Compositions: coating or plastic – Coating or plastic compositions – Marking
Reexamination Certificate
2002-01-07
2003-08-12
Klemanski, Helene (Department: 1755)
Compositions: coating or plastic
Coating or plastic compositions
Marking
C106S031770, C106S496000, C008S641000
Reexamination Certificate
active
06605144
ABSTRACT:
This application is the National Phase of International Application PCT/GB00/01123 filed Mar. 24, 2000 which designated the United States and that International Application was published under PCT Article 21(2) in English. International Application PCT/GB00/01123 claims priority from Provisional Application 60/144061, filed Jun. 7, 1999, and also claims priority from GB 9907270.4, filed Mar. 30, 1999.
This invention relates to high light-fastness yellow compositions and to their use in ink jet printing (“IJP”). IJP is a non-impact printing technique in which droplets of coloured liquids are ejected through a fine nozzle onto a substrate without bringing the nozzle into contact with the substrate.
IJP is a relatively inexpensive way of recording multicolour images, for example pictures obtained from digital sources such as electronic cameras, scanners and the Internet. The use of ink jet printers to print colour images in the home or office environment is now becoming commonplace. However IJP has a big disadvantage compared to conventional silver halide photography in that the resultant images fade quite quickly in ordinary daylight. There is a need to improve the light-fastness properties of prints to prevent images vanishing or becoming discoloured over time.
We have now found that a composition comprising two particular yellow dyes defined below in a particular range of ratios has superior light-fastness compared to the individual dyes when printed on commercially available glossy film from Seiko Epson Corporation. The light-fastness is still not as good as for silver halide photographs but the composition does represent a step in the right direction towards improved light-fastness.
According to a first aspect of the present invention there is provided a composition comprising a compound of Formula (1) and compound of Formula (2) or salts thereof:
wherein the weight ratio of the compound of Formula (1) to the compound of Formula (2) is 1:4 to 1:1.
Preferably the weight ratio of the compound of Formula (1) to the compound of Formula (2) is from 1:3.9 to 1:1, more preferably 1:3.5 to 1:1, especially 1:3 to 1:1.
The dye of Formula (1) is known as C.I.Direct Yellow 86 and may be obtained commercially from a number of sources listed in the colour index, including Avecia Limited.
The Dye of Formula (2) may be prepared by the method described in U.S. Pat. No. 5,268,459, Example 6.
Preferred salts are alkali metal salts, especially lithium, sodium and potassium salts, ammonium and substituted ammonium salts. Especially preferred salts are salts with ammonia, an organic amine or a quaternary amine (e.g.(CH
3
)
4
N
+
). The dyes may be converted into a salt using known techniques. For example, an alkali metal salt of a dye may be converted into a salt with ammonia or an amine by dissolving an alkali metal salt of the dye in water, acidifying with a mineral acid and adjusting the pH of the solution to pH 9 to 9.5 with ammonia or the amine and removing the alkali metal cations by dialysis.
The dyes may exist in tautomeric forms other than those shown in this specification. These tautomers are included within the scope of the present claims.
According to a second aspect of the present invention there is provided a liquid composition comprising a compound of Formula (1), a compound of Formula (2) and a liquid medium. In a preferred aspect this liquid composition comprises:
(a) from 0.01 to 30 parts of a composition comprising a compound of the Formula (1) and a compound of Formula (2); and
(b) from 70 to 99.99 parts of a liquid medium;
wherein all parts are by weight and the number of parts of (a)+(b)=100.
The number of parts of component (a) is preferably from 0.1 to 20, more preferably from 0.5 to 15, and especially from 1 to 5 parts. The number of parts of component (b) is preferably from 99.9 to 80, more preferably from 99.5 to 85, especially from 99 to 95 parts.
The preferred weight ratio of compounds (1) and (2) is as described in relation to the first aspect of the present invention.
Preferably component (a) is completely dissolved in component (b). Preferably component (a) has a solubility in component (b) at 20° C. of at least 10%. This allows the preparation of concentrates which may be used to prepare more dilute inks and reduces the chance of the dye precipitating if evaporation of the liquid medium occurs during storage.
Preferred liquid media include water, a mixture of water and an organic solvent and an organic solvent free from water.
When the liquid medium comprises a mixture of water and an organic solvent, the weight ratio of water to organic solvent is preferably from 99:1 to 1:99, more preferably from 99:1 to 50:50 and especially from 95:5 to 80:20.
It is preferred that the organic solvent present in the mixture of water and organic solvent is a water-miscible organic solvent or a mixture of such solvents. Preferred water-miscible organic solvents include C
1-6
-alkanols, preferably methanol, ethanol, n-propanol, isopropanol, n-butanol, sec-butanol, tert-butanol, n-pentanol, cyclopentanol and cyclohexanol; linear amides, preferably dimethylformamide or dimethylacetamide; ketones and ketone-alcohols, preferably acetone, methyl ether ketone, cyclohexanone and diacetone alcohol; water-miscible ethers, preferably tetrahydrofuran and dioxane; diols, preferably diols having from 2 to 12 carbon atoms, for example pentane-1,5-diol, ethylene glycol, propylene glycol, butylene glycol, pentylene glycol, hexylene glycol and thiodiglycol and oligo- and poly-alkyleneglycols, preferably diethylene glycol, triethylene glycol, polyethylene glycol and polypropylene glycol; triols, preferably glycerol and 1,2,6-hexanetriol; mono-C
1-4
-alkyl ethers of diols, preferably mono-C
1-4
-alkyl ethers of diols having 2 to 12 carbon atoms, especially 2-methoxyethanol, 2-(2-methoxyethoxy)ethanol, 2-(2-ethoxyethoxy)-ethanol, 2-[2-(2-methoxyethoxy)ethoxy]ethanol, 2-[2-(2-ethoxyethoxy)-ethoxy]-ethanol and ethyleneglycol monoallylether; cyclic amides, preferably 2-pyrrolidone, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, caprolactam and 1,3-dimethylimidazolidone; cyclic esters, preferably caprolactone; sulphoxides, preferably dimethyl sulphoxide and sulpholane. Preferably the liquid medium comprises water and 2 or more, especially from 2 to 8, water-soluble organic solvents.
Examples of further suitable ink media comprising a mixture of water and one or more organic solvents are described in U.S. Pat. No. 4,963,189, U.S. Pat. No. 4,703,113, U.S. Pat. No. 4,626,284 and EP 4,251,50A.
When the liquid medium comprises an organic solvent free from water, (i.e. less than 1% water by weight) the solvent preferably has a boiling point of from 30° to 200° C., more preferably of from 40° to 150° C., especially from 50 to 125° C. The organic solvent may be water-immiscible, water-miscible or a mixture of such solvents. Preferred water-miscible organic solvents are any of the hereinbefore described water-miscible organic solvents and mixtures thereof. Preferred water-immiscible solvents include, for example, aliphatic hydrocarbons; esters, preferably ethyl acetate; chlorinated hydrocarbons, preferably CH
2
Cl
2
; and ethers, preferably diethyl ether; and mixtures thereof.
When the liquid medium comprises a water-immiscible organic solvent, preferably a polar solvent is included because this enhances solubility of the dye in the liquid medium. Examples of polar solvents include C
1-4
-alcohols. In view of the foregoing preferences it is especially preferred that where the liquid medium is an organic solvent free from water it comprises a ketone (especially methyl ethyl ketone) &/or an alcohol (especially a C
1-4
-alkanol, more especially ethanol or propanol).
The organic solvent free from water may be a single organic solvent or a mixture of two or more organic solvents. It is preferred that when the medium is an organic solvent free from water it is a mixture of 2 to 5 different organic solvents. This allows a medium to be selected which gives good control over the dryin
Presgrave John Edward
Watkinson Janette
Wight Paul
Avecia Limited
Klemanski Helene
Pillsbury & Winthrop LLP
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