnetic stir plate.
  • the Zonyl FSJ and water were added, and stirred for 5 minutes on a magnetic stir plate.
  • Mix B was then applied as a topcoat onto the coating of that previously prepared according to Example 1 with a wire wound number 10 Mayer rod.
  • the sample was then dried at 240° F in a Blue M convection oven for 2 minutes.
  • Example 2 The above mixture was prepared in the same manner as described in Example 1.
  • the coating, printing, and water immersion were performed in the same manner as in Example 1. The results are summarized in Table 2 below.
  • Amorphous silica is available from W.R. Grace, Baltimore, MD as Syloid 620.
  • Vinylpyrrolidone/acrylic acid copolymer is available from International Specialty Polymers of Wayne, NJ as Acrylidone ACP-1001.
  • Aziridine crosslinker is available from Cordova Chemical of North Muskegeon, MI as Xama 7.
  • Prebonded white polyester is available from ICI Films of Hopewell, VA as Melinex 534.
  • Examples 1 and 2 both had very good print quality and excellent water resistance properties.
  • a small amount of a fully hydrolyzed polyvinyl alcohol is added, as in Example 2, the print tack is reduced significantly.
  • the print tack can be reduced even further, and the colors can be made very glossy, by adding a thin PVP/fully hydrolyzed polyvinyl alcohol topcoat as seen in Example 3.
  • additional resins such as polyvinyl alcohol or an acrylic resin
  • Example 1 the resulting coating is very tacky, and is easily dissolved in water.
  • Comparative Example 2 the print quality is poor indicating a high amount of bleed and ink pooling.
  • the combination of the random copolymer together with the crosslinker and the cationic resin is important.
  • the above mixture was prepared by mixing the Syloid
  • the Cyanamer was slowly added, and stirred for 15 minutes.
  • the ammonium hydroxide was added and the mixture was stirred for a final fifteen minutes on a magnetic stirring plate.
  • the composition was then coated onto 380 gauge Melinex 534 with a gapped number 70 Mayer rod to achieve a coating thickness of about 0.40 mils.
  • the coating was dried in a laboratory Blue M convection oven for 5 minutes at 260 F.
  • the samples were then printed on a Canon BJC600e ink jet printer, and an Encad NovaJet ink jet printer using a full color block test pattern.
  • the print was allowed to air dry for 1 hour, then it was completely immersed in water for 10 minutes.
  • the print quality, evaluated as in Example 1, water immersion and wet rub resistance were all very good.
  • the reagents used in the foregoing Example are commercially available and may be generally described as follows:
  • Syloid 620 amorphous silica from W.R. Grace, Baltimore, Md.
  • CX-100 aziridine cross linker from Zeneca Resins of Wilmington, Ma. Agefloc A-50HV — poly(Hydroxyalkene ammonium chloride) from C.P.S. Chemicals of Old Bridge, N.J.
  • Fluorad FC-135 cationic fluorosurfactant from 3M of St. Paul, Minnesota
  • Gafquat 755N quaternized copolymer of vinylpyrrolidone and dimethylaminoethyl methacrylate from International Specialty Products of Wayne, N.J.
  • Melinex 534 prebonded white polyester from ICI Films of Hopewell, Va.

Abstract

An aqueous ink jet receiving medium which yields a water resistant ink jet print and a process for providing a water resistant ink jet print are disclosed. The water resistant ink jet receiving medium comprises an ink receptive layer of a crosslinked vinyl amide acrylic acid or methacrylic acid or ester thereof random copolymer and a cationic resin. The random copolymer employed is preferably a vinyl pyrrolidone/acrylic acid or acrylamide/acrylic acid copolymer.

Description

AQUEOUS INK RECEPTIVE INK JET RECEIVING MEDIUM YIELDING A WATER RESISTANT INK JET PRINT
Field of the Invention
The present invention relates to an ink jet receiving medium. In particular, the present invention relates to an ink jet receiving medium v ich yields a water resistant ink jet print and a process for providing such a water resistant ink jet print.
Description of Related Art Printers using sprayable inks, such as ink jet printers, have become more popular in recent years due to a number of desirable features. Specifically, these systems operate quietly at high speed without the need for external developing or fixation procedures. Moreover, through the use of multiple ink jet heads various colors may be obtained which are suitable for a variety of applications. These printers typically employ ink jet heads having small orifices that propel ink droplets and are used in various electronic printing applications. Various methods for ejecting droplets of ink have been developed. These methods include the use of an electrostatic attraction system, the use of a piezoelectric element to impart mechanical vibration or displacement to the ink, and pressurizing the ink by heating. Thus, it is no wonder that such a recording method which generates less noise and is capable of performing high-speed printing and multi-color printing is in great demand.
Ink jet systems are typically comprised of three components: the printer, the ink and the receptor. The printer controls the size, number and placement of the ink droplets and contains the transport system. The ink provides the colorants which form the image, and the receptor provides the medium which accepts and holds the ink. The quality and stability of the resultant ink jet print is a function of the system as a whole. However, the composition and interaction of the ink and the receptor material most affect the quality and stability of the imaged product.
More specifically, it is desired that the ink be absorbed as rapidly as possible, and that the spread of ink droplets be adequate. The resultant image should be excellent in storability, durability and water resistance.
Ink compositions which are useful in ink jet recording systems are well known and generally contain water, organic solvents and dyes. European Patent 0,294,155 discloses an ink jet composition useful in ink jet recording consisting of a water based vehicle containing about 30-99% wt. water with the balance made up of high boiling solvents such as glycol, glycol ethers, pyrrolidones and amides. The inks contain preferably acid or direct dyes. Optionally, a polyhydric alcohol is added for the prevention of the clogging of nozzles and improvement of ejection stability.
Typically, ink jet systems fall broadly into two categories; those that employ high organic solvent-water based inks, and those that are essentially aqueous. Aqueous inks normally contain up to 10% of a high boiling solvent such as diethylene glycol, whereas high organic solvent inks contain, in addition to water, about 50% of a high boiling organic solvent such as diethylene glycol. The resultant ink jet print using either of these types of ink has poor water resistance (i.e., the dye image leaches out or the image layer containing the dye dissolves when contacted with water) . Additionally, the dye image is prone to smudging.
Ink jet film compositions are normally sensitive to water and the print can dissolve and leach out. Also, under humid conditions, the print can bleed thereby losing definition. This deterioration is accentuated when the inks employ high boiling solvents, such as glycols. Conventional ink jet prints often lack light resistance and good file aging properties as well. A solution to all the above shortcomings is required to achieve acceptable print stability.
Polymeric films for use as recording media represent a special problem in ink jet recording because their surfaces are hydrophobic or quasi-hydrophobic. Even when their surfaces are treated with special coatings to accept and absorb the inks, it is difficult to obtain the requisite qualities of image density and resolution without incurring tack, smear, image bleed, water solubilization of the ink receptive matrix, or other undesirable properties.
The use of water/glycol ink systems presents a special problem. At high humidities, a phenomenon described as image bleed, occurs. The ink jet printer applies small ink droplets in a selective pattern to form the images. These droplets are absorbed into the coating on the film surface to form dots. After initial absorption, the dye continues to spread laterally. Some post imaging spread is desirable to fill in the white areas between the dots and obtain good image density. At high humidities, however, this spreading continues and causes the image to spread excessively, that is, to bleed thereby losing image sharpness or resolution. Ink vehicles which do not contain high boiling solvents such as glycol do not exhibit this level of image bleed. Various attempts have been made to solve these problems in an effort to provide the optimal receptor. Approaches to the problem of hydrophobic surfaces include the use of polymers alone or in admixture as ink receptive coatings; see for example, U.S. Patent Nos. 4,503,111; 3,889,270; 4,564,560; 4,555,437 and 4,578,285. Multiple coatings have also been employed in trying to overcome the various problems associated with the hydrophobic nature of recording media; illustrative of these coatings are those described in U.S. Patent No. 4,379,804, Japanese Patent Number 01041589 and Japanese Disclosure Numbers 86-132377; 86-074879 and 86-41549. Additionally, the use of mordants to help fix the dye and minimize bleed has been the subject of a number of patents, including U.S. Patent Nos. 4,554,181; 4,578,285 and 4,547,405.
Moreover, there is a strong demand for a recording medium having light transmissivity and a recording medium having gloss on the surface. In these cases it is essential that the surface of the recording medium be non-porous. In this regard, in order to enhance ink affinity and ink receptivity, it has been the practice in the prior art to use a recording medium comprising a non-porous ink-receiving layer formed by use of a water- soluble polymer.
For example, U.S. Patent No. 4,503,111 assigned to Tektronics discloses a recording medium having a non- porous ink-receiving layer formed by using primarily a polyvinylpyrrolidone. However, such a recording medium has various problems. These problems include a recorded image low in light fastness, or that due to the stickiness of the surface of the inked receiving layer, blocking is liable to occur when the printed media are placed upon one another, or when paper is superposed on the recorded surface. U.S. Patent No. 5,206,071 to Atherton et al. relates to film mediums useful in ink jet printing which films comprise a transparent, translucent or opaque substrate, having on at least one side thereof a water- insoluble, water-absorptive and ink-receptive matrix comprised of a hydrogel complex and a polymeric high molecular weight quaternary ammonium salt.
U.S. Patent No. 4,877,680 to Sakaki et al. relates to a recording medium comprising a substrate and a non- porous ink receiving layer. The ink receiving layer contains a water-insoluble polymer containing a cationic resin. The recording medium may be employed for recording by attaching droplets of a recording liquid thereon. U.S. Patent No. 4,576,867 to Miyamoto relates to an ink jet recording paper wherein by attaching a cationic resin having a structure represented by the following general formula (I) to at least the surface of an ink jet recording paper, the water-resistance and the sunlight fastness of the image formed on the ink jet recording paper can be improved:
(I)
Figure imgf000007_0001
wherein R,, R2 and R3 represent alkyl group; m represents a number from 1 to 7; n represents a number from 2 to 20; and Y represents an acid residue.
European patent publication 0,500,021 Al relates to a recording method and recording film comprising a transparent substrate, a porous alumina hydrate layer formed on the substrate and an opaque porous layer laminated on the alumina hydrate layer.
One of the major drawbacks of an ink jet print has always been the lack of long term durability of the images. Ink jet prints have always been prone to UV light fade, and moisture sensitivity. Since the majority of the ink jet inks currently used in desktop and graphic arts applications are composed mainly of water, the ink jet receiver coatings need to be water receptive. The challenge is to develop a hydrophilic, aqueous ink receptive coating that yields a water resistant ink jet print.
Accordingly, an object of the present invention is to provide a novel recording medium for ink jet recording which is particularly excellent in ink receptivity, sharpness and water resistance.
Another object of the present invention is to provide a recording medium for ink jet recording which is excellent in water resistance, even under highly humid conditions, and also free from migration or leaching of the print ink when water droplets contact the surface of the recorded image, or when left to stand under highly humid conditions.
Still another object of the present invention is to provide a water resistant ink jet print and method thereof.
These and other objects of the present invention will become apparent upon a review of the specification and the claims appended thereto.
SUMMARY OF THE INVENTION
According to one aspect of the present invention, there is provided a receiving medium comprising a substrate and an ink receiving layer provided thereon, said ink receiving layer comprising a random copolymer of a vinyl amide and acrylic acid or methacrylic acid or their esters, a cationic resin and a crosslinking agent. Preferably, the random copolymer is a copolymer of vinylpyrrolidone and acrylic acid or acrylamide and acrylic acid. Upon drying the ink receiving layer subsequent to coating onto the substrate, the random copolymer is preferably crosslinked.
According to another aspect of the present invention, there is provided a recording medium comprising a substrate and an ink receiving layer provided thereon, said ink receiving layer comprising a 75% vinyl pyrrolidone/ 25% acrylic acid random copolymer, 10% by weight of a cationic resin and 3 to 4% by weight of a crosslinking agent based on the copolymer. In another aspect, there is provided such a recording medium where the copolymer is an acryla ide/acrylic acid random copolymer.
According to a further aspect of the present invention, there is provided a process for providing a water resistant ink jet print by attaching droplets of a recording liquid on a recording medium, said recording liquid containing a water-soluble dye, water and an organic solvent, said recording medium comprising an ink receiving layer provided on a substrate, with the ink receiving layer comprising a crosslinked vinyl amide acrylic acid or methacrylic acid or ester thereof random copolymer and, a cationic resin.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS The present invention relates to an ink jet recording medium. The ink jet recording medium of the present invention comprises a receiving layer which is water resistant and includes a vinyl amide/acrylic acid or methacrylic acid or esters thereof random copolymer, a cationic resin and a crosslinking agent. The ink receiving layer is generally coated on a suitable substrate and dried to effect crosslinking of the copolymer. Applicants have found experimentally that suitable vinyl amide/acrylic acid or methacrylic acid or esters thereof random copolymerε, when properly crosslinked, form the backbone of a water resistant ink jet coating. This coating can be applied to, but is not limited to, the following substrates: a clear film, a polyethylene clad paper (photobase), adhesive backed vinyl, paper and canvas.
The vinyl amide monomer used in preparing the random copolymer can be derived from either an N-vinyl amide or a vinyl amide such as acrylamide. The most preferred N-vinyl amide is vinyl pyrrolidone. Acrylamide is another preferred monomer for use in preparing the random copolymer used in the present invention. The monomer copolymerized with the vinyl amide is an acrylic acid or methacrylic acid, or an ester of acrylic acid or methacrylic acid. Among the more preferred acrylates and methacrylates are the methylacrylate, ethylacrylate and methylmethacrylate esters. It is most preferred, however, that acrylic acid be copolymerized with either vinyl pyrrolidone or acrylamide for purposes of the present invention, as these two copolymers have been found to be most easily available and most useful. International Specialty Products of Wayne, New Jersey manufactures a line of suitable vinyl pyrrolidone/acrylic acid random copolymer products under the trade name Acrylidones. The following table summarizes various characteristics of commercially available vinyl pyrrolidone/acrylic acid random copolymers.
TABLE 1
VP/AA RATIO MOLECULAR ACID NUMBER WEIGHT
ACP-1001 75:25 250,000 170-210
ACP-1004 50:50 250,000 365-405
ACP-1005 25:75 250,000 560-600
ACP-1033 75:25 80,000 170-210
ACP-1041 50:50 80,000 365-405
ACP-1042 25:75 80,000 560-600 A preferred resin for overall imaging properties contains 75% vinyl pyrrolidone (for example, see ACP- 1001 and ACP-1033 above) . As the % vinyl pyrrolidone decreases, it has been found that the ink receptivity decreases, generally resulting in poor print quality and long ink dry times. More specifically, it has been found that grades containing 75% vinyl pyrrolidone work the best for print quality and ink dry time, while grades containing 50% vinyl pyrrolidone and 50% acrylic acid are marginal, and grades containing 25% vinyl pyrrolidone and 75% acrylic acid do not receive ink at all.
The preferred acrylamide/acrylic acid copolymers are also commercially available. Suitable copolymers can be obtained, for example, from Cytec Industries Inc. of West Patterson, N.J. under the trademark CYANAMER. Conventional crosslinking agents are suitable for use in the present invention. However, the aziridine class of polyfunctional crosslinkers is most preferred for the purposes of the present invention. Suitable aziridine crosslinkers are commercially available, for example, such as crosslinkers CX-100 available from Zeneca Resins of Wilmington, Mass.; XAMA-7 and XAMA-2, both available from Cordova Chemical Co. of North Muskegeon, Michigan. Such polyfunctional crosslinkers generally have a functionality greater than 2, and more preferably in the range of from 2.5 to 3.5.
In general, the amount of crosslinking agent present is an amount sufficient to crosslink the copolymer so as to achieve a water resistance that allows the print to be immersed in water while still maintaining the integrity of the coating, and hence the print. It was determined empirically that from about 3 to about 13% of an aziridine crosslinker, based on the weight of random copolymer, is a preferable amount in terms of print quality and water resistance. More preferably is an amount of from 3 to 5 wt. %, and most preferably from 3 to about 4 wt. %. If too little crosslinker is used, the coatings can be very tacky and not water resistant at all. If too much crosslinker is used, the coating is generally not very receptive to the aqueous inks, and the resulting prints are poor, with much ink pooling and long ink dry times.
Other conventional crosslinkers such as zirconium carbonates can also be used with good results.
The crosslinking of the random copolymer is preferably accomplished during the drying step, for purposes of convenience. It may also be accomplished in a separate step, if preferred. Although the crosslinked copolymers work well as a good water resistant backbone for the coating, they are preferably used in combination with a cationic substance. When prints on a coating containing only the crosslinked resin are immersed in water, the coatings themselves are water resistant, but the ink begins to bleed and leach out of the coating matrix. Since ink jet dyes typically are anionic in nature, a cationic substance is required to "lock" the dyes in the coating matrix. Conventional cationic resins are suitable for use in the coating of the present invention. Quaternary ammonium compounds are preferable, of these, the higher molecular weight compounds are most preferable and provide the best overall print quality and water resistance properties. CPS Chemical Company of Old Bridge, New Jersey manufactures several lines of cationic polymers by the trade name of Agefloc, which are suitable for use in the present invention. Of these, a high molecular weight poly (hydroxyalkene dimethyl ammonium chloride) called Agefloc A-50HV is most preferable with respect to the overall results for print quality and water resistance. Other high molecular weight cationic resins include the Agefloc A- 50 and A-40HV. The amount of cationic material used is generally an amount sufficient to preclude bleeding of the ink when the print is immersed in water, i.e., an ink migration precluding amount. It was empirically determined that preferred print quality and water resistance results are obtained with the use of a formulation containing about 5 to about 10% of the quaternary ammonium resin, as based on the % solids (wt.) of the random copolymer resin. If too little of the quaternary resin is used, the print quality is poor, and the dye runs when immersed in water. If too much of the quaternary resin is used, the initial print quality is poor, and the coatings are tacky.
The receiving layer of the present invention can be coated onto a substrate using any conventional coating process. The coating must generally be dried sufficiently to assure proper crosslinking. For example, it is generally preferred that the coatings be dried at a minimum of 260°F for about 2 minutes to ensure that the crosslinking cures properly. The present invention also includes a process for providing a water resistant ink jet print. The process includes coating a suitable substrate with a vinyl amide acrylic acid or methacrylic acid or ester thereof random copolymer, a cationic resin and a crosslinking agent; curing the coating; and applying droplets of a recording liquid on the coating.
The invention will be illustrated in greater detail by the following specific examples. It is understood that these examples are given by way of illustration and are not meant to limit the disclosure or the claims that follow. All percentages in the examples, and elsewhere in the specification, are by weight unless otherwise specified.
EXAMPLE 1
Syloid 620 0.06g
Deionized water 1.80g
10% Acrylidone ACP-1001 87.70g
28% Ammonium hydroxide 3.75g
Xama 7 0.33g 2-Pyrrolidone 1.09g
50% Agefloc A-50HV 1.75g
The above mix was prepared by mixing the Syloid 620 and water on a magnetic stirring plate for 1 minute. The Acrylidone and ammonium hydroxide were added and the mixture was stirred on the magnetic stirrer for an additional minute. The final three ingredients (2- pyrrolidone, Agefloc A-50HV, Xama 7) were added, and the mixture was stirred for a final five minutes on a magnetic stirring plate. The composition was then coated onto 380 gauge Melinex 534 with a gapped number 70 Mayer rod to achieve a coating thickness of about 0.40 mils. The coating was dried in a laboratory Blue M convection oven for 5 minutes at 260° F. This drying step also resulted in the crosslinking of the Acrylidone copolymer.
The sample was then printed on a Canon BJC600 ink jet printer using a full color block test pattern. Visual densities of cyan, magenta, yellow, black, red, green and blue were run using an XRITE 938 color densitometer. The print was allowed to air dry for 1 hour, then it was completely immersed in water for 10 minutes. The visual densities were repeated after the immersion, and calculations were performed to get the % retained density. The results are summarized in Table 2 below.
EXAMPLE 2
Syloid 620 0.06g
Deionized water 1.80g 10% Acrylidone ACP-1001 78.93g
28% Ammonium hydroxide 3.75g
Xama 7 0.33g
2-Pyrrolidone 1.09g
50% Agefloc A-50HV 1.75g 10% Airvol 325 8.77g
The above mixture was prepared in the same manner as described in Example 1. The Airvol 325 was added after the Agefloc A-50HV and then the mixture was stirred for the final five minutes. The coating, printing, and water immersion were performed in the same manner as in Example 1. The results are summarized in Table 2 below. EXAMPLE 3 Mix B:
10% Gohsenal N-300 20.00g
10% PVP K90 5.00g 40% Zonyl FSJ 0.22g
Water 37. OOg
Example 3 uses two mixes. The first mix (Mix A) was prepared with the same composition as that in Example 1 and applied to the substrate in the same manner as in Example 1. The second mix (Mix B) was prepared in the following manner:
The Gohsenal N-300 and PVP K90 solutions were blended and mixed for 30 seconds on a magnetic stir plate. The Zonyl FSJ and water were added, and stirred for 5 minutes on a magnetic stir plate.
Mix B was then applied as a topcoat onto the coating of that previously prepared according to Example 1 with a wire wound number 10 Mayer rod. The sample was then dried at 240° F in a Blue M convection oven for 2 minutes.
The sample was then printed, tested, and evaluated in the same manner as in Example 1. The results are summarized in Table 2 below.
COMPARATIVE EXAMPLE 1
Syloid 620 0.06g
Deionized water 1.80g
10% Acrylidone ACP-1001 87.70g
28% Ammonium hydroxide 3.75g
2-pyrrolidone 1.09g 50% Agefloc A-50HV 1.75g
The above mixture was prepared in the same manner as described in Example 1. The coating, printing, and water immersion were performed in the same manner as in Example 1. The results are summarized in Table 2 below. COMPARATIVE EXAMPLE 2
Syloid 620 0.06g
Deionized water 1.80g
10% Acrylidone ACP-1001 87.70g 28% Ammonium hydroxide 3.75g
Xama 7 0.33g
2-pyrrolidone 1.09g
The above mixture was prepared in the same manner as described in Example 1. The coating, printing, and water immersion were performed in the same manner as in Example 1. The results are summarized in Table 2 below.
Reagents for the above Examples are commercially available according to the following description:
1) Amorphous silica is available from W.R. Grace, Baltimore, MD as Syloid 620.
2) Vinylpyrrolidone/acrylic acid copolymer is available from International Specialty Polymers of Wayne, NJ as Acrylidone ACP-1001.
3) Aziridine crosslinker is available from Cordova Chemical of North Muskegeon, MI as Xama 7.
4) Poly (Hydroxyalkene Ammonium Chloride) is available from C.P.S. Chemicals of Old Bridge, NJ as Agefloc A-50HV.
5) Fully hydrolyzed polyvinyl alcohol is available from Air Products of Allentown, PA as Airvol 325.
6) Prebonded white polyester is available from ICI Films of Hopewell, VA as Melinex 534.
7) Fully hydrolyzed polyvinyl alcohol is available from Nippon Gohsei Ltd. of Japan as Gohsenal N-300. TABLE 2
PRINT PRINT AVE. % COLOR COMMENTS QUALITY TACK DENSITY
RETENTION
EXAMPLE 1 Very Good Moderate 99.9% Vibrant colors/Good wet rub resistance
EXAMPLE 2 Very Good Low 98.8% Vibrant colors/Good wet rub resistance
EXAMPLE 3 Very Good Very Low 99.0% Vibrant Colors/ Glossy Finish/Very low print tack
COMPARATIVE Good Very High 0 % Coating Washed EXAMPLE 1 Off
COMPARATIVE Poor Moderate 107% High High color EXAMPLE 2 to High bleed causes bleed/High Ink increased coalescence retention
Examples 1 and 2 both had very good print quality and excellent water resistance properties. When a small amount of a fully hydrolyzed polyvinyl alcohol is added, as in Example 2, the print tack is reduced significantly. The print tack can be reduced even further, and the colors can be made very glossy, by adding a thin PVP/fully hydrolyzed polyvinyl alcohol topcoat as seen in Example 3. In general, the addition or use of small amounts of additional resins, such as polyvinyl alcohol or an acrylic resin, can be employed to improve print quality. When no crosslinker is used, as in Comparative
Example 1, the resulting coating is very tacky, and is easily dissolved in water. When the high MW quaternary ammonium resin is eliminated from the mix, as in Comparative Example 2, the print quality is poor indicating a high amount of bleed and ink pooling. Thus, to achieve an ink jet recording medium which exhibits excellent water resistance and a freedom from migration or leaching, the combination of the random copolymer together with the crosslinker and the cationic resin is important.
EXAMPLE 4
Syloid 620 0.06g
Deionized water 62.92g Cyanamer P-21 6.99g
28% Ammonium hydroxide 2.93g
CX 0.29 g
2-pyrrolidone 0.85g
50% Agefloc A-50HV 0.75g 50% Fluorad FC-135 0.14g
20% Gafquat 755N 25.08g
The above mixture was prepared by mixing the Syloid
620 and water on a magnetic stirring plate for 1 minute.
The Cyanamer was slowly added, and stirred for 15 minutes. The ammonium hydroxide was added and the mixture was stirred for a final fifteen minutes on a magnetic stirring plate.
The composition was then coated onto 380 gauge Melinex 534 with a gapped number 70 Mayer rod to achieve a coating thickness of about 0.40 mils. The coating was dried in a laboratory Blue M convection oven for 5 minutes at 260 F.
The samples were then printed on a Canon BJC600e ink jet printer, and an Encad NovaJet ink jet printer using a full color block test pattern. The print was allowed to air dry for 1 hour, then it was completely immersed in water for 10 minutes. The print quality, evaluated as in Example 1, water immersion and wet rub resistance were all very good. The reagents used in the foregoing Example are commercially available and may be generally described as follows:
Syloid 620 — amorphous silica from W.R. Grace, Baltimore, Md.
Cyanamer P-21 — acrylamide/acrylic acid copolymer from Cytec Industries Inc. of West Patterson, N.J.
CX-100 — aziridine cross linker from Zeneca Resins of Wilmington, Ma. Agefloc A-50HV — poly(Hydroxyalkene ammonium chloride) from C.P.S. Chemicals of Old Bridge, N.J.
Fluorad FC-135 — cationic fluorosurfactant from 3M of St. Paul, Minnesota
Gafquat 755N — quaternized copolymer of vinylpyrrolidone and dimethylaminoethyl methacrylate from International Specialty Products of Wayne, N.J.
Melinex 534 — prebonded white polyester from ICI Films of Hopewell, Va.
While the invention has been described with preferred embodiments, it is to be understood that variations and modifications may be resorted to as will be apparent to those skilled in the art. Such variations and modifications are to be considered within the purview and the scope of the claims appended thereto.

Claims

WHAT IS CLAIMED IS:
1. An ink jet receiving medium having an ink receptive coating comprised of a random copolymer of a vinyl amide and an acrylic or methacrylic acid or an ester thereof, a cationic resin and a crosslinking agent.
2. The ink jet receiving medium of Claim 1, wherein the random copolymer is a copolymer comprised of vinyl pyrrolidone.
3. The ink jet receiving medium of Claim 2, wherein the random copolymer is a copolymer comprised of acrylic acid.
4. The ink jet receiving medium of Claim 1, wherein the random copolymer is a copolymer comprised of acrylamide.
5. The ink jet receiving medium of Claim 4, wherein the random copolymer is a copolymer comprised of acrylic acid.
6. The ink jet receiving medium of Claim 1, wherein said vinyl pyrrolidone/acrylic acid random copolymer is comprised of 75% vinyl pyrrolidone and 25% acrylic acid.
7. The ink jet receiving medium of Claim 1, wherein said crosslinking agent is present in an amount of from 3 to 4% by weight, as based on the random copolymer.
8. The ink jet receiving medium of Claim 1, further comprising a substrate which is a clear film, a polyethylene clad paper, adhesive backed vinyl, paper or canvas.
9. The ink jet receiving medium of Claim 1, which is obtained upon crosslinking the random copolymer.
10. An ink jet receiving medium comprising a substrate, an ink jet ink receptive coating on said substance comprised of a crosslinked vinyl acrylic acid or methacrylic acid or ester thereof random copolymer and a cationic resin.
11. The ink jet receiving medium of Claim 10, wherein the random copolymer is a copolymer comprised of vinyl pyrrolidone.
12. The ink jet receiving medium of Claim 11, wherein the random copolymer is a copolymer comprised of acrylic acid.
13. The ink jet receiving medium of Claim 10, wherein the random copolymer is a copolymer comprised of acrylamide.
14. The ink jet receiving medium of Claim 13, wherein the random copolymer is a copolymer comprised of acrylic acid.
15. A water resistant ink jet print comprising a substrate, an ink receptive coating on said substrate with said coating comprising a crosslinked vinyl amide acrylic acid or methacrylic acid or ester thereof random copolymer and a cationic resin; and, an image on said ink receptive coating.
16. The ink jet receiving medium of Claim 15, wherein the random copolymer is a copolymer comprised of vinyl pyrrolidone.
17. The ink jet receiving medium of Claim 16, wherein the random copolymer is a copolymer comprised of acrylic acid.
18. The ink jet receiving medium of Claim 15, wherein the random copolymer is a copolymer comprised of acrylamide.
19. The ink jet receiving medium of Claim 18, wherein the random copolymer is a copolymer comprised of acrylic acid.
20. A process for providing a water resistant ink jet print comprising attaching droplets of an aqueous recording ink containing a water-soluble dye to a receiving medium comprising an ink receiving layer provided on a substrate, the ink receiving layer comprising a crosslinked vinyl acrylic acid or methacrylic acid or ester thereof random copolymer and a cationic resin.
PCT/US1995/016371 1994-12-14 1995-12-13 Aqueous ink receptive ink jet receiving medium yielding a water resistant ink jet print WO1996018496A1 (en)

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DE69519392T DE69519392T2 (en) 1994-12-14 1995-12-13 AQUEOUS INK RECORDING INK JET RECEIVING MEDIUM, WHICH GIVES A WATER RESISTANT INK JET PRINT
AT95944618T ATE197425T1 (en) 1994-12-14 1995-12-13 AQUEOUS INK RECEPTION INKJET RECEIVING MEDIUM WHICH RESULTS IN A WATER RESISTANT INKJET PRINT
EP95944618A EP0801602B1 (en) 1994-12-14 1995-12-13 Aqueous ink receptive ink jet receiving medium yielding a water resistant ink jet print
JP51928196A JP2001520591A (en) 1994-12-14 1995-12-13 Aqueous ink-receptive inkjet receiving medium for providing water-resistant inkjet prints
AU47393/96A AU4739396A (en) 1994-12-14 1995-12-13 Aqueous ink receptive ink jet receiving medium yielding a water resistant ink jet print

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WO1998056591A1 (en) * 1997-06-13 1998-12-17 Ppg Industries Ohio, Inc. Coating composition and printing medium
EP0890445A1 (en) * 1997-07-08 1999-01-13 Sony Chemicals Corporation Recording sheets
WO1999065701A1 (en) * 1998-06-19 1999-12-23 Minnesota Mining And Manufacturing Company Inkjet receptor medium having ink migration inhibitor and method of making and using same
WO2000063023A1 (en) * 1999-04-16 2000-10-26 3M Innovative Properties Company Inkjet receptor medium having a multi-staged ink migration inhibitor
US6183844B1 (en) 1998-12-16 2001-02-06 Hewlett-Packard Company Inkjet printing medium comprising multiple coatings
US6194077B1 (en) 1997-11-06 2001-02-27 Arkwright Incorporated Waterfast ink receptive material
US6383612B1 (en) 1998-06-19 2002-05-07 3M Innovative Properties Company Ink-drying agents for inkjet receptor media
US6514600B1 (en) 2000-05-18 2003-02-04 Isp Investments Inc. Color inkjet receptive films having long term light stability
US6632510B1 (en) 1997-07-14 2003-10-14 3M Innovative Properties Company Microporous inkjet receptors containing both a pigment management system and a fluid management system
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US6682247B1 (en) 2000-06-30 2004-01-27 Avery Dennsion Corporation Drawable and/or traceable carriers
US6703112B1 (en) 1998-06-19 2004-03-09 3M Innovative Properties Company Organometallic salts for inkjet receptor media
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EP0738608A3 (en) * 1995-04-20 1997-11-19 Canon Kabushiki Kaisha Curable compositions and their use for the formation of a printing material
US6340725B1 (en) 1997-06-13 2002-01-22 Hewlett-Packard Company Inkjet printing media
US6074761A (en) * 1997-06-13 2000-06-13 Ppg Industries Ohio, Inc. Inkjet printing media
WO1998056591A1 (en) * 1997-06-13 1998-12-17 Ppg Industries Ohio, Inc. Coating composition and printing medium
US6238797B1 (en) 1997-07-08 2001-05-29 Sony Chemicals Corporation Recording sheets
EP0890445A1 (en) * 1997-07-08 1999-01-13 Sony Chemicals Corporation Recording sheets
US6632510B1 (en) 1997-07-14 2003-10-14 3M Innovative Properties Company Microporous inkjet receptors containing both a pigment management system and a fluid management system
US6194077B1 (en) 1997-11-06 2001-02-27 Arkwright Incorporated Waterfast ink receptive material
US6537650B1 (en) 1998-06-19 2003-03-25 3M Innovative Properties Company Inkjet receptor medium having ink migration inhibitor and method of making and using same
WO1999065701A1 (en) * 1998-06-19 1999-12-23 Minnesota Mining And Manufacturing Company Inkjet receptor medium having ink migration inhibitor and method of making and using same
US6703112B1 (en) 1998-06-19 2004-03-09 3M Innovative Properties Company Organometallic salts for inkjet receptor media
US6383612B1 (en) 1998-06-19 2002-05-07 3M Innovative Properties Company Ink-drying agents for inkjet receptor media
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US6183844B1 (en) 1998-12-16 2001-02-06 Hewlett-Packard Company Inkjet printing medium comprising multiple coatings
US6677007B1 (en) 1999-02-12 2004-01-13 3M Innovative Properties Company Image receptor medium and method of making and using same
US6514599B1 (en) 1999-04-16 2003-02-04 3M Innovative Properties Company Inkjet receptor medium having a multi-staged ink migration inhibitor and method of making and using same
WO2000063023A1 (en) * 1999-04-16 2000-10-26 3M Innovative Properties Company Inkjet receptor medium having a multi-staged ink migration inhibitor
US6514600B1 (en) 2000-05-18 2003-02-04 Isp Investments Inc. Color inkjet receptive films having long term light stability
US6682247B1 (en) 2000-06-30 2004-01-27 Avery Dennsion Corporation Drawable and/or traceable carriers
WO2003097730A2 (en) 2001-06-14 2003-11-27 Avery Dennison Corporation Photo album
US6808776B2 (en) 2002-03-11 2004-10-26 Avery Dennison Corporation Water-absorbent film construction
US6846531B2 (en) 2002-03-11 2005-01-25 Avery Dennison Corporation Water-absorbent film construction

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ATE197425T1 (en) 2000-11-11
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AU4739396A (en) 1996-07-03

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