Field ofthe Invention The invention relates to a noncrosslinked composition suitable for use as an ink-jet recording medium, and a polymeric recording sheet coated with such compositions and subsequently crosslinked, such sheet being suitable for imaging in an ink-jet printer.

Description ofthe Art Imaging devices such as ink-jet printers and pen plotters are established methods for printing various information including labels and multi-color graphics. Presentation of such information has created a demand for ink receptive imageable receptors, especially transparent receptors, that are used as overlays in technical drawings and as transparencies for overhead projection. Imaging with either the ink- jet printer or the pen plotter involves depositing ink on the surface of these transparent receptors. These imaging devices conventionally utilize inks that can remain exposed to air for long periods of time without completely drying. Since it is desirable that the surface of these receptors be dry and non-tacky to the touch soon after imaging, even after absorption of significant amounts of liquid, it is desirable that transparent materials for imaging be capable of absorbing significant amounts of liquid while maintaining some degree of durability and transparency. Generation of an image by an ink-jet printer results in large quantities of solvent, generally blends of glycols and water, remaining in the imaged areas. Diffusion of this solvent into unimaged areas can result in "bleeding" ofthe image, when the dye is carried along with the solvent.

U.S. Patent 5,141,797 discloses opaque ink-jet recording sheets including a water soluble polymeric binder, a titanium chelate crosslinking agent, and an inorganic filler with a high absoφtion capacity, e.g., silica. The filler is present in a ratio to polymeric binder of from 2:1 to 7: 1. Paper substrates are preferred. Only single layer coatings are disclosed.

Liquid-absorbent materials disclosed in U.S. Patent No. 5,134,198 disclose one method to improve drying and decrease dry time. These materials comprise

crosslinked polymeric compositions capable of forming continuous matrices for liquid absorbent semi-interpenetrating polymer networks. These networks are blends of polymers wherein at least one ofthe polymeric components is crosslinked after blending to form a continuous network throughout the bulk ofthe material, and through which the uncrosslinked polymeric components are intertwined in such a way as to form a macroscopically homogenous composition. Such compositions are useful for forming durable, ink absorbent, transparent graphical materials without the disadvantages ofthe materials listed above.

WO 8806532 discloses a recording transparency and an aqueous method of preparation. The transparency is coated with a hydroxyethylcellulose polymer or mixture of polymers. The coating solution may also contain a surfactant to promote leveling and adhesion to the surface, and hydrated alumina in order to impart pencil tooth to the surface.

U.S. Patent No. 5,277,965 discloses a recording medium comprising a base sheet with an ink receiving layer on one surface, and a heat absorbing layer on the other, and an anti-curl layer coated on the surface ofthe heat absorbing layer. The materials suitable for the ink receptive layer can include hydrophilic materials such as binary blends of polyethylene oxide with one ofthe following group: hydroxypropyl methyl cellulose (Methocel), hydroxyethyl cellulose; water-soluble ethylhydroxyethyl cellulose, hydroxybutylmethyl cellulose, hydroxypropyl cellulose, methyl cellulose, hydroxyethylmethyl cellulose; vinylmethyl ether/maleic acid copolymers; acrylamide/acrylic acid copolymers; salts of carboxymethylhydroxyethyl cellulose; cellulose acetate; cellulose acetate hydrogen phthalate, hydroxypropyl methyl cellulose phthalate; cellulose sulfate; PVA; PVP; vinyl alcohol/vinylacetate copolymer and so on.

U.S. Patent No. 5,068,140 discloses a transparency comprised of a supporting substrate and an anticurl coating or coatings thereunder. In one specific embodiment, the transparency comprises of an anticurl coating comprising two layers. The ink receiving layer in one embodiment is comprised of blends of po!y(ethylene oxide), mixtures of poly(ethylene oxide) with cellulose such as sodium carboxymethyl cellulose, hydroxymethyl cellulose and a component selected from the group consisting of (1) vinylmethyl ether/maleic acid copolymer; (2) hydroxypropyl cellulose;

(3) acrylamide/acrylic acid copolymer, (4) sodium carboxymethylhydroxyethyl cellulose; (5) hydroxyethyl cellulose; (6) water soluble ethylhydroxyethyl cellulose; (7) cellulose sulfate; (8) poly(vinyl alcohol); (9) polyvinyl pyrrolidone; (10) poly(acrylamido 2-methyl propane sulfonic acid); (11) poly(diethylenetriamine-co- adipic acid); (12) poly(imidazoline) quatemized; (13) poly(N,N-methyl-3-S dimethylene piperidinum chloride; (14) poly(ethylene imine)epichlorohydrin modified; (15) poly(ethylene imine) ethoxylated; blends of poly(α-methylstyrene) with a component having a chlorinated compound.

U.S. Patent No. 4,554,181, discloses a recording sheet for ink-jet printing having a single layer coated on a substrate. The coating, which may be on paper or film substrates, contains two key components; a mordant, and a water soluble polyvalent metal salt. The mordant is a cationic polymer material, designed to react with an acid group present on a dye molecule. The water soluble polyvalent metal salt may be from a wide selection of metals, those of group II, group III, and the transition metals ofthe periodic table of elements. Specific salts mentioned include calcium formate, aluminum chlorohydrate, and certain zirconium salts. A two-layer system is not disclosed.

U.S. Patent No. 4,141,797, discloses ink-jet papers having crosslinked binders, and opaque sheets. The opacity is achieved by using a paper stock, and by including an inorganic filler in the coated layer. An titanium chelate cross linking agent is also disclosed. Tyzor® TE is specifically mentioned. Three other patents disclose the generic use of titanium compounds as cross-linking agents, i.e., U.S. Patent Nos. 4,609,479, 3,682,688, and 4,690,479. Binder polymers, including gelatin materials, are disclosed, as is use of a mordant. U.S. Patent No. 4,781,985 discloses a film support having a coating thereon, such coating containing one of two possible general structures of ionic fluorocarbon surfactants. One of these two general structures is characterized by a quaternary ammonium compound having a side chain containing a sulfide linkage; the other general structure contains the element phosphorus. It is disclosed that other fluorochemical surfactants will not provide the benefits of these two structures. No two layer coating systems are disclosed.

U.S. Patent No. 5,429,860 discloses an ink/media combination, with a purpose to arrive at a superior final copy by designing the ink to match the film, and vice-versa. An external energy source is used to effect a fix step after the ink has been brought in contact with the medium. At least one multivalent metal salt, Tyzor® 131, is disclosed, as are generic organic titanates.

U.S. Patent Nos. 5,045,864 and US 5,084,340, disclose a single layer image- recording elements comprising an ink receptive layer including containing 50-80 percent of a specific polyester particulate material, i.e., poly(cyclohexylenedimethylene-co-oxydiethelene isophthalate-co-sodio- sulfobenzenedicarboxyolates), 15-50% vinyl pyrrolidone, and minor amounts of a short chain alkylene oxide homopolymer or copolymer, a fluorochemical surfactant and inert particles.

The present inventors have now discovered that an inkjet film comprising a single layer, or a thick absoφtive underlayer, and an optically clear thin top layer containing certain nonionic surfactants and a metal chelate provides high density images which are tack-free and permanent, and which have substantially no color bleed.

Summary ofthe Invention The invention provides a composition suitable for use on an ink-jet recording sheet, an ink-jet recording sheet having said composition coated onto at least one major surface, and an ink-jet recording sheet having a two layer coating structure. Compositions ofthe invention comprise a) at least one nonionic fluorocarbon surfactant b) at least one metal chelate wherein said metal is selected from the group consisting of titanium, zirconium, and aluminum, c) at least one polymer selected from the group consisting of hydroxycellulose and substituted hydroxycellulose polymers, such composition being crosslinkable when subjected to temperatures of at least about 90°C. Ink-jet recording sheets ofthe invention comprise a substrate having two major surfaces, at least one major surface having coated thereon a composition comprising a

nonionic fluorocarbon surfactant, at least one metal chelate selected from the group consisting of titanium, zirconium and aluminum metal chelates, and at least one polymer selected from the group consisting of hydroxycellulose and substituted hydroxycellulose polymers, said composition having been crosslinked on said substrate.

Preferred ink-jet recording sheets ofthe invention comprise a ink-jet recording sheet comprising a two-layer imageable coating comprising: a) a thick absoφtive bottom layer comprising at least one crosslinkable polymeric component, and b) an optically clear, thin top layer comprising at least one nonionic fluorocarbon surfactant, and at least one metal chelate wherein said metal is selected from the group consisting of titanium, aluminum and zirconium, said top layer having been crosslinked on said substrate by heat. Preferred two-layer coatings comprise a) a thick absoφtive bottom layer comprising i) at least one crosslinkable polymeric component; ii) at least one liquid-absorbent component comprising a water- absorbent polymer, and iii) from 0 to 5% of a crosslinking agent b) an optically clear, thin top layer comprising i) from 0.05% to 6% of at least one nonionic fluorocarbon surfactant, ii) from 14% to 94% of a hydroxycellulose or substituted hydroxycellulose polymer, iii) from 5% to 80% of an alkanolamine metal chelate.

The following terms have these meanings as used herein:

1. The term "semi-inteφenetrating network" means an entanglement of a homocrosslinked polymer with a linear uncrosslinked polymer.

2. The term "SIPN" refers to a semi-inteφenetrating network. 3. The term "mordant" means a compound which, when present in a composition, interacts with a dye to prevent diffusion through the composition.

4. The term "crosslinkable" means capable of forming covalent or strong ionic bonds with itself or with a separate agent added for this puφose.

5. The term "hydrophilic" is used to describe a material that is generally receptive to water, either in the sense that its surface is wettable by water or in the sense that the bulk ofthe material is able to absorb significant quantities of water. Materials that exhibit surface wettability by water have hydrophilic surfaces. Monomeric units will be referred to as hydrophilic units if they have a water-soφtion capacity of at least one mole of water per mole of monomeric unit.

6. The term "hydrophobic" refers to materials which have surfaces not readily wettable by water. Monomeric units will be referred to as hydrophobic if they form water-insoluble polymers capable of absorbing only small amounts of water when polymerized by themselves.

7. The term "chelate" means a coordination compound in which a central metal ion is attached by coordinate links to two or more nonmetal ligands, which form heterocyclic rings with the metal ion being a part of each ring.

8. The term "surfactant" means a compound which reduces surface tension, thereby increasing surface wetting.

9. The term "optically clear" means that the majority of light passing through does not scatter. All parts, percents and ratios herein are by weight, unless specifically stated otherwise.

Detailed Description ofthe Invention Compositions ofthe invention are suitable for coating onto ink-jet recording sheets. Such compositions are crosslinkable with the application of heat, and comprise at least one aluminum, zirconium, or titanium metal chelate, at least one nonionic fluorocarbon surfactant, and at least one cellulose material selected from the group consisting of hydroxycellulose and substituted hydroxycellulose polymers, such composition being crosslinkable when subjected to temperatures of at least about 90°C. Useful metal chelates include titanate chelates, zirconate chelates and aluminum chelates. Such chelates typically do not undergo immediate hydrolysis when mixed

with crosslinkable materials, but will remain unreactive unless activated by raising the temperature which causes the structure ofthe chelate to begin breaking down. The exact temperature required will depend on the activity ofthe other ingredients with which the chelate is mixed, and the functional groups on the metal chelate. Useful functional groups include esters, amines, acetonates, and the like, .e.g., triethanolamine metal chelates and acetyl acetonate chelates. Chelates containing aluminum and titanate are preferred, with triethanolamine titanate chelates being highly preferred.

It is believed that the metal chelates do not undergo solvolysis when combined with the other ingredients, but rather begin to crosslink when heated during film drying. The chelates are complexed, the chelates provide titanate metal ions which are then complexed with a hydroxycellulose material, and are converted to the corresponding metal oxide or hydroxide in the cellulose matrix. The metal ions then undergo further reaction with the alkanolamine which regenerates the titanate alkanolamine chelates in hydroxylate form. The solvolysis profile is shown below:

HPMC +H?Q +M-TE

(Coating ^" System)

)

[M(OH)2(H ₂ O)4]+n

MO2. nH2θ M(OH) _x . nH2θ [M/MOJ+n Cross-links with HPMC

Commercially available chelates include triethanolamine titanate chelates, available as Tyzor® TE; ethyl acetoacetate titanate chelate, Tyzor® DC; lactic acid titanate chelate, Tyzor® LA and acetylacetonate titanate chelate, Tyzor® GBA, available from E.I. DuPont de Nemours (DuPont).

Useful nonionic fluorocarbon surfactants are those having at least a weakly hydrophilic portion and a hydrophobic portion. Useful surfactants include linear perfluorinated polyethoxylated alcohols, fluorinated alkyl polyoxyethylene alcohols, and fluorinated alkyl alkoxylates.

Preferred nonionic fluorocarbon surfactants are those having a strongly hydrophilic end and a strongly hydrophobic end. The hydrophobic end allows effective blooming to the surface ofthe coated layer, and the hydrophilic end provides a high

surface energy moiety on the surface which interacts with water-based inks to give uniform images. Preferred surfactants are fluorinated polyethoxylated alcohols.

Commercially available nonionic surfactants include fluorochemical surfactants such as the perfluorinated polyethoxylated alcohols available as Zonyl FSO®, Zonyl FSN®, and the 100% pure versions thereof Zonyl FSO-lOO®, having the following structure,

RfCH ₂ CH2(CH2CH ₂ O) ₁ - ₁₈ OH

Rf = F(CF ₂ CF ₂ )2-ιo and Zonyl FSN- 100®, from DuPont; and the fluorinated alkyl polyoxyethylene alcohols available as Fluorad® FC-170C, having the following structure:

and Fluorad® 171C, available from Minnesota Mining and Manufacturing Company (3M), which can be represented as the following:

While the preferred level will vary with the particular nonionic fluorocarbon surfactant used, compositions ofthe invention typically comprise up to 10%, preferably from 0.05% to 6% of said surfactant. When a fluorocarbon surfactant comprising a polyethoxylated alcohol is used, the composition preferably comprises from 0.5% to 3% percent ofthe composition.

Ink-jet recording sheets ofthe inventions comprise a substrate having coated thereon a single layer which comprises the essential ingredients of compositions ofthe invention. Single-layer compositions ofthe invention must comprise at least one metal chelate wherein the metal is selected from the group consisting of zirconium, titanate and aluminum, at least one nonionic fluorocarbon surfactant, and at least one cellulose material selected from the group consisting of hydroxycellulose and substituted hydroxycellulose polymers.

The composition is not crosslinked prior to coating onto the sheet, but is coated as the uncrosslinked composition described supra, and after coating, is crosslinked by the application of heat. This is typically done in a dry-ng oven. While not wishing to be bound by theory, it is believed that the nonionic fluorosurfactant blooms to the surface after coating. Some aging ofthe recording sheet is therefore preferred. This provides improved optical density properties, as well as allowing the hydrophilic portion ofthe surfactant to convey the large ink-drops used in ink-jet imaging through the layer where it can be absorbed. If the composition were crosslinked prior to coating, the surfactant would be trapped within the crosslinked network, requiring a much higher concentration in order for any to be present on the surface.

Preferred single-layer ink-jet recording sheets ofthe invention comprise from 0.5% to 6% percent of a nonionic fluorocarbon surfactant, from 5% to 80% ofthe metal chelate and at least one cellulosic polymer selected from the group consisting of hydroxycellulose and substituted hydroxycellulose polymers, such as hydroxyethyl cellulose, hydroxypropylmethylcellulose and the like.

Such single-layer coating may also include additional adjuvants such as mordants, polymeric microspheres, anticurling agents such as polyethylene glycols, and the like. Preferred ink-jet recording sheets ofthe invention comprise a two layer coating system including an optically clear top layer, and an ink-absoφtive underlayer.

The top layer is an optically clear, thin layer comprising at least one nonionic fluorocarbon surfactant, an alkanolamine metal chelate, and at least one hydroxycellulose or substituted hydroxycellulose polymer, as described, supra. Top layers ofthe invention comprise from 5% to 80% ofthe metal chelate, preferably from 5% to 35% percent.

The top layer also comprises at least 14% to 94% of a hydroxycellulose polymer. Useful hydroxycellulosic materials include hydroxymethyl- cellulose, hydroxypropylcellulose and hydroxyethyl-cellulose and the like. Such materials are available commercially, e.g., as Methocel® series denoted A, E, F, J, K and the like, e.g., Methocel® F-50, from Dow Chemical Company.

The top layer may also includes particulates, such as polymeric microspheres or beads, which may be hollow or solid, for the puφose of improving handling and flexibility. Preferred particulate materials are formed form polymeric materials such as poly(methylmethacrylate), poly(stearyl methacrylate)hexanedioldiacrylate copolymers, polytetrafluoroethylene), polyethylene; starch and silica. Poly(methylmethacrylate) beads are most preferred. Levels of particulate are limited by the requirement that the final coating be transparent with a haze level of 15% or less, as measured according to ASTM D1003-61 (Reapproved 1979). The preferred mean particle diameter for particulate material is from 5 to 40 micrometers, with at least 25% ofthe particles having a diameter of 15 micrometers or more. Most preferably, at least about 50% of the particulate material has a diameter of from 20 micrometers to 40 micrometers.

The absoφtive underlayer comprises a polymeric ink-receptive material. Although at least one ofthe polymers present in the polymeric ink-receptive material is preferably crosslinkable, the system need not be crosslinked to exhibit the improved longevity and reduced bleeding. Such crosslinked systems have advantages for dry time, as disclosed in U.S. Patent 5,134,198 (Iqbal).

Preferably the underlayer comprises a polymeric blend containing at least one water-absorbing, hydrophilic, polymeric material, and at least one hydrophobic polymeric material incoφorating acid functional groups. Soφtion capacities of various monomeric units are given, for example, in D. W. Van Krevelin, with the collaboration of P. J. Hoftyzer, Properties of Polymers: Correlations with Chemical Structure, Elsevier Publishing Company (Amsterdam, London, New York, 1972), pages 294-296. Commercially available polymers include "Copolymer 958", a poly(vinylpyrrolidone/dimethylaminoethylmethacrylate), available from GAF Coφoration, and the like.

The water-absorbing hydrophilic polymeric material comprises homopolymers or copolymers of monomeric units selected from vinyl lactams, alkyl tertiary amino alkyl acrylates or methacrylates, alkyl quaternary amino alkyl acrylates or methacrylates, 2-vinylpyridine and 4-vinylpyridine. Polymerization of these monomers can be conducted by free-radical techniques with conditions such as time, temperature, proportions of monomeric units, and the like, adjusted to obtain the desired properties ofthe final polymer.

Hydrophobic polymeric materials are preferably derived from combinations of acrylic or other hydrophobic ethylenically unsaturated monomeric units copolymerized with monomeric units having acid functionality. The hydrophobic monomeric units are capable of forming water-insoluble polymers when polymerized alone, and contain no pendant alkyl groups having more than 10 carbon atoms. They also are capable of being copolymerized with at least one species of acid-functional monomeric unit.

Preferred hydrophobic monomeric units are preferably selected from certain acrylates and methacrylates, e.g., methyl(meth)acrylate, ethyl(meth)acrylate, acrylonitrile, styrene or a-methylstyrene, and vinyl acetate. Preferred acid functional monomeric units for polymerization with the hydrophobic monomeric units are acrylic acid and methacrylic acid in amounts of from 2% to 20%.

In a preferred embodiment, the underlayer coating is a semi-inteφenetrating network (SIPN). The SIPN ofthe present invention comprises crosslinkable polymers that are either hydrophobic or hydrophilic in nature, and can be derived from the copolymerization of acrylic or other hydrophobic or hydrophilic ethylenically unsaturated monomeric units with monomers having acidic groups, or if pendant ester groups are already present in these acrylic or ethylenically unsaturated monomeric units, by hydrolysis. The SIPN for this ink-receptive coating would be formed from polymer blends comprising at least one crosslinkable polyethylene-acrylic acid copolymer, at least one hydrophilic liquid absorbent polymer, and optionally, a crosslinking agent. The SLPNs are continuous networks wherein the crosslinked polymer forms a continuous matrix, as disclosed in U.S. Patents 5,389,723, 5,241,006, 5,376,727.

Preferred SLPNs to be used for forming underlayer layers ofthe present invention comprise from 25 to 99 percent crosslinkable polymer, preferably from 30 to 60 percent. The liquid-absorbent component can comprise from 1 to 75 percent, preferably from 40 to 70 percent ofthe total SLPNs.

The crosslinking agent is preferably selected from the group of polyfunctional aziridines possessing at least two crosslinking sites per molecule, such as trimethylol propane-tris-(β-(N-aziridinyl)propionate),

pentaerythritol-tris-(β-(N-aziridinyl)propionate),

II ^ ^* ^ ²

OH-CH2 -C - (CH ₂ — O — C - CH2 — O-^— -Nl I )

CH2 3 trimethylolpropane-tris-(β-(N-methylaziridinyl propionate)

and so on. When used, the crosslinking agent typically comprises from 0.5 to 6.0 percent crosslinking agent, preferably from 1.0 to 4.5 percent.

The underlayer may also comprise a mordant for reduction of ink fade and bleed. When present, the mordant preferably comprises from 1 part by weight to 20 parts by weight ofthe solids, preferably from 3 parts by weight to 10 parts by weight. Useful mordants include polymeric mordants having at least one guanidine functionality.

The underlayer formulation can be prepared by dissolving the components in a common solvent. Well-known methods for selecting a common solvent make use of Hansen parameters, as described in U.S. 4,935,307.

The two layers can be applied to the film substrate by any conventional coating technique, e.g., deposition from a solution or dispersion ofthe resins in a solvent or aqueous medium, or blend thereof, by means of such processes as Meyer bar coating, knife coating, reverse roll coating, rotogravure coating, and the like. The base layer is preferably coated to a thickness of from 0.5 μm to 10 μm, and the top layer preferably has a thickness of from 0.5 μm to 10 μm.

Drying ofthe layers can be effected by conventional drying techniques, e.g., by heating in a hot air oven at a temperature appropriate for the specific film substrate chosen. However, the drying temperature must be at least about 90°C, preferably at

least about 120°C in order to crosslink the metal chelate and form the colloidal gel with the hydroxycellulose polymer.

Additional additives can also be incoφorated into either laye- to improve processing, including thickeners such as xanthan gum, catalysts, thickeners, adhesion promoters, glycols, defoamers, antistatic materials, and the like. Likewise, additives such as the mordant, may be present in the top layer rather than the base layer or in both layers. An additive which may be present in the underlayer to control curl is a plasticizing compound. Useful compounds include, e.g., low molecular weight polyethylene glycols, polypropylene glycols, or polyethers; for example PEG 600, Pycal® 94, and Carbowax® 600.

Film substrates may be formed from any polymer capable of forming a self- supporting sheet, e.g., films of cellulose esters such as cellulose triacetate or diacetate, polystyrene, polyamides, vinyl chloride polymers and copolymers, polyolefin and polyallomer polymers and copolymers, polysulphones, polycarbonates and polyesters. Suitable polyester films may be produced from polyesters obtained by condensing one or more dicarboxylic acids or their lower alkyl diesters in which the alkyl group contains up to 6 carbon atoms, e.g., terephthalic acid, isophthalic, phthalic, 2,5-,2, 6-, and 2,7-naphthalene dicarboxylic acid, succinic acid, sebacic acid, adipic acid, azelaic acid, with one or more glycols such as ethylene glycol, 1,3 -propanediol, 1,4- butanediol, and the like.

Preferred film substrates are cellulose triacetate or cellulose diacetate, polyesters, especially poly(ethylene terephthalate), and polystyrene films. Poly(ethylene terephthalate) is most preferred. It is preferred that film substrates have a caliper ranging from 50 micrometers to 125 micrometers. Film substrates having a caliper of less than 50 micrometers are difficult to handle using conventional methods for graphic materials. Film substrates having calipers over 125 micrometers are very stiff, and present feeding difficulties in certain commercially available ink-jet printers and pen plotters.

Substrates may be opaque, transparent or translucent depending on the intended use, e.g., transmissive projection, reflective projections, or individual copies intended for brochures and the like. Where an opaque substrate is desired, the

substrate may be a film as described above, with pigmented fillers, or it may be a microvoided surface such as a paper or cloth surface.

When polyester or polystyrene film substrates are used, they are preferably biaxially oriented, and may also be heat set for dimensional stability during fusion of the image to the support. These films may be produced by any conventional method in which the film is biaxially stretched to impart molecular orientation and is dimensionally stabilized by heat setting.

To promote adhesion ofthe underlayer to the film substrate, it may be desirable to treat the surface ofthe film substrate with one or more primers, in single or multiple layers. Useful primers include those known to have a swelling effect on the film substrate polymer. Examples include halogenated phenols dissolved in organic solvents. Altematively, the surface ofthe film substrate may be modified by treatment such as corona treatment or plasma treatment.

The primer layer, when used, should be relatively thin, preferably less than 2 micrometers, most preferably less than 1 micrometer, and may be coated by conventional coating methods.

Transparencies ofthe invention are particularly useful in the production of imaged transparencies for viewing in a transmission mode, e.g., in association with an overhead projector. The following examples are for illustrative puφoses, and do not limit the scope ofthe invention, which is that defined by the claims.

Test Methods Image Density The transmissive image density is measured by imaging the color desired, and measuring using a Macbeth TD 903 densitometer with the gold and status A filters. Black image density is evaluated by measuring the density of a solid fill black rectangle image.

Dry Time The environmental conditions for this test are 70°C and 50% relative humidity (RH). The print pattem consists ofsolid fill columns of adjacent colors. The columns

are 0.64 cm to 1.27 cm wide, and 15-23 centimeters long. After printing the material is placed on a flat surface, then placed in contact with bond paper. A 2 kg rubber roller 6.3 cm wide is then twice rolled over the paper. The paper is then removed, and the dry time, Dr is calculated by using the following formula: where TD is the length of time between the end ofthe printing and placing the image in contact with the bond paper; L-r is the length of image transfer to paper; L _P is the length ofthe printed columns; and Tp is the time of printing.

Surface Energy Surface energy values are tested using a Wilhelmy balance, model DCA-322.

The testing is done at ambient room temperature, and the balance is operated at a rate of 136 microns/minute over a distance of 20 mm.

The samples are prepared by cutting two pieces of coated film, placing adhesive on the back of one piece using Scotch® Permanent Adhesive Glue Stick, and the pieces are attached together with finger pressure for several minutes in a back to back position, being careful not to touch the coated service. The samples are allowed to dry overnight before the measurements. Measurements are made using three liquids for certainty, one polar liquid (HPLC grade water), having a surface energy of 72.8 dynes/cm and one non polar liquid (99 ^* +-% Pure) hexadecane, from Aldrich Chemical) having a surface energy of 48.3 dynes/cm, are required; ethylene glycol (99.8%, from Aldrich Chemical) was used as the third liquid.

The sample is placed on a plate, and contacted with the liquid. The excess force resulting from surface tension is measured. Identical film samples are contacted with each ofthe liquids and the surface energy ofthe sample is calculated.

Examples

Example 1 and Comparative Examples C2 and C3 A single layer having the following underlayer composition was coated onto a primed polyester substrate, and after being dried for 2 minutes at 100°C. The nonionic surfactant and metal chelate containing top layer described below was then coated onto

the underlayer at 75 μm wet thickness and dried at 100°C for 1 min. This was Example 1.

A second sample ofthe underlayer composition was coated, pud then dried for 2 minutes at 100°C. This single layer recording sheet was Comparative Example C2. Finally, a third sample ofthe underlayer composition was overcoated with a top layer containing a metal chelate ofthe invention, i.e., triethanolamine titanate chelate, but no nonionic surfactant, at 75 μm wet thickness, and then dried in an oven at 120°C for 1 min. This was Example Cl.

The ink-recording sheets were then imaged on an Epson Color Stylus® Printer; in two tests, Example C2 had a black density of only 0.65, Example C3 had a black density of between 0.80 and 0.84, Example 1 had a black density of between 0.90 and 0.94.

As can be seen, the black density ofthe two layer coating system with metal chelate (but no nonionic surfactant) was improved over the single layer coating which does not contain either the metal titanate chelate or nonionic surfactant; however, the two-layer coating of Example 1 containing both the nonionic surfactant and the metal ion chelate exhibited a black denisty with was highly improved over both comparative examples.

The mordant disclosed below has the following structure:

wherein n is an integer of 2 or greater.

Underlayer Composition Black densitv

Example Cl

PVP/DMAEMA [Copolymer-958] (50%) 52% PVA Blend [Airvol-520 + Gohsehnol KPO-6] (12.2%) 34.7% Polyethylene glycol [Carbowax-600](50%) 7.8% Mordant P134 (20%) 3.8% 0.65

HydroxypropylmethylfMethocel® F-50] (4%) 1.4% Cross-linker XAMA-7 (16%) 0.33%

Top Layer Composition for Example 1 Black densitv

HPMC (3.5%) 63%

Titania-triethanolamine-complex [Tyzor® TE] (80%) 34% 0.94-0.90

Zonyl® FSO Surfactant (10%) 3%

Top Laver Composition for Example C2 Black densitv

Hydroxypropylmethylcellulose [HPMC] (3.5%) 65% Titania-triethanolamine-complex [Tyzor®TE] (80%) 35% 0.84-0.80

Examples 3-9 These examples show the variation of black density in the film in Example 1 with the variation of Zonyl® FSO fluorochemical surfactant levels. The films were imaged in an Epson Color Stylus® Printer and the densities were measured by densitometer under ambient conditions.

Example No. Zonvl® FSO (% wt) Black densitv

3 1.0 0.95-0.90

4 1.5 0.95-0.90

5 2.0 0.95-0.88

6 2.5 0.92-0.88

7 3.0 0.92-0.88

8 4.0 0.92-0.88

9 5.0 0.92-0.88 Example 10

The underlayer was coated as described in Example Cl, and a top layer containing a metal chelate ofthe invention, i.e., an aluminum triethanolamine chelate, and a nonionic surfactant was coated onto the underlayer in at 75 μm wet thickness at 120°C for 1 min.

Example 10 Black densitv

HPMC (3.5%) 63

Aluminum-triethanolamine complex (84%) 35 1.04-1.01

Zonyl® FSO Fluorochemical surfactant ( 10%) 2%

Examples 11-15 These examples show the variation of black density in the film of composition in example 10, with Zonyl® FSO fluorochemical surfactant levels.

Example No. Zonvl® FSO Surfactant f%wt Black densitv

11 0.5 1.01

12 1 1.02-1.00

13 2 1.01-1.00

14 3 1.00-0.98

15 4 1.00-0.99 Examples 16-19 These Examples have the same composition as Example 10, except that the

Zonyl® FSO was replaced with 3M fluorochemical surfactant, FC 170C. The following table shows the variation of black density when the surfactant level is varied. Films FC 170C (%wf) Black densitv

16 1 0.98-0.96

17 2 0.96-0.92

18 3 0.94-0.92

19 4 0.96-0.94

Examples C20 and C21

These examples show the affect of various fluorochemical surfactants used at 1%. This is a two layer system with the underlayer being identical to Example 1, except that Zonyl® FSA and Zonyl®FSJ are used as the surfactants. Both are anionic surfactants available from DuPont. Example 4, using a nonionic surfactant at 1% is provided as a comparison. As can be seen from the data, use ofthe anionic fluorochemical surfactants does not yield high black density values when compared to use ofthe nonionic fluorocarbon surfactants.

Ex. Nos. Type of Surfactant Surfactant Black Density wt%

4 Zonyl FSO-nonionic 1 0.95-0.90

C20 Zonyl FSJ-anionic 1 0.74-0.70

C21 Zonyl FSA-anionic 1 0.72-0.70

Examples 23-28 These examples show, in the composition in Example 10, the affect of various fluorochemical surfactants with different hydrophobic group on black density.

As can be seen, the anionic surfactants did not provide the increased black density. However, Zonyl®TM, a fluorocarbon methacrylate monomer having the structure

is nonionic surfactants; however, ink-recording sheets having this composition in the coating did not provide the improved black density values. It is believed that the surfactant does not contain enough hydrophilicity to draw the ink quickly into the coating, and improve the density.

Ex. Nos Tvpe of Surfactant Surfactant Black Densitv wt%

23 Zonyl® FSO-nonionic 1 1.02-1.00

24 Zonyl® FSA-anionic 1.5 0.80-0.78

25 Zonyl® FSA-anionic 5 0.80-0.75

26 Zonyl® TM-nonionic int. 1 0.82-0.80

27 Zonyl® TM-nonionic int. 5 0.82-0.78

28 Zonyl® 7950-anionic 5 0.84-0.81 Examples 29-31

These examples illustrate the affect of various fluorochemical surfactants which contain different hydrophilic portions on black density in the film of Example 1. These Fluorad® surfactants, available from 3M, are nonionic with the same fluorocarbon tail but different hydrophilic moieties.

Fluorad® FC-430, having the following structure:

R =

does not provide the density improvement. This is a very large molecule with very little fluorocarbon present to balance the large polymer. It is believed that this nonionic surfactant is not hydrophobic enough to bloom to the surface ofthe top layer, and that such blooming is further impeded by the size ofthe polymer.

Ex. Nos. Type of Surfactant Surfactant Black Density wt%

35 FC 170C 1 0.92-0.88

36 FC 171 1 0.94-0.90 37C FC 430 1 0.74-0.70

Example 38 and Comparative Examples C39-C45 The underlayer in each ofthe following examples was machine coated onto 100 μm polvinylidene chloride (PVDC) primed poly(ethylene terephthalate) to give a dry coat weight of 9.7 g/m ² . The coating comprises 29.6% polyvmylalcohol, available as Airvol® 523 from Air Products, 5.2% of a polyvmylalcohol having a different hydrolysis number, available as Gohensol® KP06 from Nippon Synthetic Chemical, 52.2% of a copolymer of poly(vinylpyrrolidone)/dimethylaminoethylmethacrylate, available as "Copolymer 958" from GAF, and 10% polyethylene glycol, available as Carbowax® 600 from Union Carbide. The top coat for each example contained 10% Tyzor® TE, a triethanolamine titanate chelate, and 10% poly(methylmethacrylate) beads as well as the varying ingredients described in the following table for complete 100%. Each ofthe examples was knife coated 75 μm thick wet atop the underlayer, and dried at about 95 °C for 2 minutes. This gives a dry coating weight of 0.08-.10 g/m ² . The films were then evaluated by imaging a solid fill black rectangle on the

Epson Stylus Printer® using the transparency print mode. The optical density of each image is then measured.

Methocel Zonyl FSO Zonyl UR Zonyl FSJ

Example F50 wt% wt% wt% O.D.

No. wt%

C39 80 0.72

38 77 3 0.92

C40 79 1 0.64

C41 77 3 0.63

C42 75 5 0.62

C43 79 1 0.64

C44 77 3 0.66

C45 75 5 0.65

As can be seen from the data, the fluorocarbon of example 38, the only nonionic fluorocarbon surfactant provides superior optical density and the anionic surfactants employed in Comparative Examples C39-C45 do not.

Wilhelmy balance measurements were also completed for Example 38 and Comparative Examples C39-C45. As the following table shows, the nonionic fluorocarbon surfactant has the highest surface energy with the two anionic surfactants at all three different concentrations having much lower surface energies.

Example No. Surfactant Total surface energv

(dynes/cm)

38 3% Zonyl FSO (3410) 38.0

C39 no surfactant 31.9

C40 1% Zonyl® FSJ 17.5

C41 3% Zonyl® FSJ 16.5

C42 5% Zonyl® FSJ 18.5

C43 1% Zonyl® UR 19.8

C44 3% Zonyl® UR 14.9

C45 5% Zonyl® UR 17.9 Example 46 An ink-jet recording sheet was made as follows. The substrate provided was a

100 μm white microvoided polyester having an opacity of 90%. A two layer ink-jet coating system was coated thereon. The underlayer contained 29.6% polyvinyl alcohol as Airvol 523, 5.2% polyvinyl alcohol as Gohesnol KPO6, 52.2% of a copolymer of PVP/DMAEMA as "Copolymer 958", and 10% polyethylene glycol as Carbowax® 600, and 3% of a mordant, having the structure disclosed in Example 1, supra. This layer was machine coated to give a dry coating weight of about 9.7 g m ² .

The top layer contained 77% Methocel F50, 10% Tyzor TE, 10% PMMA beads, and 3% Zonyl FSO. This layer was machine coated to give a dry coating weight of 0.81 g m ² . The ink-jet recording sheet was dried at 121°C for 1 minute. When imaged on the Epson Stylus® Printer using the media setting for special coated paper, and the microweave print option, the images were of excellent quality at both 360 dpi and 720 dpi resolution.

Example 47 An ink-jet recording sheet was made as follows. The substrate provided was PVDC primed polyester film. A two-layer coating system was coated thereon. The underlayer contained 34% PVA blend, 52% Copolymer 958, and 7.8% Carbowax® 600, 1.4% Methocel F50, and 3.8% P134 mordant, having the structure disclosed in Example 1. This layer was machine coated to give a dry coating weight of about 9.7 g/m ² .

The top layer was coated wet in 50 μm thickness, and contained 41% hydroxypropylmethyl cellulose (Methocel F50), 39% acetyl acetonate (Tyzor GBA), 7.2% polyethylene glycol (Carbowax® 8000), 10% poly(methylmethacrylate) (PMMA) beads, and 3% Zonyl® FSO. The ink-jet recording sheet was dried at 121°C for 1 minute.

When imaged on the Epson Stylus® Printer, the density was 0.92.

Example 48 The underlayer was coated as described in Example Cl, and a top layer containing 34% zirconium triethanolamine chelate, 65% hydroxypropylmethylcellulose and 1% Zonyl® FSO, was coated onto the underlayer in at 75 μm wet thickness at 120°C for 1 min. The Black density was between 0.91 and 0.93.