FIELD OF THE INVENTION The present invention relates to inkjet printing, and in particular to a specific ink set with combinations of light and dark dye load of a given color for improving inkjet image quality.

BACKGROUND OF THE INVENTION Color inkjet printers typically use three inks of differing hue: magenta, yellow, and cyan, and optionally black. The particular set of colorants, e. g. , dyes, used to make the inks is called a"primary dye set. "A spectrum of colors, e. g., secondary colors, can be generated using different combinations of the primary dye set.

A successful ink set for color inkjet printing must be compatible with the inkjet pen and printing system. Some of the required properties for the inkjet ink include: good crusting resistance, good stability, the proper viscosity, the proper surface tension, little color-to-color bleed, rapid dry time, no negative reaction with the vehicle, high solubility of the dyes in the vehicle, consumer safety, low strike through, high color saturation, and good dot gain.

Furthermore, the colored characteristics of the colorants play an important role in the quality of the printed inkjet image. Up to the present time, color inkjet inks have been designed and tailored for printing business graphics such as depiction of information in the form of"pie-charts"and"bar-charts"on plain paper. These applications require that inkjet use bright, vivid, high chroma colorants that, in general, are neither lightfast nor resistant to air fade.

One attribute that is particularly important in imaging (i. e., color rendition of pictures) is"grain". Grain describes how visible the dots are to the viewer. If large, dark drops are used, the dots become very visible and image quality is degraded.

One technique to reduce grain is to use smaller drop weight to produce nearly invisible drops. The down side to this technique is the need for more difficult and more costly manufacturing processes due to the requirement for smaller orifice holes and resistors and more difficult reliability challenges due to the smaller holes.

Another technique is to use additional"light"inks such as a light magenta or cyan at colorant ladings 5-25% of the normal or dark ink. This technique allows the use of larger, low colorant load drops. These"light"drops are less visible due to the presence of less colorant. One downside to this approach is that these"light"inks fade much faster on media than the dark inks. This fade often occurs in critical areas such as the skin tone in a picture of a human being.

Thus, there is a need for more lightfast and air fade resistant colorants to be used in these light inks.

SUMMARY OF THE INVENTION The present invention relates to an ink set for ink-jet printing, wherein at least one ink of the ink set comprises a light dye load and a dark dye load, both the light dye load and the dark dye load being one color, the one color being selected from the group consisting of magenta, cyan, yellow and black ;

and the light dye load being at least one of air fade resistant, light fade resistant and humid color migration resistant.

The present invention also relates to a method for inkjet printing, the method comprising the step of ejecting ink from an inkjet, the ink comprising a light dye load and a dark dye load, both the light dye load and the dark dye load being one color, the one color being selected from the group consisting of magenta, cyan, yellow and black ; and the light dye load being at least one of air fade resistant, light fade resistant and humid color migration resistant.

BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 gives a graphical representation of air fade in two inkjet printing systems by graphing the time to reach 25% Optical Density loss in days vs. initial optical density of the printed image for the two inkjet printing systems, one having both light and dark magenta dyes in the ink and one having just dark magenta dye in the ink.

DETAILED DESCRIPTION OF EMBODIMENTS OF THE INVENTION Inkjet printers are increasingly moving to a multi-dye-load configuration in which lighter colors are printed using light dye load dye inks and darker colors are printed using dark dye load dye inks. Such multi-dye-load inkjet printer configurations can however have problems because the light dye load inks fade much faster. The present application describes a multi-dye-load configuration in an inkjet printer having at least one dye of the set of cyan, magenta, yellow or black which is at least one of air fade resistant, light fade resistant, and humid color migration resistant. This dye is used in a light dye load ink in the multi- dyeload configuration along with a dark dye load ink of the same color.

Using a light ink in the multi-dyeload configuration is desirable because it allows the use of low dye loads. However, even though low dye loads reduce dot

visibility and grain in photo prints, thus increasing photo quality, these same low dye loads are particularly susceptible to air fade. Accordingly, the applicants have found a way by using a combination of light dye load dye with good air fade resistance and dark dye load dye to deliver exceptional photo Image Quality (IQ) and images that are resistant to fade.

Previous ways of dealing with this problem have used a single set of dye loads or have used a light dye load that was resistant to light fade but not air fade.

The present application describes a set of inkjet inks having at least one dye of the set cyan, magenta, yellow, or black which is used as a light dyeload in a multi-dyeload printer and is at least one of air fade resistant, light resistant, and humid color migration resistant.

Non-limiting examples of the magenta dye are: anthrapyridone, H-acid (azo: H- acid), gamma acid (azo: y-acid), xanthene types, polyvalent metal coordinated dyes (azo: Cu or Ni), or mixtures thereof.

An example of an anthrapyridone is: C. I. Acid Red 81 (manufactured by Bayer AG, Leverkeusen, Germany). A generic dye structure of an anthrapyridone is given below : Examples of H-acids (Azo: H-acids) are: Reactive Red 180 (RR180) (manufactured by Avecia Limited, Manchester, UK), Reactive Red 31 (RR31) (manufactured by Avecia Limited, Manchester, UK). A generic dye structure of an H-acid is given below :

An example of a gamma acid is Magenta 377 (M377) (the same dye disclosed in U. S. Patent No. U. S. 6,423, 375 incorporated herein by reference, manufactured by 9ford Imaging GmbH, Marly, Switzerland). A generic dye structure of a y-acid is given below.

Examples of xanthene dyes are: Acid Red 52 (AR52) (manufactured by Avecia Limited, Manchester, UK) and Acid Red 289 (AR289) (manufactured by Avecia Limited, Manchester, UK).

A generic structure of a xanthene dye is given below :

where non-limiting examples of X+ can be O, OH+, N (R2) +, N (H2) +, etc.

Examples of polyvalent metal coordinated dyes are pyridyl azo quinolines and the closely related pyridyl azo naphthols.

A specific example of a pyridyl azo quinone (PAQ) is an 8-heterocyclylazo-5- hydroxyquinoline, already described in the parent application, 09/599,352, having a structure wherein: M represents a polyvalent transition metal ion selected from the group consisting of iron, nickel, copper, cobalt, zinc, and chromium; each L independently represents a neutral or anionic ligand ; each X, Y and Z independently represents a substituted or unsubstituted alkyl group of 1-6 carbon atoms, a substituted or unsubstituted aryl group of 6-10 carbon atoms, a substituted or unsubstituted hetaryl group of 5-10 atoms, a halogen, a cyano group, a nitro group, a substituted or unsubstituted alkoxycarbonyl group of 1-6 carbon atoms, a substituted or unsubstituted alkoxy group of 1-6 carbon atoms, a hydroxy group, a polyoxyalkylene group of 2-20 alkylen oxide residues, a carboxy group or a salt thereof, a sulfo group or a salt thereof, a phospho group or a salt thereof, a carbamoyl group, a substituted or unsubstituted alkyl-, aralkyl-, aryl-, diaryl-or dialkyl-carbamoyl group of 1-20 carbon atoms, a sulfamoyl group, a substituted or unsubstituted alkyl-, aralkyl-,

aryl-, diaryl-or dialkyl-amino group of 1-20 carbon atoms or a quaternary ammonium or phosphonium group; Q represents the atoms necessary to complete a 5-or 6-membered heterocyclic ring; n represents 2 or 3; m represents an integer from 1-3; each p and r independently represents an integer from 0-3; q represents 0,1 or 2 two or more of L may be joined together to form a bi-or tridentate ligand which may optionally comprise another polydentate molecule of the same or different structure as shown above; one or more of L may be combined with X and/or Z; one or more of X, Y and Z, together with the carbon to which they are attached, may independently represent a ring nitrogen; and any two of X, Y or Z may be joined together to form a 5-7 membered saturated or unsaturated ring.

Another specific example of pyridyl azo quinone (PAQ) is Reactive Red 23 (RR23) (Avecia Limited, Manchester, UK).

Yet another specific example is the magenta dye having the structure: wherein M is H or a monovalent ion, such as Na+, Li+, K+, NH4+, and combinations thereof (disclosed in Application Serial Number 10/094,911 filed March 11,2002).

A generic structure of the polyvalent metal coordinated dye, covering either

pyridyl azo quinone (PAQ) or pyridyl azo naphthol is where M is a polyvalent transition metal ion selected from the group consisting of iron, nickel, copper, cobalt, zinc, and chromium.

Non-limiting examples of cyan dyes that have at least one of air fade resistance, light fade resistance and humid color migration resistance are copper phthalocyanine dyes such as the related dyes cyan 485 and cyan 485/4, both having the structure copper, (29H, 31 H-phthalocyaninato (2-) - xN29, xN30, xN31, xN32) aminosulfonyl ((2-hydroxy-ethyl) amino) sulfonyl sulfo derivatives, sodium salt.

Non-limiting examples of yellow dyes that have at least one of air fade resistance, light fade resistance and humid color migration resistance are monoazo yellow dyes and bisazo yellow dyes such as Yellow 1189 having the structure 1, 3-naphthalenedisulphonic acid, 7- ( (4- ( (4, 6-bis- ( (3-sulfoprop-1- yl) thiol (-1,3, 5-triazin-2-yl) amino (-3-methoxyphenyl) azo) tetrasodium salt.

Copper: Azo black dyes have also been found to have at least one of air fade resistance, light fade resistance and humid color migration resistance.

In another non-limiting embodiment, the dyes of the dark dye load are the same as the dyes in the light dye load.

In another non-limiting embodiment of the invention, at least one of the dyes in the dark dye load is different from the dyes used in the light dye load of the given color.

In another non-limiting embodiment, all of the dyes of the dark dye load are different from all of the dyes of the light dye load.

In yet another non-limiting embodiment, the dyes used in the dark inks are at least one of light fade resistant, air fade resistant and humid color migration resistant.

EXAMPLES Example 1-Twenty two different magenta dyes were tested for humid shift as follows. Each magenta dye was applied to three different types of inkjet printable media: Media 1 (swellable), Media 2 (porous, Al203 coated) and Media 3 (porous, Si02 coated). Each dye was therefore tested on three different media samples. Each sample tested was exposed to 35°C/80% Relative Humidity (RH) for 4 days. Table 1 lists the humid hue shift (HF) of each sample measured in terms of hE (Average AE CIE94). When used to measure humidfastness, this value is a measure of the color difference or color shift after exposure to high humidity (4 days @ 35°C, 80% RH) and is calculated as follows : hE= [(AL*) 2+ (/\a*) 2+ (Ab*) 2] 0 5. The L*a*b* values are measured before and after exposure to the humid conditions. In this system, L* defines the lightness of a color ranging from 0 (black) to 100 (white). a* and b* together define the hue, with a* ranging from a negative number (green) to a positive number (red), and b*ranging from a negative number (blue) to a positive number (yellow). The average AE value is simply the average of all AE values (in other words, an average of color shift values from low to high print densities).

On Table 1 below, dyes are sorted by hE collective performance on all three media. Pyridyl azo naphthol (PAN) dyes were found to be the most humidfast.

As shown, H-acids and y-acids are moderately humidfast. Xanthenes, pyridyl azo quinone (PAQ) dyes and anthrapyridones are the least humidfast. H-acids tend to fail on porous Si02 coated media such as Media 3. y-acids tend to fail on swellable media such as Media 1. For use in this example, besides the dyes specifically mentioned in the Detailed Description section above, other related dyes are used which fall in the categories of H-acids, y-acids, xanthenes, polyvalent metal coordinated dyes, and anthrapyridones. They include: Magenta Dye 1 (nickel : pyridyl azo naphthol) ; Magenta Dye 2 (nickel : pyridyl azo naphthol) ; Magenta Dye 3 (copper: pyridyl azo naphthol) ; Magenta Dye 4 (azo: H-acid); Magenta Dye 5 (azo: y-acid) ; Magenta Dye 6 (copper: pyridyl azo naphthol) ; Magenta Dye 7 (azo: H-acid); Magenta Dye 8 (Ni: naphthol azo imidazole) ; Magenta Dye 9 (azo: y-acid) ; Magenta Dye 10 (azo: H-acid); Magenta Dye 11 (azo: H-acid); Magenta Dye 12 (azo: y-acid) ; Magenta Dye 13 (nickel : pyridyl azo quinone) ; and Magenta Dye 14 (anthrapyridone).

Table 1 Dye Structure Media 1 Media 2 Media 3 Magenta Dye 1 Ni: pyridyl azo naphthol 2.4 1. 3 0. 8 Magenta Dye 2 Ni: pyridyl azo naphthol 2.4 1.0 1.3 Magenta Dye 3 Cu 1. 3 1. 5 2. 3 Magenta Dye 4 H-acid 1. 8 1. 7 1. 8 Acid Red 249 azo 1. 2 0. 8 2. 2 Magenta Dye 5 y-acid 1. 5 2. 3 2. 7 Magenta Dye 6 Copper azo 2. 2 2. 4 3. 1 Magenta Dye 7 H-acid 1. 8 1. 9 3. 3 Magenta Dye 8 Ni: naphthol azo imidazole (struc- 3. 1 2.7 1.8 ture disclosed in W00148090 and 10/094911) Reactive Red H-acid 2. 5 2. 6 3. 8 180 (RR180) Magenta Dye 9 y-acid 4. 1 2. 8 1. 1 Magenta Dye H-acid 2. 4 2. 2 3. 6 10 Magenta Dye H-acid 3. 2 2. 9 4. 1 11 M377 (disclosed y-acid 4.4 3.2 1. 0 in 6,423, 375) Magenta Dye y-acid 5. 0 3. 0 2. 9 12 Reactive Red H-acid 2. 1 1. 9 6. 5 31 (RR31) Reactive Red Cu : azo 3.3 5.0 4.7 23 (RR23) Magenta Dye Ni: pyridyl azo quinone 2.0 4.5 8.6 13 Acid Red 52 xanthene 3. 0 6.9 6.1 (AR52) Acid Red 289 xanthene 1. 7 4. 2 4. 9 (AR289) C. i. Acid Red 81 anthra-pyridone 5. 8 5. 2 2. 0 Magenta Dye anthra-pyridone 4.0 4.2 4.5 14

Example 2- Twenty three different magenta dyes were tested for airfade as follows. Each magenta dye was applied to two different types of inkjet printable media: Media 2 (porous, Al203 coated) and Media 3 (porous, Si02 coated). Each dye was therefore tested on two different media samples. Each sample was submitted to a 48 day dark forced air fade (30-50% Relative Humidity, 23-25°C). The dyes are listed in Table 2 in order of performance on Media 3, an Si02 coated media.

The tests showed that H-acids and anthrapyridones are airfast. PAN dyes are moderately airfast. y-acids and PAQ dyes are not airfast. Media 2, porous coated with Al203, is less airfast relative to those on Media 3 which is Si02 coated. No airfade is observed on Media 1 which is swellable media.

Furthermore it has been observed that only y-acids exhibit air fade on plain paper. For use in this example, besides the dyes specifically mentioned in the Detailed Description section above, other related dyes are used, all of which are also used in Example 1, which fall in the categories of H-acids, y-acids, xanthenes, polyvalent metal coordinated dyes, and anthrapyridones. They include : Magenta Dye 1 (Ni: pyridyl azo naphthol) ; Magenta Dye 2 (nickel : pyridyl azo naphthol) ; Magenta Dye 3 (copper: pyridyl azo naphthol) ; Magenta Dye 4 (azo: H-acid); Magenta Dye 6 (cooper: pyridyl azo naphthol) ; Magenta Dye 7 (azo: H-acid); Magenta Dye 8 (nickel : naphthol azo imidazole) ; Magenta Dye 9 (azo: y-acid) ; Magenta Dye 10 (azo: H-acid); Magenta Dye 11 (azo: H-acid); Magenta Dye 12 (azo: y-acid) ; Magenta Dye 13 (nickel : pyridyl azo quinone) ; Magenta Dye 14 (anthrapyridone); Magenta Dye 15 (azo).

Table 2 % OD Loss Dye Structure Media 2 Media3 Magenta Dye 4 H-acid 4% 0% Magenta Dye 3 Cu 2% 1 % Magenta Dye 14 anthrapyridone 2% 1% Magenta Dye 7 H-acid 3% 2% Magenta Dye 11 H-acid 5% 2% Magenta Dye 15 azo 4% 2% Reactive Red 31 H-acid 4% 2% (RR31) Magenta Dye 6 Copper azo 4% 3% Reactive Red 180 H-acid 3% 3% (RR180) Magenta Dye 10 H-acid 3% 4% Acid Red 289 xanthene 2% 4% (AR289) C. I. Acid Red 81 anthrapyridone 4% 4% Acid Red 249 azo 7% 4% Reactive Red 23 Cu : azo 5% 5% (RR23) Magenta Dye 1 Ni: pyridyl azo naphthol 9% 8% MagentaDue 2 Ni : pyridyl azo naphthol 10% 9% Acid Red 52 (AR52) xanthene 17% 13% M377 (disclosed in y-acid 36% 14% 6,423, 375) Magenta Dye 8 Ni : naphthol azo imidazole 25% 17% (structure disclosed in W00148090 and 10/094911) Magenta Dye 5 y-acid 46% 25% Magenta Dye 9 y-acid 60% 35% Magenta Dye 12 y-acid 64% 45% Magenta Dye 13 Ni-pyridyl azo quinone 78% 47%

Example 3- Twenty three different magenta dyes were tested for lightfade as follows. Each magenta dye was applied to four different types of inkjet printable media samples : Media 1 (swellable), Media 2 (porous, A1203 coated), Media 4 (porous, Si02 coated, different bore than Media 3) and Media 5 (plain paper, cellulose based). Years to failure were estimated using a 19 year simulated light fade process under glass. The dyes were sorted in Table 3 in order of the light fade performance of the dyes on Media 4 (porous, Si02 coated). It was found that dyes on Media 1 (swellable) were more lightfast relative to the same dyes on other media. Metalized dyes and y-acids were the most lightfast. Xanthenes, H-acids, and anthrapyridones were comparatively not lightfast. y-acid dyes were found to be more lightfast on Media 4 (porous, Si02 coated) than Media 2 (porous, Al203 coated) presumably because of the different bore size of the Al203 coating. For use in this example, besides the dyes specifically mentioned in the Detailed Description section above, other related dyes, most of which mentioned in Examples 1 and 2, are used which fall in the categories of H-acids, y-acids, xanthenes, polyvalent metal coordinated dyes, and anthrapyridones.

They include : Magenta Dye 1 (nickel : pyridyl azo naphthol) ; Magenta Dye 2 (nickel : pyridyl azo naphthol) ; Magenta Dye 3 (copper: pyridyl azo naphthol) ; Magenta Dye 4 (azo: H-acid); Magenta Dye 5 (azo: y-acid) ; Magenta Dye 6 (cooper: pyridyl azo naphthol) ; Magenta Dye 7 (azo: H-acid); Magenta Dye 8 (Ni: naphthol azo imidazole) ; Magenta Dye 9 (azo: y-acid) ; Magenta Dye 10 (azo: H-acid); Magenta Dye 11 (azo: H-acid); Magenta Dye 12 (azo: y-acid) ; Magenta Dye 13 (nickel : pyridyl azo quinone) ; Magenta Dye 14 (anthrapyridone); and Magenta Dye 15 (azo).

Table 3 Years to failure under glass Dye Structure Media 1 Media 2 Media 4 Media 5 Reactive Red 23 (RR23) Cu: azo 30+ 30+ 30+ 30+ Magenta Dye 3 Cu: naphthol azo 30+ 30+ 30+ 30+ imidazole Magenta Dye 8 (structure Ni: naphthol azo 30+ 30+ 30+ 30+ disclosed in W00148090 and imidazole 10/094911) Magenta Dye 9 y-acid 30+ 23.2 30+ 26.4 M377 (disclosed in 6,423, 375) y-acid 30+ 16. 3 30+ 24. 1 Magenta Dye 1 Ni : pyridyl azo 30+ 18. 3 28. 1 26. 0 naphthol Magenta Dye 12 y-acid 30+ 14. 1 24. 5 13. 5 Magenta Dye 2 Ni : pyridyl azo 30+ 12. 9 21. 0 18. 7 naphthol Magenta Dye 5 γ-acid 30+ 9.9 18.7 13.6 Magenta Dye 10 H-acid 19. 9 15. 6 15. 6 6. 3 Magenta Dye 13 Ni-pyridyl azo 30+ 16. 4 12. 9 30+ quinone Magenta Dye 6 Copper azo 29.4 10.0 10.3 15.5 Magenta Dye 14 anthrapyridone 14.9 14.4 7.0 8.9 Magenta Dye 7 H-acid 12. 8 8. 9 5. 8 3. 0 Reactive Red 180 (RR180) H-acid 10. 5 6. 2 5. 5 3. 3 Magenta Dye 11 H-acid 11. 3 7. 0 3. 4 2. 7 C. l. Acid Red 81 anthrapyridone 5.3 4.4 3.4 6.5 Acid Red 249 azo 11. 8 5. 5 2. 6 3. 1 Reactive Red 31 (RR31) H-acid 6. 5 3. 3 2. 5 2. 4 Magenta Dye 15 azo 12. 0 4. 1 2. 4 10. 0 Magenta Dye 4 H-acid 14. 8 7. 2 1. 9 3. 8 Acid Red 289 (AR289) xanthene 2. 3 1. 7 1. 8 2. 0 Acid Red 52 (AR52) xanthene 1. 1 1. 2 1. 1 1. 1

Example 4- Of the inks tested in Examples 1,2 and 3, some were applied in a light load and some were applied in a dark load. In Table 4, the results of some light load and dark load magenta samples were compared. Magenta Dye 4, Magenta Dye 10 and C. I. Acid Red 81 dyes were each applied in a dark magenta load to Media 4. By the same token, Magenta Dye 3 and Magenta Dye 1 were each applied in a light magenta load to Media 4. The results are shown in Table 4. For use in this example, besides the dyes specifically mentioned in the Detailed Description section above, other related dyes already mentioned in Examples 1, 2 and 3, are used which fall in the categories of H-acids, y-acids, xanthenes, polyvalent metal coordinated dyes, and anthrapyridones. They include: Magenta Dye 1 (nickel : pyridyl azo naphthol) ; Magenta Dye 3 (copper: pyridyl azo naphthol) ; Magenta Dye 4 (azo: H-acid); Magenta Dye 10 (azo: H-acid).

Table 4 Dyes Humidfastness Air Fade (48 LF glass day test) Dark Magenta Dye 4 1.8 # 0% 1.9y Magenta Load Magenta Dye 10 3. 6 DE 4% 15.6y C. l. Acid Red 81 2. 0 #E 4% 3.4y Light Magenta Dye 3 2. 3 hE 1% 30+y Magenta Load Magenta Dye 1 0. 8 Axe 8% 26y

Example 5- Two inkjet printing systems, a system with both light and dark magenta inks and a system with just dark magenta ink, were used to plot the relationship between the time to reach 25% Optical Density Loss in a 200 day dark forced air fade (30-5-% Relative Humidity, 23-25°C) in the printed ink images printed by the two systems and the initial optical density of the printed ink images, thus showing comparative air fade in the two systems. Figure 1 plots the relationship on a graph. The graph shows a dramatic difference between the images printed with the system having both light and dark magenta ink and the system having just dark magenta ink. The first system with the light and dark inks takes a much longer time to reach 25% Optical Density Loss than the second system. Initially the first system prints with just the light magenta ink and gradually more dark ink is added. The time for 25% optical density loss drops precipitously as the initial optical density increases due to the dark ink coming to constitute a larger and larger part of the ink mixture. In contrast, the time for 25% optical loss remains essentially the same for the second system having just the dark ink because as the initial optical density increases the proportion of dark ink does not increase in the second system, but remains the same, 100%. The time to reach 25% optical density in both systems is a good indicator of relative airfastness.

Example 6- Eight different yellow dyes were tested for airfade as follows. Each yellow dye was applied to three different types of inkjet printable media: Media 6 (porous Al203 coated); Media 4 (porous Si02 coated); Media 7 (porous Si02 coated).

Each dye was therefore tested on three different media samples. Each sample was submitted to a 57 day dark forced air fade (30-50% Relative Humidity, 23- 25°C). The dyes are listed in Table 6 in order of performance on Media 6, Media 4 and Media 7. The tests showed that azo and disazo yellow dyes are airfast, with Yellow Dye 3 being less airfast than the other dyes on all three of the media tested. For use in this example, besides the Y1189 dye specifically mentioned in the Detailed Description section above, other related dyes are used which fall in the categories of azo and disazo yellow dyes. They include: Yellow Dye 1 (azo); Yellow Dye 2 (disazo); Yellow Dye 3 (azo); Yellow Dye 4 (azo); Yellow Dye 5 (disazo); Yellow Dye 6 (azo); Yellow Dye 7 (azo).

Table 6 Acc. Air Fade (Days to Fail (57 days)) Dye Structure Media 6 Media 4 Media 7 (porous Al203 (porous Si02 (porous Si02 coated) coated) coated) Yellow Dye 1 azo 570+ 570+ 570+ Y1189 azo 570+ 570+ 570+ Yellow Dye 2 disazo 570+ 570+ 404 Yellow Dye 3 azo 293 405 244 Yellow Dye 4 azo 570+ 570+ 570+ Yellow Dye 5 disazo 570+ 570+ 570+ Yellow Dye 6 azo 570+ 570+ 570+ Yellow Dye 7 azo 312 570+ 362 Example 7- The eight yellow dyes of Example 6 were tested for lightfade as follows. Each yellow dye was applied to inkjet printable media: Media 1 (swellable) both bare and under glass. Years to failure were estimated using a 21 year simulated light fade process under glass. Yellow dye 1, Y1189, Yellow dye 2 and Yellow dye 3 were found to be equally lightfast and better than Yellow dye 4, Yellow dye 5, Yellow dye 6 and Yellow dye 7.

Table 7 Acc. Light Fade (Days to Fail (21 years) ) Dye Structure Media 1, bare Media 1, glass Yellow Dye 1 azo 87 158 Y1189 azo 49 96 Yellow Dye 2 disazo 38 124 Yellow Dye 3 azo 33 72 Yellow Dye 4 azo 27 50 Yellow Dye 5 disazo 26 53 Yellow Dye 6 azo 25 46 Yellow Dye 7 azo 22 49

Example 8- Five different cyan dyes were tested for airfade as follows. Each cyan dye was applied to two different types of inkjet printable media: Media 2 (porous Al203 coated); Media 3 (porous Si02 coated). Each dye was therefore tested on two different media samples. Each sample was submitted to a 69 day dark forced air fade (30-50% Relative Humidity, 23-25°C). The dyes are listed in Table 8 in order of performance on Media 2and Media 3. For use in this example, besides 485/4 and 485 dyes specifically mentioned in the Detailed Description section above, other related dyes are used all of which fall in the category of copper phthalocyanine cyan dyes. They include : Cyan Dye 1 (copper phthalocyanine) ; Cyan Dye 2 (copper phthalocyanine) ; and Cyan Dye 3 (copper phthalocyanine) Table 8 % OD Loss after 69 days Dye Media 2 (porous Al203 Media 3 (porous Si02 coated) coated) Cyan Dye 1 3 6 485/4 13 8 Cyan Dye 2 10 11 485 29 16 Cyan Dye 3 41 20

Example 9- The five cyan dyes of Example 9 were tested for lightfade as follows. Each cyan dye was applied to inkjet printable media: Media 2 (porous Al203 coated); Media 4 (porous Si02 coated); Media 5 (Cellulose plain paper); and Media 1 (swellable) both bare and under glass. Years to failure were estimated using a 20 year simulated light fade process under glass. As in example 8 above, besides 485/4 and 485 dyes specifically mentioned in the Detailed Description section above, other related dyes are used all of which fall in the category of copper phthalocyanine cyan dyes. They include: Cyan Dye 1 (copper phthalocyanine) ; Cyan Dye 2 (copper phthalocyanine) ; and Cyan Dye 3 (copper phthalocyanine).

Table 9 Acc. Light Fade, Years to Fail (20 yrs, ODo=0.5) Media 2 Media 4 (porous Media 5 Media 1 (porous Al203 Si02 coated) (Cellulose plain (swellable) coated) paper) Dye bare glass bare glass bare glass bare glass Cyan 50+ 50+ 50+ 50+ 50+ 50+ 50+ 50+ Dye 1 Cyan 22 50+ 19 50+ 50+ 50+ 50+ 50+ Dye 2 485/4 12 50+ 19 50+ 50+ 50+ 50+ 50+ Cyan 5 34 12 50+ 49 50+ 43 50+ Dye 3 485 6 36 13 50+ 45 50+ 33 50+

Example 10- A black dye, Black Dye 1, (copper: azo), was tested for airfade as follows. The black dye was applied to two different types of inkjet printable media: Media 2 (porous Al203 coated) and Media 3 (porous Si02 coated). The dye was therefore tested on two different media samples. Each sample was submitted to a 69 day dark forced air fade (30-50% Relative Humidity, 23-25°C).

Table 10 % OD Loss Dye Media 2, (porous Al203 Media 3 (porous, Si02 coated) coated) Black Dye 1 39 23

Example 11- The copper: azo black dye, Black Dye 1, of Example 10 was tested for lightfade as follows. The dye was applied to inkjet printable media: Media 2 (porous Al203 coated); Media 4 (porous Si02 coated); Media 5 (Cellulose plain paper); and Media 1 (swellable) both bare and under glass. Years to failure were estimated using a 20 year simulated light fade process under glass.

Table 11 Acc. Light Fade, Years to Fail (20 yrs, ODn=0. 5) Media 2, Media 4 Media 5 (plain Media 1 (porous Al203 (porous, Si02 paper, cellulose (swellable coated) coated) based) media) Dye Bare Glass Bare Glass Bare Glass Bare Glass Black 4 27 8 nf 50+ 50+ 50+ 50+ Dye 1)

What is Claimed is: