Europäisches Patentamt

(19) European Patent Office *EP001149879A2*

Office européen des brevets (11) EP 1 149 879 A2
(12) EUROPEAN PATENT APPLICATION

(43) Date of publication: (51) Int Cl.7: C09D 11/00

31.10.2001 Bulletin 2001/44

(21) Application number: 01303530.8

(22) Date of filing: 18.04.2001

(84) Designated Contracting States: (72) Inventor: Kabalnov, Alexey S.

AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU Corvallis, OR 97330 (US)
MC NL PT SE TR
Designated Extension States: (74) Representative: Colgan, Stephen James et al
AL LT LV MK RO SI CARPMAELS & RANSFORD
43 Bloomsbury Square
(30) Priority: 19.04.2000 US 552145 London WC1A 2RA (GB)

(71) Applicant: Hewlett-Packard Company

Palo Alto, CA 94304 (US)

(54) Microemulsion techniques for ink jet inks

(57) Aqueous inkjet inks with oil-soluble dyes that ing a microemulsion in the ink of solvent moieties with
are made more soluble in the aqueous vehicle by mak- both solubilizing groups and hydrophobic groups.
EP 1 149 879 A2

Printed by Jouve, 75001 PARIS (FR)

 EP 1 149 879 A2

Description

FIELD OF INVENTION

5 [0001] The invention relates to aqueous inkjet inks with oil-soluble dyes that are made more soluble in the aqueous
vehicle by making a microemulsion in the ink of solvent moieties with both solubilizing groups and hydrophobic groups.

BACKGROUND OF INVENTION

10 [0002] The use of inkjet printing systems has grown dramatically in recent years. This growth may be attributed to
substantial improvements in print resolution and overall print quality coupled with appreciable reduction in cost. Today's
inkjet printers offer acceptable print quality for many commercial, business, and household applications at costs fully
an order of magnitude lower than comparable products available just a few years ago. Notwithstanding their recent
success, intensive research and development efforts continue toward improving inkjet print quality, while further low-
15 ering cost to the consumer.
[0003] An inkjet image is formed when a precise pattern of dots is ejected from a drop-generating device known as
a "printhead" onto a printing medium. The typical inkjet printhead has an array of precisely formed nozzles located on
a nozzle plate and attached to an inkjet printhead substrate. The substrate incorporates an array of firing chambers
that receive liquid ink (colorants dissolved or dispersed in a solvent) through fluid communication with one or more ink
20 reservoirs. Each chamber has a thin-film resistor, known as a "firing resistor," located opposite the nozzle so ink can
collect between the firing resistor and the nozzle. In particular, each resistor element, which is typically a pad of a
resistive material, measures about 35 µm x 35µm. The printhead is held and protected by an outer packaging referred
to as a print cartridge, i.e., inkjet pen.
[0004] Upon energizing of a particular resistor element, a droplet of ink is expelled through the nozzle toward the
25 print medium, whether paper, transparent film or the like. The firing of ink droplets is typically under the control of a
microprocessor, the signals of which are conveyed by electrical traces to the resistor elements, thereby forming alpha-
numeric and other characters on the print medium.
[0005] Water is the most attractive solvent for inkjet ink. Because of this, drop-on-demand inkjet inks are 50-90%
water. Accordingly, most of the inkjet ink formulations are based on water-soluble colorants, that is, water-soluble dyes
30 or water-dispersible pigments. This comes at the price that inkjet images are not stable to water, in particular, to the
action of water combined with rubbing (so-called wet smudge).
[0006] On the other hand, there are many inks in the art that are stable to the action of water. These inks are based
on organic solvents and use solvent-soluble dyes or solvent-dispersible pigments. These inks are widely used in such
areas as continuous inkjet and gravure printing inks. The solvent systems used in these applications are methylethyl-
35 ketone, methylbutylketone, acetone, toluene, ethyl acetate, as well as solvent mixtures, such as 40% ethyl acetate,
40% ethyl alcohol, and 20% toluene. These solvents however are hard to use in drop-on-demand inkjet. The main
reasons for this are: (1) The high activity of the solvents towards the printhead materials; and (2) objectionable smell
and toxicity. In addition, for bubble-jet (but not for piezo inkjet), there are the additional problems in these solvent
systems of (1) poor bubble nucleation and (2) inadequate temperature control, both of which lead to overheating the
40 printheads. Moreover, when the solvent-based inks are not dried quickly by evaporation, they tend to penetrate deep
into the paper, thereby deteriorating the image quality.
[0007] An approach to improve the attributes described above are various 'emulsion' techniques. Emulsions repre-
sent a plurality of droplets of one liquid in another. Emulsions can be of two different types, e.g., oil-in-water (O/W) or
water-in-oil (W/O). In addition to this, emulsions can be microemulsions and macroemulsions. Microemulsions are
45 thermodynamically equilibrium systems. Some microemulsions are also known as "swollen micelles", which means
that they represent surfactant micelles with the oil solubilized inside. Typical microemulsion particle size is 5-50 nm.
Microemulsions are normally transparent or slightly bluish because of the very small particle size. On the other hand,
macroemulsions are not in thermodynamic equilibrium and do not form spontaneously, that is , they require mechanical
agitation for preparation. Furthermore, their particle size is larger, 50 nm and up. One of the common examples of
50 macroemulsions is milk. Finally, 'miniemulsions' are a special case of macroemulsions with smaller particle size, below
1 µm. They are not thermodynamically stable and do not form spontaneously; however, they can be made kinetically
stable, so that the particle size does not change with time.
[0008] The use of microemulsions in inkjet ink has been known in the art for several years. Thus, in the patent of
Wickramanayake et al., (U.S. Patent No. 5,226,957) entitled "Solubilization of Water-Insoluble Dyes via Microemulsions
55 for Bleedless, Non-Threading, High Print Quality Inks for Thermal Inkjet Printers", it is suggested to incorporate an oil-
soluble dye into a microemulsion, which contained solvents, surfactants, co-surfactants, and water. In another patent
of Wickramanayake (U.S. Patent No. 5,565,022, "Fast-Drying, Bleed-Free Inkjet Ink Compositions"), it is suggested
to incorporate a dye into a mixture of an organic solvent, surfactant, and water, so that the dye and water-insoluble

2
 EP 1 149 879 A2

solvent are solubilized by the surfactant. In U.S. Patent No. 5,643,357 (Brenton et al., "Liquid Crystalline Ink Compo-
sitions"), an ink composition is suggested, that contains a surfactant, and oil-or-alcohol-soluble dye, and water. The
formulation undergoes a phase transition upon heating from a microemulsion phase to a lamellar phase, which helps
to stratify the inks to the surface of the paper, when the printing substrate is heated. In the U.S. Patent No. 5,492,559
5 (Oliver et al., "Liquid Crystalline Microemulsion Ink Compositions"), an ink formulation is described containing an aque-
ous phase, oil phase, and surfactant, and an oil-soluble dye, such that the system undergoes a microemulsion-liquid
crystalline state transition with decreasing temperature. The idea is (with some variations) to solubilize water insoluble
"solvent" dyes in micelles, and thereby, produce water and smudgefast images.
[0009] All the known microemulsion formulations fall short of attaining a good print quality because of the excessive
10 ink penetration into the paper and wicking along the fibers. Also, the need remains in solvents that have less smell,
lower toxicity, and higher solubilizing capacity towards the solvent dyes. Finally, the need remains for a solvent system
that combines all these attributes together, which is not a trivial task.
[0010] A major formulation problem involved in this approach is the limited solubility of the solvent dyes in the mi-
croemulsion formulations. Indeed, in order to get the full benefits of water-based inks, that is, the good bubble nucleation
15 and temperature control, low toxicity and smell, and moderate viscosity, the weight percentage of the solvent in the
ink should not exceed 50%; more preferably, it should not exceed 20%. If one further assumes that the solvent dye is
completely water-insoluble and dissolves only in the solvent domains of the microemulsion, then, in order to get the
dye load of 3%, typical for drop-on-demand inkjet, one needs the solubility of the dye in the solvent to be at least 6%,
preferably at least 15%. Even higher solubility is in fact desired to prevent the spontaneous crystallization of the dyes
20 from the solution caused by temperature variations. 20-50% solubility of the dye is highly desirable. However, most
solvent dyes cannot be dissolved to such a degree in apolar oils conventionally used in microemulsion formulations.
The reason for this is the fact that most of the solvent dyes conventionally used in inkjet inks are not soluble in both
water and hydrocarbons.

25 SUMMARY OF THE INVENTION

[0011] The present invention relates to an aqueous inkjet ink composition comprising:

(a) dye molecules;

30 (b) micelles comprising a solvent of a formula R-S, S being a dye-solubilizing group and R being a hydrophobic
group; and
(c) an aqueous vehicle,

wherein the micelles are surrounded by the aqueous vehicle , each micelle having a monolayer surface enclosing an
35 inside area of the micelle, the hydrophobic groups (R) extending into the inside area of the micelle from the monolayer
surface and the dye-solubilizing groups (S) being at the monolayer surface of the micelles, and the dye molecules
associating with the dye-solubilizing groups (S) at the monolayer surface of the micelles, the micelles separating the
dye particles from the aqueous vehicle.
[0012] The present invention further relates to a method of making an aqueous inkjet ink composition comprising
40 the steps of:

a) forming micelles in an aqueous vehicle by adding chemical compounds to an aqueous vehicle, the chemical
compounds comprising a solvent of a formula R-S, R being a hydrophobic group and S being a dye-solubilizing
group, each micelle having a monolayer surface enclosing an inside area of the micelle, the hydrophobic groups
45 (R) extending into the inside area of the micelle and the dye-solubilizing groups (S) being at the monolayer surface
of the micelle; and
b) solubilizing dye molecules in the aqueous vehicle by adding dye molecules to the aqueous vehicle of a), the
dye molecules associating with the dye-solubilizers at the monolayer surface of the micelles, the micelles sepa-
rating the dye particles from the aqueous vehicle.
50
BRIEF DESCRIPTION OF THE DRAWINGS

[0013] Figure 1 shows the dye molecule (filled ellipse) on the left in non-structured solution of the dye solubilizing
group, S, (unfilled ellipse) in water (filled black circles). The solubility is reduced because of the unfavorable contact
55 between the dye and water. On the right when the dye solubilizing group, S, are structured with the help of grafted
hydrophobic tails, R, the solubility increases.
[0014] Figures 2 and 3 are color gamut charts showing the color performance of Microemulsion # 6 compared to the
color performance of Hewlett Packard HP2000C Ink Jet Printer on Hewlett Packard Professional Brochure & Flyer

3
 EP 1 149 879 A2

Paper, Two-Sided Gloss (Fig. 2) and Champion Data Copy office paper (Champion) (Fig. 3) respectively.
[0015] Figure 4 plots drops per 1/600 dpi against optical density for Microemulsion #6/Savinyl NS Black on Hewlett
Packard Professional Brochure & Flyer Paper, Two-Sided Gloss, Hewlett Packard Premium Inkjet Paper, and Champion
Data Copy office paper (Champion) papers.
5
DETAILED DESCRIPTION OF THE INVENTION

[0016] The present invention described herein is directed to inkjet inks for printing inkjet images using commercially
available inkjet printers such as, for example but not limited to, HP DeskJet® printers, manufactured by Hewlett-Packard
10 Company, of Palo Alto, California. The inks enable production of near photographic images having little or no coales-
cence, excellent waterfastness, and reduced dry time, on a range of print media, in particular, for example but not
limited to, plain white, 8 υ" X 11", 20 lb. weight, printer paper conventionally used for office and home computers.
[0017] As discussed above, there is a considerable demand for better permanence of inkjet images. Waterfastness,
highlighter smearfastness and stability to wet and dry finger smudge are especially desirable.
15 [0018] Attempts to achieve the above desirable qualities inkjet inks have lead to the formulation of water-based inks
with solvent-soluble dyes in microemulsions.
[0019] Microemulsions represent single-phase thermodynamically equilibrium mixtures of a surfactant, optionally, a
co-surfactant, an oil and water. Surfactant molecules consist of two blocks: a hydrocarbon tail, and a polar head. The
term "oil" is broadly used in this application and means any water-immiscible solvent, such as alkanes, esters or ethers.
20 Some other solvents that have more distinct surfactant-like structures, e.g., alcohols, are normally classified as "co-
surfactants". Finally "water" here means an aqueous solution of salts, or other water-compatible solvents such as
glycols or glycerol, or their water-soluble derivatives. The structure of a microemulsion represents water domains sep-
arated from the oil domains by a surfactant monolayer film. If a co-surfactant is present in the system, it tends to
assemble together with the co-surfactant, forming a mixed monolayer. Normally, the system represents small 1-10 nm
25 oil drops ("swollen micelles") dispersed in water, with the surfactant molecules assembled at the interface. However,
other surfactant assemblies, such as bilayer aggregates (lamellar phase, vesicles) are also possible. After the structure
is formed, the solvent soluble dye can be solubilized into the hydrophobic interior of the drops.
[0020] Solvent dyes are defined as dyes soluble in organic solvents and virtually insoluble in water. An extensive list
of solvent dyes can be found in Colour Index, Third edition, Volume 3, 1971, published by The society of Dyers and
30 Colourists, pp 3563 - 3648. For some of the solvent dyes, the solubility properties in a wide variety of organic solvents
have been determined. Thus, Clariant GmbH, Division of Pigments and Additives, BU Pigments, Frankfurt, Germany,
offers solvent dyes sold under the tradename Savinyl® Dyes. For all these dyes, the solubility in 19 solvents of various
polarity, such as water, hydrocarbons, alcohols, ketones, ethers and esters has been evaluated and this data is supplied
by the manufacturer. Closer inspection of the solubility tables reveals that the solvent dyes do not dissolve neither in
35 water nor in hydrocarbons (e. g., toluene or white spirit), but dissolve well in rather polar solvents, such as methanol,
ethanol, cyclohexanone, 2-pyrrolidone, methylethylketone or in oligoethylene or oligopropylene glycols. In addition to
the high polarity, specific chemical moieties in the structure of the solvent can drastically improve the solubility. These
chemical moieties are 5-6 membered rings (both saturated and aromatic), ether, and keto-groups. For example, all the
Savinyl solvent dyes have 250-500 g/l solubility in cyclohexanone, and most of them dissolve at > 100g/l in benzyl
40 alcohol. Similarly, as determined experimentally, 2-pyrrolidinone, tetraethylene glycol, and polyethylene glycol (M=400)
dissolve Savinyl Yellow RLS, Savinyl Pink 6BLS, Savinyl Blue GLS, and Savinyl Black NS at ,> 33 wt%. For simplicity,
these solvents will be called below "dye solubilizers" and abbreviated as S. The mechanism of their solvent action is
unclear, but apparently represents a combination of polarity match plus specific interactions with the dye chromophores.
However, traditional microemulsions cannot be formulated with these solvents, because they are water-miscible. More-
45 over, the non-structured, binary mixtures of these solvents with water are not effective in solubilizing the solvent dyes.
Experiments show that the solubility in such mixed solvents is lower than required, even when the solvent load is very
high, > 50%, (see the Tables in Example 1).
[0021] The present inventor has found that in order to effectively solubilize the solvent dyes in aqueous solution with
dye-solubilizing solvents in a microemulsion system, it is important to induce the microscopic separation of dye solu-
50 bilizing groups of the solvent from the water. One way to achieve this (as shown in Figure 1) is to graft hydrophobic
groups, R, to the dye-solubilizing moieties, S. In an aqueous solution, the hydrophobic groups self-associate and form
a micelle, with the dye-solubilizing groups at the surface of the micelle, this micelle surface known as the "palisade
layer"1. The dyes can then be solubilized into the micellar palisade layer. As opposed to the plain binary mixture of
the S and water, the dyes have a much higher solubility in this system, because direct contact of the dye with water is
55 avoided.
[0022] One embodiment of this solvent having both dye-solubilizing solvents and grafted hydrophobic groups is alkyl-
1 B. Jönsson, H. Wennerström, Phase Equilibria in a Three-Component Water-Soap-Alcohol System: A Thermodynamic Model, J. Phys. Chem., 91
(1987) 338.

4
 EP 1 149 879 A2

substituted 2-pyrrolidinones (also known as alkyl-substituted 2-pyrrolidones). These solvents have very little smell, no
toxicity and dissolve many solvent dyes. Non-substituted 2-pyrrolidinone itself is polar and completely miscible with
water. Alkyl-substituted 2-pyrrolidinones must be therefore regarded as weak surfactants themselves, akin to microe-
mulsion "co-surfactants", which are normally medium-chain alcohols. In conjunction with this solvent, a variety of an-
5 ionic surfactants can be used. Nonlimiting examples of such anionic surfactants are alkylsulfates, alkylcarboxylates
and alkylsulfonates, as well as nonionic surfactants.
[0023] In another embodiment, the dye-solubilizing group is an oligo(ethylene glycol) -(CH2CH2O)nH, where n = 1-
50. Here various hydrophobic tails R connected to the dye-solubilizing group by an ether or ester bond can be used,
For example, one can use ethoxylated alcohols CmH2m+1(CH2CH2O)nH with m = 4 - 20 and n = 1- 50. One of the
10 possible candidates is an ethoxylated alcohol with m = 8 and n = 5, or with m=4 and n = 2. Similarly one can use
commercial ethoxylated surfactants, such as Tween 20, or Tween 80.
[0024] In one embodiment, the present invention relates to an aqueous inkjet ink composition comprising:

(a) dye molecules;

15 (b) micelles comprising a solvent of a formula R-S, S being a dye-solubilizing group and R being a hydrophobic
group; and
(c) an aqueous vehicle,

wherein the micelles are surrounded by the aqueous vehicle , each micelle having a monolayer surface enclosing an
20 inside area of the micelle, the hydrophobic groups (R) extending into the inside area of the micelle from the monolayer
surface and the dye-solubilizing groups (S) being at the monolayer surface of the micelles, and the dye molecules
associating with the dye-solubilizing groups (S) at the monolayer surface of the micelles, the micelles separating the
dye particles from the aqueous vehicle.
[0025] In another embodiment, the present invention relates to a method of making an aqueous inkjet ink composition
25 comprising the steps of:

a) forming micelles in an aqueous vehicle by adding chemical compounds to an aqueous vehicle, the chemical
compounds comprising a solvent of a formula R-S, R being a hydrophobic group and S being a dye-solubilizing
group, each micelle having a monolayer surface enclosing an inside area of the micelle, the hydrophobic groups
30 (R) extending into the inside area of the micelle and the dye-solubilizing groups (S) being at the monolayer surface
of the micelle; and
b) solubilizing dye molecules in the aqueous vehicle by adding dye molecules to the aqueous vehicle of a), the
dye molecules associating with the dye-solubilizing groups at the monolayer surface of the micelles, the micelles
separating the dye particles from the aqueous vehicle.
35
[0026] In preferred embodiments of the above-described composition and method, the micelle further comprises
surfactants. In more preferred embodiments, the micelle further comprises co-surfactants.
In other preferred embodiments of the above-described composition and method, the dye-solubilizing groups are de-
rived from polar molecules selected from the group consisting of methanol; ethanol; cyclohexanone; 2-pyrrolidone;
40 methylethylketone; oligoethylene glycols, (CH2CH2O)nH (n = 1 - 50) and oligopropylene glycols, (CH(CH3)CH2O)mH
(m = 1 - 50). In more preferred embodiments, the dye-solubilizing groups are derived from oligoethylene glycols selected
from the group consisting of diethylene glycol, tetraethylene glycol and octaethylene glycol. In other more preferred
embodiments, the dye-solubilizing groups are derived from oligopropylene glycols selected from the group consisting
of dipropylene glycol, tetrapropylene glycol and octapropylene glycol. In yet other more preferred embodiments, the
45 hydrophobic groups have from 4 to 20 carbon atoms.
[0027] In yet other preferred embodiments of the above-described composition and method, the hydrophobic group
(R) and the solubilizing group (S) form the solvent of the formula R-S with a bond between R and S selected from a
carbon-carbon bond, a carbon-oxygen ether bond, a carbon-oxygen ester bond, a carbon-nitrogen amine bond and a
carbon-nitrogen amide bond.
50 [0028] In still other preferred embodiments of the above-described composition and method, the aqueous inkjet ink
composition is comprised of from 1 to 5 wt. percent dye.
[0029] In yet other preferred embodiments of the above-described composition and method, the aqueous inkjet ink
composition is comprised of from 5 to 50 wt. percent of the solvent having the formula R-S.
[0030] In still other preferred embodiments of the above-described composition and method, the aqueous inkjet ink
55 composition is comprised of from 50 to 80 wt. percent of the aqueous vehicle.
[0031] In yet other preferred embodiments of the above-describedcomposition and method, the dye molecules are
selected from the group consisting of Cl Solvent Yellow 79, Cl Solvent Yellow 83:1, Cl Solvent Yellow 83, Cl Solvent
Yellow 62, Cl Solvent Orange 41, Cl Solvent Orange 62, Cl Solvent Red 92, Cl Solvent Red 124, Cl Solvent Red 8, Cl

5
 EP 1 149 879 A2

Solvent Red 91, Cl Solvent Red 127, Cl Acid Violet 66, Cl Solvent Blue 45, Cl Solvent Blue 44, Cl Solvent Black 45,
Cl Solvent Black 27, Solvent Red 217, Solvent Red 218, Neozapon Red 395, Solvent Blue 35, Solvent Black 27, Savinyl
Yellow RLS, Savinyl Pink 6BLS, Savinyl Blue GLS, and Savinyl Black NS.

5 EXAMPLES

Example 1. Typical Microemulsion Formulations.

[0032] Some typical microemulsion formulations studied are shown in Tables 1 through 11 below. As S in R-S-sol-
10 vents, 2-pyrrolidonyl and oligo(ethylene oxide) groups were used. The systems additionally contained humectants and,
in some cases, surfactants. All the systems studied were water-based and were in single-phase state at room temper-
ature.

Table 1
15
Microemulsion #1
Component wt%
1-Octyl-2-pyrrolidone (Aldrich) 7
Dodecane (Aldrich) 3
20
Sodium dodecyl sulfate (Sigma) 1
Diethylene glycol (Aldrich) 3.6
2-Pyrrolidone (Aldrich) 3.6
Glycerol (Aldrich) 9
25 Trizma Base (Aldrich) 0.18
Proxel GXL (ICI) 0.18
EDTA disodium salt (Aldrich) 0.18
water balance

30
Table 2
Microemulsion #2
Component wt%
35
1-Octyl-2-pyrrolidone (Aldrich) 20
Dodecane (Aldrich) 2.6
Sodium dodecyl sulfate (Sigma) 2
Diethylene glycol (Aldrich) 3
40 2-Pyrrolidone (Aldrich) 3
Glycerol (Aldrich) 7.5
Trizma Base (Aldrich) 0.15
Proxel GXL (ICI) 0.15
EDTA disodium salt (Aldrich) 0.15
45
water balance

Table 3

50 Microemulsion #4
component wt%
1-Octyl-2-pyrrolidone (Aldrich) 10
sodium octylsulfonate (Sigma) 1
55 Diethylene glycol (Aldrich) 3.6
2-Pyrrolidone (Aldrich) 3.6
Glycerol (Aldrich) 9

6
 EP 1 149 879 A2

Table 3 (continued)
Microemulsion #4
component wt%
5 Trizma Base (Aldrich) 0.18
Proxel GXL (ICI) 0.18
EDTA disodium salt (Aldrich) 0.18
water balance
10

Table 4
Microemulsion #5
component wt%
15
1-Octyl-2-pyrrolidinone (Aldrich) 16.7
lithium octanoate (Aldrich*) 1.72
Diethylene glycol (Aldrich) 3.3
2-Pyrrolidone (Aldrich) 3.3
20
Glycerol (Aldrich) 8.3
Trizma base (Aldrich) 0.17
Proxel GXL (ICI) 0.17
EDTA disodium salt (Aldrich) 0.17
25 water balance
*prepared by neutralization of n-octanoic acid by lithium hydroxide

Table 5
30
Microemulsion #6
component wt%
1-Hexyl-2-pyrrolidone (BASF) 16.7
lithium octanoate* (Aldrich) 1.72
35
Diethylene glycol (Aldrich) 3.3
2-Pyrrolidone (Aldrich) 3.3
Glycerol (Aldrich) 8.3
Trizma base (Aldrich) 0.17
40 Proxel GXL (ICI) 0.17
EDTA disodium salt (Aldrich) 0.17
water balance
*prepared by neutralization of n-octanoic acid by lithium hydroxide

45

Table 6
Microemulsion #7
component wt%
50
1-Hexyl-2-pyrrolidinone (BASF) 16.7
Tetramethyl ammonium 2.3
octanoate* (Aldrich)
Diethylene glycol (Aldrich) 3.3
55
2-pyrrolidone (Aldrich) 3.3
Glycerol (Aldrich) 8.3
*prepared by neutralization of n-octanoic acid by tetramethylammonium hydroxide

7
 EP 1 149 879 A2

Table 6 (continued)
Microemulsion #7
component wt%
5 Trizma base (Aldrich) 0.17
Proxel GXL (ICI) 0.17
EDTA disodium salt (Aldrich) 0.17
water balance
10

Table 7
Microemulsion #13
component wt%
15
Tergitol NP-10 (Union Carbide) 10
Diethylene glycol (Aldrich) 3.3
2-Pyrrolidone (Aldrich) 3.3
Glycerol (Aldrich) 8.3
20
Trizma base (Aldrich) 0.17
Proxel GXL (ICI) 0.17
EDTA disodium salt (Aldrich) 0.17
water balance
25

Table 8
Microemulsion #18
component wt%
30
n-octoxy(pentaethylene oxide)ol 20
Diethylene glycol (Aldrich) 3.3
2-Pyrrolidone (Aldrich) 3.3
Glycerol (Aldrich) 8.3
35
Trizma base (Aldrich) 0.17
Proxel GXL (ICI) 0.17
EDTA disodium salt (Aldrich) 0.17
water balance
40

Table 9
Microemulsion #32
component wt%
45
Tween-20 (ICI) 20
Diethylene glycol (Aldrich) 3.3
2-Pyrrolidone (Aldrich) 3.3
Glycerol (Aldrich) 8.3
50
Trizma base (Aldrich) 0.17
Proxel GXL (ICI) 0.17
EDTA disodium salt (Aldrich) 0.17
water balance
55

8
 EP 1 149 879 A2

Table 10
Microemulsion #33

5 component wt%
Tween-80 (ICI) 20
Diethylene glycol (Aldrich) 3.3
2-Pyrrolidone (Aldrich) 3.3
Glycerol (Aldrich) 8.3
10
Trizma base (Aldrich) 0.17
Proxel GXL (ICI) 0.17
EDTA disodium salt (Aldrich) 0.17
water balance
15

Table 11
Microemulsion #34

20 component wt%
Lithium octanoate* (Aldrich) 2
Diethylene glycol monohexyl ether 49
(Union Carbide)
water 49
25
*prepared by neutralization of n-octanoic acid by lithium hydroxide

Example 2. Viscosities of some of the microemulsions studied

30 [0033] Viscosities, shown in Table 12, were measured using a VE System (Vilastic Scientific, Inc.) at 25 °C. Ten
measurements were made over the range of shear rates from 10 to 200 s-1. The flow was Newtonian in all cases.

Table 12
System Viscosity, cP
35
Microemulsion #4 5.4
Microemulsion #5 7.3
Microemulsion #6 3.7

40 Microemulsion #7 3.7
Microemulsion #13 4.3
Microemulsion #18 5.1

45 Example 3. Physical Stability of Microemulsions

[0034] Microemulsions #1 and #6 were subjected to thermal variations between 5 °C and 60°C, and to freeze-thaw
cycle between -30 °C and room temperature. No phase separation occurred. After freeze-thaw cycle, the systems
remained single-phase and became slightly opalescent; the turbidity disappeared on standing..
50
Example 4. Solubility of Savinyl Dyes in microemulsions studied.

[0035] Solubility of dyes in microemulsions was accessed the following way. Dry dye was added to a microemulsion
at around 3 wt%. The sample was placed on rollers and mixed overnight. A 100 µl sample of supernatant was collected
55 and filtered through 0.22 µm filter, after which it was diluted by ethanol by a factor of 1:1000 - 1: 10000 w/w. The
concentration of the dye was determined spectrophotometrically by using a calibration constructed with solutions of
the dye in ethanol. The results are shown in Tables 13. In some cases, the solubility was accessed visually as judged
by complete dissolution of the solid dye; these data are shown in Table 14.

9
 EP 1 149 879 A2

Table 13
Solubility of Savinyl Solvent Dyes from Clariant in various microemulsion systems, wt% (spectrophotometric data)

5 Dye M #1 M #5 M #6 M #7 M #2 M #11 M #13 M #18 M #32 M #33

Savinyl blue GLS 1.2 >2.66 >2.36 >2.45 >2.85 0.83 1.02 1.90 0.84 0.89
(668
nm)
Savinyl Pink 6BLS 1.7 >3.47 >3.43 >3.33 >3.30 1.88 2.52 >3.14 0.90 1.08
10
(542 nm)
Savinyl yellow 2.0 >2.97 >2.64 >2.71 >2.91 0.45 0.79 1.48 1.46 1.60
RLS(430 nm)
Savinyl black NS No data >2.97 >3.09 >2.89 >2.95 0.47 0.49 0.92 >4.17 2.44
15 (580 nm)

Table 14
Solubility of Savinyl Solvent Dyes from Clariant in Microemulsion #6, wt% (visual inspection)
20
Dye M #6
Savinyl fire red 3GLS >3
Savinyl black RLSN >3
Savinyl blue RLS <3
25
Savinyl yellow RLSN >3
Savinyl Yellow 2GLS >3
Savinyl yellow 2RLS >3
Savinyl red 3BLS >3
30
Example 5 (comparative). Solubility of Savinyl dyes in microemulsions versus solubility in non-structured
solvents and solvent mixtures

[0036] Solubilities of four Savinyl dyes (Clariant) were measured in water, 2-pyrrolidone, water-2-pyrrolidone binary
35 mixtures, as well as in two octyl-2-pyrrolidone-based Microemulsions #1 and #2 . The results are outlined in Table 15.

Table 15.
Solubility of Savinyl Dyes in water,2-pyrrolidone, water-2-pyrrolidone binary mixtures, and octyl-2-pyrrolidone-based
microemulsions
40
Solvent Savinyl Yellow RLS Savinyl Pink BLS Savinyl Blue GLS Savinyl Black NS
Water <0.1% <0.1% <0.1% <0.1%
2-Pyrrolidone (2-P) >33% >33% >33% >33%

45 20% 2P-80% water 0.3% 0.2% 0.1% 0.3%

50% 2P-50% water 0.3% 0.2% 0.1% 0.3%
Microemulsion #1 (containing 2.0% 1.7% 1.2% no data
7% octyl-2-pyrrolidone)
50 Microemulsion #2 (containing >2.91% >3.3% >2.85% >2.95%
20% octyl-2-pyrrolidone)

[0037] From Table 15, one can see that 2-Pyrrolidone (2-P) is an excellent solvent for Savinyl solvent dyes, and
water is a very poor solvent. Binary mixtures of 2-P and water, even when the solvent load of 2-P in the system is as
55
high as 50 wt%, dissolve the dyes at merely few tenths of percent. On the other hand, microemulsion systems, con-
taining 7 and 20 wt% of octyl-2P, respectively, dissolve the dyes on the level of several percents.

10
 EP 1 149 879 A2

Example 6 (comparative). Solubility of Savinyl dyes in microemulsions versus solubility in non-structured

solvents and solvent mixtures

[0038] Solubilities of Savinyl dyes in water, tetraethylene glycol, water-tetraethylene glycol binary mixtures, aqueous
5 solutions of ethoxylated surfactants (microemulsions 13 and 18) are given in Table 16.

Table 16.
Solubility of Savinyl Dyes in water, tetraethylene glycol, water-tetraethylene glycol binary mixtures, and aqueous
solutions of ethoxylated surfactants
10
Solvent Savinyl Yellow RLS Savinyl Pink BLS Savinyl Blue GLS Savinyl Black NS
Water <0.1% <0.1% <0.1% <0.1%
Tetra(ethylene glycol), {TEG}, >33% >33% >33% >33%
15
(Aldrich)
20% TEG-80% water 0.07% 0.03% 0.05% 0.16%
50% TEG-50% water 0.23% 0.31% 0.15% 0.48%
Microemulsion #13 0.79% 2.52% 1.02% 0.49%
20 (containing 10% of Tergitol
NP-10, Union Carbide)
Microemulsion #18 1.48% 3.14% 1.90% 0.92%
(containing 20% n-octyl-
OCH2CH2)5OH
25

[0039] From Table 16, one can see that again, tetraethylene glycol (TEG) is an excellent solvent for Savinyl solvent dyes,
and water is a poor solvent. Their binary mixtures are not effective solvents, and even 50-50 mixture of water and TEG
dissolves less than 1% of the dyes. On the other hand, solutions of surfactants, such as Tergitol NP-10 and n-octyl
(OCH2CH2)5OH have a significantly higher solubilization capacity at much lower concentration in the formulation. Structurally,
30
Tergitol NP-10 surfactant represents a nonylphenol ether of ethylene oxide, containing on average 10 ethylene oxide groups.

Example 7. Printability and color gamut of microemulsion inks

[0040] Savinyl dyes from Clariant: Savinyl Blue GLS, Savinyl Yellow RLS, and Savinyl Pink 6BLS were dissolved in
35
Microemulsions #1 and #6. In order to dissolve the dye, 3% of a dry dye was added to the microemulsion and the system
was left on rolls overnight. For Microemulsion #6, the dissolution was complete; for Microemulsion #1, the dissolution was
not complete and the inks were filtered from the excess dye. The inks were then filled into color printheads of an HP 2000c
Hewlett Packard printer. Th inks showed good print quality on office and special inkjet papers, specifically, no missing
nozzles, controlled wicking and almost instant drying. The color gamut volume was somewhat less than that of the
40
HP2000c, as shown in Figures 2 and 3. The ink flux per unit area was 8 pL per 1/600 sq. inch for primary and 16 pL per
1/600pL secondary colors for HP2000c default inks and for Microemulsion #6; it was x2 higher for Microemulsion #1 inks.

Example 8. Performance of a microemulsion-based black

45
[0041] 3% of Savinyl Black NS was added as a dry powder to Microemulsion # 6. The sample was put on rolls
overnight and a color pen of an HP2000c Hewlett Packard printer was filled. The inks printed well both on the office
and special offset papers. Wicking was moderate and optical density was good, as shown in Figure 4, which represents
the plot of the black optical density versus the number of drops per 1/600-inch pixel.
50
Example 9. Durability of microemulsion inks (waterfastness, wet smudge, highlighter smear).

[0042] Savinyl dyes from Clariant: Savinyl Blue GLS, Savinyl Yellow RLS, and Savinyl Pink 6BLS were dissolved in
Microemulsions #6 and #7 at 3 wt%. Waterfastness to passive water drip was evaluated by dripping 200 ml of water
on a printout tilted at 45 degrees. The optical density transfer between the rectangular bars was measured using a
55
MacBeth spectrophotometer. Wet smudge was measured similarly, with the difference that after dripping the water,
the image was smudged by finger in a rubber glove. Alkaline highlighter smear was measured by using a Major Accent
Highlighter (Sanford). The results of testing are summarized in Tables 17 and 18.

11
 55

50

45

40

35

30

25

20

15

10

5
Table 17.
Durability of microemulsion inks (10 minutes after printing)
Paper dyes waterfast ness wet smudge Initial Optical Highlighter smear, Highlighter smear, Highlighter smear, Microe mulsion
Density 1pass 2pass 3pass system
HP Premium Cyan 0.06 0.06 0.97 0.00 0.02 0.06 M#6
Inkjet paper
same Magenta 0.10 0.10 1.31 0.01 0.12 0.16 M#6
same Yellow 0.03 0.03 1.03 n/a n/a n/a M#6
same
HP Cyan 0.00 0.01 0.98 0.00 0.00 0.01 M#6
Professional
Brochure
paper
same Magenta 0.16 0.02 1.44 0.02 0.03 0.04 M#6

EP 1 149 879 A2
same Yellow 0.00 0.00 1.12 n/a n/a n/a M#6
same Black 0.01 0.04 1.60 0.01 0.04 0.06 M#7
Champion Cyan 0.14 0.06 0.81 0.00 0.01 0.02 M#6
12

Data Copy
Paper
same Magenta 0.12 0.19 0.96 0.00 0.02 0.02 M#6
same Yellow 0.07 0.07 0.80 n/a n/a n/a M#6
same Black 0.04 0.09 0.99 0.00 0.01 0.01 M#7
 EP 1 149 879 A2

[0043] It has been found that moderate heat after printing improves the durability considerably. Table 18 shows the
durability results after heat treatment of the prints with a heat gun (, 100 C for 1 minute).

10

15

20

25

30

35

40

45

50

55

13
 55

50

45

40

35

30

25

20

15

10

5
Table 18.
Durability of heated samples
Paper dyes waterfast ness wet smudge Initial Optical Highlighter smear, Highlighter smear, Highlighter smear, Microemulsion
Density 1pass 2pass 3pass system
HP Cyan 0.01 0.01 0.95 0.00 0.00 0.00 M#6
Professional
Brochure
paper
same Magenta 0.05 0.15 1.41 0.00 0.01 0.06 M#6
same Yellow 0.00 0.01 1.07 n/a n/a n/a M#6
same Black 0.00 0.04 1.52 0.00 0.01 0.09 M#7
Champion Cyan 0.02 0.03 0.75 0.00 0.00 0.01 M#6
Data Copy
Paper

EP 1 149 879 A2
same Magenta 0.11 0.11 0.98 0.07 0.10 0.12 M#6
same Yellow 0.07 0.01 0.81 n/a n/a n/a M#6
same Black 0.00 0.03 1.02 0.00 0.00 0.00 M#7
14
 EP 1 149 879 A2

[0044] From Tables 17 and 18, one can see that a substantial level of durability can be attained for cyan, yellow and
black; worse results are seen for magenta.

Example 10. Lightfastness of microemulsion inks

5
[0045] Lightfastness of the inks prepared based on Microemulsions #1 (Savinyl Blue GLS, Savinyl Yellow RLS, and
Savinyl Pink 6BLS dissolved to saturation) and Microemulsion #6 (Savinyl Black NS dye dissolved at 3%). The testing
was done using an Atlas HPUV indoor exposure system, with 1 yr. exposure simulated. The loss of optical density
(OD) after exposure is shown in Table 19 below.
10
Table 19.
Optical density loss of microemulsion inks after 1 year exposure outdoors (simulated), 1 yr. = 1971 kLux x hr.
Hammermill Fore DP HP Premium Inkjet Paper HP Premium Brochure Paper
15 OD OD 1 yr. ratio OD before OD 1 yr. ratio OD before OD 1 yr. ratio
before
cyan M#1 0.48 0.47 0.98 0.58 0.54 0.93 0.61 0.58 0.95
0.81 0.79 0.98 0.98 1 1.02 1.06 1.09 1.03
20 magenta 0.51 0.31 0.61 0.5 0.21 0.42 0.61 0.28 0.46
M#1
0.91 0.7 0.77 0.92 0.41 0.45 1.12 0.65 0.58
yellow 0.59 0.56 0.95 0.63 0.58 0.92 0.75 0.71 0.95
M#1
25 0.9 0.85 0.94 1.13 1.11 0.98 1.19 1.15 0.97
black M#6 0.49 0.484 0.99 0.47 0.47 1.00 0.5 0.5 1.00
0.99 0.99 1.00 1.17 1.17 1.00 0.95 0.94 0.99

[0046] From Table 19, one can see that cyan, yellow and black show only minimal loss in optical density and are
30
lightfast. On the other hand, magenta is not lightfast enough.

Example 11. Gloss levels of microemulsion inks

[0047] In the Table 20 below, the gloss levels of Microemulsion #1 based inks, described in Example 7, are shown
35
on HP Professional Brochure and Flyer Paper, at the same ink flux as in Example 7. For comparison, Hewlett Packard
LaserJet 4500 gloss levels are shown. The measurements were done at 60 degrees using a Micro-TRI-glossmeter
(Gardener).

Table 20.
40
Gloss levels of Microemulsion #1-based inks versus those of LaserJet 4500
Printer No colorant (control) Cyan Magenta Yellow Red Green Blue
Ink of this invention 51.2 47.4 47.5 47.4 37.8 36.8 35.6
45 LaserJet 4500 45.7 3.1 3.2 3.9 3.7 3.3 3.1

[0048] Obviously, the inks of the current invention conserve the gloss of the paper to a considerable degree, while
LaserJet substantially reduces the gloss.

50 Example 12 Durability and lightfastness of other solvent-dye-based microemulsion inks

[0049] The Savinyl dyes from Clariant: Black RLSN, Blue RLS, Red 3 BLS, Fire Red 3 GLS, Yellow 2 GLS, Yellow
2 RLS, and Yellow RLSN have been dissolved in Microemulsion #6 at 3% . The dissolution was complete for all the
dyes except for the blue. The solutions were filtered through 0.45 µm filter and were filled into color pens of HP 2000c
55 Hewlett Packard printer. The inks printed well and did not show significant wicking on office paper. The inks showed
excellent lightfastness, as measured by the method described in Example 10, (Table 21), and durability , as measured
by the methods described in Example 9 (Table 22).

15
 EP 1 149 879 A2

Table 21.
Lightfastness of Savinyl Dyes in Microemulsion #6 (1 yr. simulated)

5 Paper: Hammermill Fore DP optical density

before fade after fade fading ratio
1. Savinyl Black RLSN 1.08 0.608 1.06 0.61 0.98 1.00
2. Savinyl Blue RLS 0.372 0.108 0.337 0.1 0.91 0.93
10 3. Savinyl Red 3 BLS 0.922 0.268 0.911 0.272 0.99 1.01
4. Savinyl Fire Red 3 GLS 1.04 0.372 0.972 0.331 0.93 0.89
5. Savinyl Yellow 2 GLS 0.858 0.282 0.802 0.178 0.93 0.63
6. Savinyl Yellow 2 RLS 0.839 0.238 0.859 0.267 1.02 1.12
7. Savinyl Yellow RLSN 0.97 0.323 0.951 0.335 0.98 1.04
15

HP brochure paper

1. Savinyl Black RLSN 1.52 0.975 1.52 0.947 1.00 0.97

20
2. Savinyl Blue RLS 0.389 0.099 0.336 0.099 0.86 1.00
3. Savinyl Red 3 BLS 1.2 0.282 1.18 0.293 0.98 1.04
4. Savinyl Fire Red 3 GLS 1.52 0.362 1.5 0.288 0.99 0.80
5. Savinyl Yellow 2 GLS 1.15 0.222 1.13 0.249 0.98 1.12
25 6. Savinyl Yellow 2 RLS 1.04 0.227 1.03 0.259 0.99 1.14
7. Savinyl Yellow RLSN 1.23 0.316 1.22 0.334 0.99 1.06

Table 22.
30
Durability of Savinyl Dyes in Microemulsion # 6
PAPER: Hammermill Fore DP
wet smudge waterfastness highlighter smear

35
Black RLSN: 0.04 0.01 0.01 1 pass Alkali
0.02 2pass Alkali
0.02 3pass Alkali
0.01 1 pass Acid
0.02 2pass Acid
40 0.04 3pass Acid
Blue RLS 0.00 0.00 0.00 1pass Alkali
0.00 2pass Alkali
0.00 3pass Alkali
0.00 1pass Acid
45
0.00 2pass Acid
0.00 3pass Acid
Red 3BLS no data no data 0.00 1 pass Alkali
0.00 2pass Alkali
50 0.01 3pass Alkali
0.00 1pass Acid
0.00 2pass Acid
0.01 3pass Acid
Fire Red 3GLS 0.04 0.03 0.02 1pass Alkali
55
0.01 2pass Alkali
0.01 3pass Alkali
0.05 1pass Acid

16
 EP 1 149 879 A2

Table 22. (continued)

Durability of Savinyl Dyes in Microemulsion # 6
PAPER: Hammermill Fore DP
5
wet smudge waterfastness highlighter smear
0.04 2pass Acid
0.05 3pass Acid
Yellow 2 RLS 0.09 0.07 n/a n/a
10 Yellow 2 RLSN 0.02 0.04 n/a n/a
Yellow 2 GLS 0.02 0.01 n/a n/a
HP Brochure paper

15 Black RLSN: 0.00 0.00 0.00 1pass Alkali

0.00 2pass Alkali
0.00 3pass Alkali
0.00 1pass Acid
0.00 2pass Acid
20
0.00 3pass Acid
Blue RLS 0.00 0.00 0.00 1pass Alkali
0.00 2pass Alkali
0.01 3pass Alkali
25 0.00 1pass Acid
0.00 2pass Acid
0.00 3pass Acid
Red 3BLS 0.00 0.00 0.00 1pass Alkali
0.01 2pass Alkali
30
0.04 3pass Alkali
Fire Red 3GLS No data No data 0.01 1pass Acid
0.03 2pass Acid
0.04 3pass Acid
35 Yellow 2 RLS 0.00 0.00 n/a n/a
Yellow 2 RLSN 0.00 0.00 n/a n/a
Yellow 2 GLS 0.01 0.00 n/a n/a

40 Claims

1. An aqueous inkjet ink composition comprising:

(a) dye molecules;

45 (b) micelles comprising a solvent of a formula R-S, S being a dye-solubilizing group and R being a hydrophobic
group; and
(c) an aqueous vehicle,

wherein the micelles are surrounded by the aqueous vehicle , each micelle having a monolayer surface enclosing
50 an inside area of the micelle, the hydrophobic groups (R) extending into the inside area of the micelle from the
monolayer surface and the dye-solubilizing groups (S) being at the monolayer surface of the micelles, and the dye
molecules associating with the dye-solubilizing groups (S) at the monolayer surface of the micelles, the micelles
separating the dye particles from the aqueous vehicle.

55 2. An aqueous inkjet ink composition of claim 1, wherein the micelles further comprise surfactants.

3. An aqueous ink of claim 2, wherein the micelles further comprise co-surfactants.

17
 EP 1 149 879 A2

4. The aqueous inkjet ink composition of claim 1, wherein the dye-solubilizing groups are derived from polar molecules
selected from the group consisting of methanol; ethanol; cyclohexanone; 2-pyrrolidone; methylethylketone; oli-
goethylene glycols, (CH2CH2O)nH, where n is from 1 to 50; and oligopropylene glycols, (CH (CH3)CH2O)mH, where
m is from 1 to 50.
5
5. The aqueous inkjet ink composition of claim 4, wherein the dye-solubilizing groups are derived from oligoethylene
glycols selected from the group consisting of diethylene glycol, tetraethylene glycol and octaethylene glycol.

6. The aqueous inkjet ink composition of claim 4, wherein the dye-solubilizing groups are derived from oligopropylene
10 glycols selected from the group consisting of dipropylene glycol, tetrapropylene glycol and octapropylene glycol.

7. The aqueous inkjet ink composition of claim 4, wherein the hydrophobic group has from 4 to 20 carbon atoms.

8. The aqueous inkjet ink composition of Claim 1, wherein the hydrophobic group (R) and the solubilizing group (S)
15 form the solvent of the formula R-S with a bond between R and S selected from a carbon-carbon bond, a carbon-
oxygen ether bond, a carbon-oxygen ester bond, a carbon-nitrogen amine bond and a carbon-nitrogen amide bond.

9. The aqueous inkjet ink composition of claim 1, wherein the aqueous inkjet ink composition is comprised of from 1
to 5 wt. percent dye.
20
10. The aqueous inkjet ink composition of claim 1, wherein the aqueous inkjet ink composition is comprised of from 5
to 50 wt. percent of the solvent having the formula R-S.

11. The aqueous inkjet ink composition of claim 1, wherein the aqueous inkjet ink composition is comprised of from
25 50 to 80 wt. percent of the aqueous vehicle.

12. The aqueous inkjet ink composition of claim 1, wherein the dye molecules are selected from the group consisting
of Cl Solvent Yellow 79, Cl Solvent Yellow 83:1, Cl Solvent Yellow 83, Cl Solvent Yellow 62, Cl Solvent Orange 41,
Cl Solvent Orange 62, Cl Solvent Red 92, Cl Solvent Red 124, Cl Solvent Red 8, Cl Solvent Red 91, Cl Solvent
30 Red 127, Cl Acid Violet 66, Cl Solvent Blue 45, Cl Solvent Blue 44, Cl Solvent Black 45, Cl Solvent Black 27,
Solvent Red 217, Solvent Red 218, Neozapon Red 395, Solvent Blue 35, Savinyl Yellow RLS, Savinyl Pink 6BLS,
Savinyl Blue GLS, and Savinyl Black NS.

13. A method of making an aqueous inkjet ink composition as claimed in any of claims 1 to 12 comprising the steps of:
35
a) forming micelles in an aqueous vehicle by adding chemical compounds to an aqueous vehicle, the chemical
compounds comprising a solvent of a formula R-S, R being a hydrophobic group and S being a dye-solubilizing
group, each micelle having a monolayer surface enclosing an inside area of the micelle, the hydrophobic
groups (R) extending into the inside area of the micelle and the dye-solubilizing groups (S) being at the mon-
40 olayer surface of the micelle; and
b) solubilizing dye molecules in the aqueous vehicle by adding dye molecules to the aqueous vehicle of a),
the dye molecules associating with the dye-solubilizers at the monolayer surface of the micelles, the micelles
separating the dye particles from the aqueous vehicle.

45

50

55

18
EP 1 149 879 A2

19
EP 1 149 879 A2

20
EP 1 149 879 A2

21
EP 1 149 879 A2

22