GB2314561A - Jet inks - Google Patents
Jet inks Download PDFInfo
- Publication number
- GB2314561A GB2314561A GB9613244A GB9613244A GB2314561A GB 2314561 A GB2314561 A GB 2314561A GB 9613244 A GB9613244 A GB 9613244A GB 9613244 A GB9613244 A GB 9613244A GB 2314561 A GB2314561 A GB 2314561A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ink jet
- ink
- pigment
- castor oil
- aqueous ink
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000000976 ink Substances 0.000 title description 65
- 239000000049 pigment Substances 0.000 claims abstract description 42
- -1 poly(ethylene) Polymers 0.000 claims abstract description 27
- 239000004359 castor oil Substances 0.000 claims abstract description 21
- 235000019438 castor oil Nutrition 0.000 claims abstract description 20
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims abstract description 20
- 239000006184 cosolvent Substances 0.000 claims abstract description 13
- 239000008365 aqueous carrier Substances 0.000 claims abstract description 8
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 23
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 13
- 239000000654 additive Substances 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 239000003139 biocide Substances 0.000 claims description 2
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 2
- 230000003115 biocidal effect Effects 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 239000006185 dispersion Substances 0.000 description 9
- 229920001223 polyethylene glycol Polymers 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
- 238000007641 inkjet printing Methods 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 235000001892 vitamin D2 Nutrition 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 2
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- DPJCXCZTLWNFOH-UHFFFAOYSA-N 2-nitroaniline Chemical compound NC1=CC=CC=C1[N+]([O-])=O DPJCXCZTLWNFOH-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- BDNXUVOJBGHQFD-UHFFFAOYSA-N cyclooctane-1,5-diol Chemical compound OC1CCCC(O)CCC1 BDNXUVOJBGHQFD-UHFFFAOYSA-N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- 229950006389 thiodiglycol Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/324—Inkjet printing inks characterised by colouring agents containing carbon black
- C09D11/326—Inkjet printing inks characterised by colouring agents containing carbon black characterised by the pigment dispersant
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
Abstract
A aqueous jet ink comprises essentially: a) an aqueous carrier medium, b) a pigment and c) a hydrogenated castor oil poly(ethylene)oxide condensate Preferably an organic cosolvent is also present.
Description
Field of the Invention
This invention relates to aqueous inks for ink jet printers, and, more particularly to aqueous, pigmented inks which contain a hydrogenated castor oil poly(ethylene oxide) condensate.
Background of the Invention
Ink jet printing is a non-impact method that in response to a digital signal produces droplets of ink that are deposited on a substrate such as paper or transparent film. Ink jet printers, especially thermal or bubble jet drop-on-demand printers have found broad application as output for personal computers in the office and the home.
A major concern with all ink jet printing devices is pluggage of nozzles during peration-and between operations. A critical measured property for an ink jet ink is the "decap time" which is the length of time over which an ink remains fluid in a pen opening when exposed to air and therefore capable of firing a drop of ink at its intended target. "Decap" means the pen is uncovered or "decapped". The major cause of decap failure is due to evaporation of the aqueous carrier medium, i.e., either cosolvent or water. Initial evaporation generally causes an increase in viscosity which affects the ability of the nozzle to fire a drop since ink jet pens are designed to operate within specific viscosity ranges. Initial failure may be a displacement from the intended target position caused by deflection of the drop or creation of an altered trajectory. Continued evaporation may result in a solid component being precipitated or crystallised in the nozzle which in turn could result in an undesirable satellite spray occurring or a single line of print diverging into a double line. Finally, the nozzle may form a solid skin and totally fail by no longer ejecting ink.
Inks for ink-jet use commonly use dyes as colorants. For such inks, it is known that nozzle pluggage can be reduced or eliminated by an addition of a proportion of between 5 and 50%, commonly around 10%, of a relatively involatile organic cosolvent to an aqueous ink.
Various simple aliphatic polyols, such as glycerol, ethylene glycol, propylene glycol, and diethylene glycol are known to be useful for this purpose. In addition, United States Patent 5,169,438 states that cycloaliphatic diols are useful pluggage inhibitors, US Patent 5,173,112 states that various water soluble amides are useful, US Patent 5,205,861 describes the use of heterocyclic diols, and US Patent 5,268,027 describes the use of alkyl bis polyol ethers.
There is interest in using pigments as the colorants for inkjet use, mainly because of the better fastness of prints from such inks towards light and washing. The situation becomes more complicated with such inks, due to the possibility of pigment aggregation or flocculation, and it is not easy, even with the addition of organic cosolvents, to inhibit pluggage efficiently without introducing other disadvantages.
A need therefore exists for a method of inhibiting pluggage for aqueous pigmented inks which does not introduce other disadvantages. We have found that certain poly(ethylene oxide) condensates of hydrogenated castor oil are useful additives for pigmented ink jet inks, which give stable ink formulations with inhibited pluggage.
Summarv of the Invention
The invention relates to an aqueous inkjet ink composition comprising: (a) an aqueous carrier medium, (b) a pigment (c) a hydrogenated castor oil poly(ethylene oxide) condensate
The inks of this invention have superior decap performance, are extremely stable, are rapid drying, have low viscosity, exhibit excellent print quality, and provide excellent water resistance after drying. They may be used with a variety of ink jet printers such as continuous, piezoelectric, drop-on-demand and thermal or bubble jet drop-onaemand, and are particularly adapted for use in thermal inkjet printers.
The inks of this invention are useful for printing on any of the substrates commonly used for ink-jet printing, for example so-called plain paper, coated paper, and transparent film materials.
Detailed Description of the Invention
The invention relates to pigmented ink jet ink compositions which are particularly suited for use in ink jet printers in general, and thermal ink jet printers in particular. The pigmented inks comprise an aqueous carrier medium, a pigment, a poly(ethylene oxide) condensate of hydrogenated castor oil, together with optionally an organic polyol cosolvent together with other components which are advantageously added to aqueous inks, such as surfactants, viscosity modifiers, and biocides. In addition, sequestering agents such as EDTA may also be included to eliminate deleterious effects of heavy metal impurities. Ethoxylated hydrogenated castor oils are well known surfactants. They may be prepared by reduction of castor oil, which is a natural product, and reaction with ethylene oxide. The number in brackets refers to the approximate number of ethylene glycol repeat units per castor oil molecule. Preferably the ethoxylated hydrogenated castor oil comprises appr4ely 40 ethylene glycol repeat units per castor oil molecule.
The term pigment describes a colorant which is essentially insoluble in the aqueous ink medium. Suitable pigments include almost any compound of the types classified as a pigment by the Colour Index, together with certain compounds classified by the Colour Index as vat or disperse dyes. Numerous other insoluble coloured compounds which are not included in the Colour Index are also suitable. Commercially pigments are often supplied as a pigment dispersion, and this invention is useful for pigments supplied as such dispersions, which commonly include dispersants and other cosolvents as well as water.
Preferred specific examples of pigments for a black ink include carbon black (C.I. Pigment
Black 7), such as furnace black, lamp black, acetylene black, and channel black, and o-nitroaniline black (C.I. Pigment Black 1). Preferred specific examples of the pigment for a coloured ink include C.I.Pigment Yellow 1, 3, 12, 13, 14, 17, 24, 34, 35, 37, 53, 55, 81, 83, 95, 97, 98, 100, 101, 104, 108, 109, 110, 117, 120, 138 and 153, C.I. Pigment Orange 5, 13, 16, 17, 36, 43 and 51, C.I. Pigment Red 1, 2, 3, 9, 17, 22, 23, 31, 38, 48:1, 48:2, 48:3, 48:4, 49:1, 52:2, 53:1 and 57:1, 60:1, 63:1, 63:2, 64:1, 81, 83, 88, 104, 105, 106, 112, 114, 122, 123, 146, 149, 166, 168, 170, 172, 177, 178, 179, 184, 188, 190, 193, 209, 219, C.I. Pigment
Violet 1, 3, 5:1, 16, 19, 23, 38, C.I. Pigment Blue 1,2, 15:1, 15:2, 15:3, 15:4, 15:6, 16, 17:1, 56, 60, 63, and C.I. Pigment Green 1, 4, 7, 8, 10, 17, 18, 36. It is also possible to use, besides the above-described pigments, processed pigments such as graft carbon having a surface treated with a resin or the like. It is also possible to mix more than one pigment in the inks of the invention.
The ink may be prepared by dispersing the pigment or predispersed pigment with the hydrogenated castor oil poly(ethylene oxide) condensate and other components in water-wi+ an optional cosolvent.
The dispersing step may be accomplished in a horizontal mini mill, a ball mill, an attritor, or by passing the mixture through a plurality of noales within a liquid jet interaction chamber at a liquid pressure of at least 1000 psi to produce a uniform dispersion of the pigment particles in the aqueous carrier medium.
It is sometimes desirable to make the pigmented ink jet ink in concentrated form, which is subsequently diluted to the appropriate concentration for use in the ink jet printing system.
This technique permits preparation of a greater quantity of pigmented ink from the equipment. If the pigment dispersion is made in a solvent, it is diluted with water and optionally other solvents to obtain the appropriate concentration. If the pigment dispersion is made in water, it is diluted with either additional water or water soluble solvents to make a pigment dispersion of the desired concentration. By dilution, the ink is adjusted to the desired viscosity, colour, hue, saturation density, and print area coverage for the particular application.
The ink may contain up to approximately 30% pigment by weight, but will generally be in the range of approximately 0.1 to 15%, preferably approximately 0.1 to 8%, by weight of the total ink composition for most thermal ink jet printing applications.
The particle diameter of the pigment is preferably 101lm or less, particularly preferably lym or less.
The ink may contain up to 25% of the hydrogenated castor oil poly(ethylene oxide) condensate by weight, but preferably between 3% and 15% by weight, depending on the pigment used and other properties desired of the ink.
The aqueous carrier medium is water or a mixture of water and at least one water soluble organic solvent.
Deionized water is commonly used. Selection of a suitable mixture of water and water soluble organic solvent, depends on the requirements of the specific application, such as the desired surface tension and viscosity, the selected pigment, the drying time of the pigmented ink jet ink, and the type of substrate onto which the ink will be printed.
Representative examples of water-soluble organic solvents that may be selected -include (1) alcohols, such as methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, sec-butyl alcohol, t-butyl alcohol, iso-butyl alcohol, furfuryl alcohol, and tetrahydrofurfuryl alcohol: (2) ketones or ketoalcohols such as acetone, methyl ethyl ketone and diacetone alcohol; (3) ethers, such as tetrahydrofuran and dioxane; (4) esters, such as ethyl lactate, (5) polyhydric alcohols, such as ethylene glycol, diethylenelglycol, triethylene glycol, propylene glycol, tetraethylene glycol, polyethylene glycol, glycerol, 2-methyl-2, 4-pentanediol, 1,2,6-hexanetriol and thiodiglycol; (6) lower alkyl mono-or di-ethers derived from alkylene glycols, such as ethylene glycol monomethyl (or -ethyl) ether, diethylene glycol mono-methyl (or -ethyl) ether, propylene glycol mono-methyl (or -ethyl) ether, triethylene glycol mono-methyl (or -ethyl) ether and diethylene glycol di-methyl (or -ethyl) ether; (7) nitrogen containing organic compounds such as urea, pyrrolidone,
N-methyl-2-pyrrolidone, and 1,3-dimethyl-2-imidazolidinone; and (8) sulfur-containing compounds such as dimethyl sulfoxide and tetramethylene sulfone.
A mixture of water and a water soluble organic solvent having at least 2 hydroxyl groups such as diethylene glycol is preferred as the aqueous carrier medium. It is also possible to use a mixture of water and more than one water soluble organic solvent.
The aqueous composition may contain up to 50% of the organic cosolvent, but preferably up to 10% of each of the organic cosolvents, and most preferably between about 5% and about
10% of the organic cosolvent.
The following examples will serve to illustrate the invention:
Example 1
A commercially available fmely dispersed form of Copper Phthalocyanine (C.I. Pigment blue 15:3) was used. This consists of about 40% raw pigment, and contains a p-n-aikyl phenol ethoxylate as dispersant as well as some propylene glycol. An ink was prepared using the following formulation:
Pigment dispersion 12.5g
Diethylene glycol 5.0g
PEG (40) Hydrogenated Castor Oil 9.0g
Water to make 100g
The mean particle size was 0.45nm measured on a Coulter LS 130.
An HP51626A ink-jet cartridge was filled with this ink and loaded into an HP560 printer.
On jetting, a good quality cyan print was produced. The cartridge was then left overnight.
On jetting, a good quality print was produced immediately, with no evidence of pluggage.
The ink was prepared as follows:
To distilled water, 9g of PEG (40) Hydrogenated castor oil was added, this was stirred magnetically for 10 minutes. To the resultant mixture 5g of Diethylene glycol was added, and stirred for a further five minutes. This fmal mixture was then added to 12.5g of the pigment dispersion and stirred for another 10 minutes.
Example 2
A commercially available finely dispersed form of CI Pigment Red 184 was used, which again contains about 40% raw pigment, alkyl phenol ethoxylate as a dispersant, and propylene glycol. Inks were prepared using the following formulation:
Pigment dispersion 12.5g
Additive 5.0g
Diethylene Glycol l0.0g Water to make 100g Different inks were prepared using the following additives: (Only the ink of the invention comprised the PEG hydrogenated castor oil) a) PEG (40) Hydrogenated castor oil invention b) Polyethylene glycol (PEG 2000) - comparison c) Fatty alcohol ethoxylate - comparison d) PEG (150) lanolin - comparison e) Cis -1, 5 - cyclooctane diol - comparison, see USP 5,159,43Q f) 1,4 - cyclohexane diol - comparison, see USP 5,169,438 g) (no additive) - control
The average particle size of all of these inks measured on the LS130 was 0.20nm. Inks A-G were all individually filled into HP51626A ink-jet cartridges, loaded into'an HP560 printer, and jetted according to a program to give a print of solid colour. All the inks.gavle.a.good colour density, and jetted satisfactorily.
The cartridges were then left overnight. The following day they were again jetted using the same program. In this case, the number of traverses of the print head needed to give an even coverage was counted. For a good ink, this should be zero, or a low number, implying that all the individual jets in the cartridge print immediately with no pluggage. For a bad ink, showing evidence of pluggage, this will be a high number, with a maximum of 58 showing that not all the jets are firing properly even after a full sheet has been printed. The results are given below, showing the advantage of the inventive ink.
Ink Lines for all jets to fire
A - invention 0
B - comparison 17
C comparison > 58
D - comparison > 58
E USP 5,169,438 > 58
F USP 5,169,438 > 58
G - control > 58
This example shows the advantage of the inventive ink, particularly when compared with inks C-G, which effectively blocked all the nozzles of the cartridge on standing.
Example 3
A set of coloured inks was prepared as in example 1, using PEG (40) hydrogenated castor oil as in example 2a. The inks were charged into cartridges and left overnight as in example 2; and the number of lines to give a full print was counted as in example 2. The ink formulation and results are given in the table.
Colour CI Pigments % Diethylene % No. Average Particle Additive Glycol t Pigment lines Size ( m) Cyan Blue 15:3 9 5 3 0 0.4511m Yellow Yellow 13 3 15 3 1 0.12 m Magenta Red 184 9 15 3 1 0.201lm Black Black7 3 5 3 O 0.12m
Claims (7)
- Claims:1. An aqueous ink jet composition which comprises essentially: a) an aqueous carrier medium, b) a pigment andc) a hydrogenated castor oil poly(ethylene)oxide condensate
- 2. An aqueous ink jet composition wherein according to claims the hydrogenated castor oil poly(ethylene) oxide condensate comprises approximately forty ethylene glycol repeat units per castor oil molecule.
- 3. An aqueous ink jet composition according to claim 1 which comprises at least one organic cosolvent.
- 4. An aqueous ink jet composition according to claim 3 wherein the organic cosolvent is diethylene glycol.
- 5. An aqueous ink jet composition according to claim 1 wherein the hydrogenated castor oil poly(ethylene)oxide condensate is present in the composition to the extent of 3 to 15% by weight.
- 6. An aqueous ink jet composition according to claim 3 wherein the amount of organic cosolvent present in the aqueous composition is from 5 to 10% by weight.
- 7. An aqueous ink jet composition according to claim 3 which comprises at least one further additive selected from a surfactant, a solution viscosity modifier and a biocide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9613244A GB2314561B (en) | 1996-06-25 | 1996-06-25 | Aqueous inks for ink jet printers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9613244A GB2314561B (en) | 1996-06-25 | 1996-06-25 | Aqueous inks for ink jet printers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB9613244D0 GB9613244D0 (en) | 1996-08-28 |
| GB2314561A true GB2314561A (en) | 1998-01-07 |
| GB2314561B GB2314561B (en) | 2000-06-07 |
Family
ID=10795816
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB9613244A Expired - Fee Related GB2314561B (en) | 1996-06-25 | 1996-06-25 | Aqueous inks for ink jet printers |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2314561B (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5275647A (en) * | 1991-11-25 | 1994-01-04 | Xerox Corporation | Ink compositions |
-
1996
- 1996-06-25 GB GB9613244A patent/GB2314561B/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5275647A (en) * | 1991-11-25 | 1994-01-04 | Xerox Corporation | Ink compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2314561B (en) | 2000-06-07 |
| GB9613244D0 (en) | 1996-08-28 |
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| 732E | Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977) | ||
| PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20090625 |