WO1997033943A1 - Hot melt ink composition - Google Patents
Hot melt ink composition Download PDFInfo
- Publication number
- WO1997033943A1 WO1997033943A1 PCT/GB1997/000448 GB9700448W WO9733943A1 WO 1997033943 A1 WO1997033943 A1 WO 1997033943A1 GB 9700448 W GB9700448 W GB 9700448W WO 9733943 A1 WO9733943 A1 WO 9733943A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- weight
- hot melt
- composition
- composition according
- linear primary
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 37
- 239000012943 hotmelt Substances 0.000 title claims abstract description 20
- 150000003138 primary alcohols Chemical class 0.000 claims abstract description 11
- 239000000049 pigment Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000976 ink Substances 0.000 description 29
- 239000004615 ingredient Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 235000006708 antioxidants Nutrition 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000003981 vehicle Substances 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000007641 inkjet printing Methods 0.000 description 3
- 239000003380 propellant Substances 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- DMCJFWXGXUEHFD-UHFFFAOYSA-N pentatriacontan-18-one Chemical compound CCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCCCC DMCJFWXGXUEHFD-UHFFFAOYSA-N 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 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 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003077 lignite Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- DJWFNQUDPJTSAD-UHFFFAOYSA-N n-octadecyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCCCCCCCC DJWFNQUDPJTSAD-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance 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
- C09D11/34—Hot-melt inks
Definitions
- the present invention relates to a composition suitable for use in the field of hot melt ink-jet printing.
- Hot melt inks for use in ink-jet printing are compositions in which a dye or pigment is admixed with a vehicle which is essentially solid at room temperature but liquid at an elevated temperature at which print heads operate.
- the main advantage of hot melt inks over ink-jet inks which are liquids at room temperature, is that they solidify rapidly upon contact with the substrate, thus giving a print quality which is essentially independent of the nature of the substrate.
- independent temperature control of the substrate allows control of droplet spreading, again essentially independent of the properties of the substrate. This enables a superior print quality to be achieved than is obtainable with the liquid inks.
- Ink-jet printing systems can broadly be classified into continuous and drop-on-demand systems. The latter are generally simpler because droplets are ejected by the print heads only when required and no complex apparatus is required for droplet deflection and ink recycling as is necessitated by the continuous systems.
- a common type of drop-on- demand system employs piezoelectric print heads.
- hot-melt inks used in the latter kind of apparatus have until now been capable only of relatively slow printing speeds, due to the relatively high viscosities of known ink compositions intended for this purpose.
- Bubble jet systems are generally intolerant of variations in ink composition, leading to problems of kogation. They also have inferior head-life. Therefore, a need still exists to provide a hot melt ink which is capable of high-speed printing with the piezoelectric kind of print head.
- EP-A-176 228 discloses hot melt ink jet compositions optionally comprising up to 30% by weight of C 14 -C ⁇ 9 alcohols.
- a thermal ink jet composition comprising 15% by weight of neopentyl alcohol is disclosed in EP-A-508 153.
- WO 91/18065 discloses use of linear alcohols of MW 500-1000 as transparentizing agents in hot melt inks. Transparentizing agents are said to be usable at from 2% to 50% by weight. The linear alcohols are used at 9% by weight.
- US-A-5 350 446 discloses Ct g -C 24 alcohols as optional ingredients of hot melt ink jet inks. These are said to be usable at from 50% to 99.1%, preferably from 90% to 99% by weight of the composition but no examples of such compositions are given.
- the present invention now provides a substantially non-aqueous hot melt ink composition
- a substantially non-aqueous hot melt ink composition comprising more than 40% by weight and less than 75% by weight of a linear primary alcohol having an average molecular weight of at least 300, the composition having a viscosity of less than 15 centipoise at 125°C.
- the amount of the linear primary alcohol in the composition is at least 45%, more preferably at least 50% and especially, at least 55% by weight of the total composition.
- the amount of the linear primary alcohol must be less than 75% by weight of the composition, e.g. less than 70% or less than 65% or less than 60%.
- the average molecular weight of the linear primary alcohol incorporated in the composition according to the present invention is preferably from 400 to 750.
- Such alcohols may typically have the general formula (I)
- x has an average value of from 25 to 50.
- Suitable alcohols of this type are obtainable commercially as the Unilin TM range, ex Petrolite Corporation.
- the hot melt ink compositions of the present invention are substantially non-aqueous, that is to say, they contain little or no water. For example, up to 5% by weight of water might be tolerable in such circumstances but preferably, if present at all, the amount of water in the composition is no more than 1%. Of course in practice, if any water is present at all, it will be in infinitesimal quantities, e.g. no more than 0.1% or 0.01% by weight of the total composition.
- Hot melt inks can basically be considered to consist of a fusible carrier plus a colourant (i.e. a soluble dye or dispersed pigment) optionally with minor ingredients such as anti- oxidants.
- a colourant i.e. a soluble dye or dispersed pigment
- the fusible carrier component of the hot melt ink compositions according to the present invention comprise not only the linear primary alcohol but also one or more co-agents.
- the carrier should preferably be relatively hard and non- tacky at ambient temperatures whilst being capable of melting to form inks.
- it has a melting point of at least 65°C.
- a wide variety of materials have been proposed for use as carrier ingredients for hot melt inks.
- any co-agent will in itself be a polymeric substance which is hard at room temperature but which becomes liquid at elevated temperatures.
- Such vehicles are preferably also film-forming polymers at room temperature, e.g. styrene polymers or copolymers, hydrocarbon resins, phenolic resins and fatty acid amides.
- Suitable co-agents are the urethane oligomers described in PCT Patent Specification No. WO 94/14902. These oligomers are the reaction products of diisocyanates with a monohydric alcohol component, optionally followed by another monohydric component or a dihydric alcohol component followed by a monohydric alcohol component.
- Another class of suitable co-agents comprises the urethane- and urea-amides disclosed in our unpublished UK patent application no. 9519646.5. These materials are the reaction products of a mono- or di-isocyanate with one or more functional amides. They typically have molecular weights in the range from 800-1400.
- the fusible carrier as a whole will make up 50-95% by weight, especially 75- 85% by weight of the composition, optionally with one or more with viscosity modifying additives making up the bulk of the remainder and the other optional additives, such as antioxidants, pigments, dyes, etc. in small amounts to make up the balance, e.g. typically less than 10% by weight of the total formulation.
- stearone carnauba wax
- stearyl stearamide hydrogenated castor oil
- erucamide Other materials which may typically be used to modify the viscosity of the fusible carrier are; stearone, carnauba wax, stearyl stearamide, hydrogenated castor oil and erucamide.
- the hot melt ink compositions according to the present invention are vehicles to which a colourant (dye or pigment) and other optional minor ingredients may be added.
- the compositions of the present invention also encompasses inks containing one or more of the aforementioned ingredients.
- the term "colourant” includes materials which endow a non-visible optical properly (e.g. fluorescence) to the ink.
- the colourants are optional ingredients because another way of introducing a colour (or other optical property) is to incorporate a co-agent which itself endows the property, e.g. a polymer or oligomer having a dye moiety bonded onto or incorporated therein. Suitable materials are disclosed in GB-A-2 038 849, US-A-5 264 507, US- 1-5 098 475, EP-A- 540 248 and our unpublished UK patent application no. 9520470.7.
- Suitable dispersants include the isocyanate-modified microcrystalline waxes and lignite waxes described in EP-A-530 295.
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)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU18044/97A AU1804497A (en) | 1996-03-14 | 1997-02-18 | Hot melt ink composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9605399.6 | 1996-03-14 | ||
GBGB9605399.6A GB9605399D0 (en) | 1996-03-14 | 1996-03-14 | Hot melt ink composition |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997033943A1 true WO1997033943A1 (en) | 1997-09-18 |
Family
ID=10790401
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB1997/000448 WO1997033943A1 (en) | 1996-03-14 | 1997-02-18 | Hot melt ink composition |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU1804497A (en) |
GB (1) | GB9605399D0 (en) |
WO (1) | WO1997033943A1 (en) |
Cited By (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6713125B1 (en) | 2002-03-13 | 2004-03-30 | 3D Systems, Inc. | Infiltration of three-dimensional objects formed by solid freeform fabrication |
EP1935950A1 (en) | 2006-12-18 | 2008-06-25 | Xerox Corporation | Phase Change Inks Containing Dialkyl Ethers |
EP1958993A1 (en) | 2007-02-06 | 2008-08-20 | Xerox Corporation | Phase change inks containing colorant compounds |
EP1961793A1 (en) | 2007-02-06 | 2008-08-27 | Xerox Corporation | Phase change inks containing colorant compounds |
EP1961794A1 (en) | 2007-02-06 | 2008-08-27 | Xerox Corporation | Phase change inks containing colorant compounds |
EP2000514A1 (en) | 2007-05-30 | 2008-12-10 | Xerox Corporation | Solid Ink Set Incorporating Naturally Derived Materials and Processes Thereof |
EP2107088A1 (en) | 2008-04-03 | 2009-10-07 | Xerox Corporation | Phase change inks containing Fischer-Tropsch Waxes |
EP2130879A1 (en) | 2008-06-02 | 2009-12-09 | Xerox Corporation | Flush pigment for solid inkjet ink |
US7758268B2 (en) | 2005-12-20 | 2010-07-20 | Xerox Corporation | Hand held photochromic marking implement |
EP2253680A1 (en) | 2009-05-18 | 2010-11-24 | Xerox Corporation | Pigmented phase change inks containing low molecular weight quaternary ammonium salt dispersants |
EP2253611A1 (en) | 2009-05-18 | 2010-11-24 | Xerox Corporation | Low molecular weight quaternary ammonium salt dispersants |
EP2261291A1 (en) | 2009-06-10 | 2010-12-15 | Xerox Corporation | Solid or phase change inks with improved properties |
US8029861B2 (en) | 2008-09-23 | 2011-10-04 | Xerox Corporation | Ink carriers containing low viscosity functionalized waxes, phase change inks including same, and methods for making same |
US8123344B2 (en) | 2008-08-04 | 2012-02-28 | Xerox Corporation | Ink carriers containing surface modified nanoparticles, phase change inks including same, and methods for making same |
US8177897B2 (en) | 2008-11-17 | 2012-05-15 | Xerox Corporation | Phase change inks containing graphene-based carbon allotrope colorants |
US8348409B2 (en) | 2008-11-17 | 2013-01-08 | Xerox Corporation | Ink jet inks containing nanodiamond black colorants |
US8616693B1 (en) | 2012-11-30 | 2013-12-31 | Xerox Corporation | Phase change ink comprising colorants derived from plants and insects |
US8647422B1 (en) | 2012-11-30 | 2014-02-11 | Xerox Corporation | Phase change ink comprising a modified polysaccharide composition |
US8696100B1 (en) | 2012-10-02 | 2014-04-15 | Xerox Corporation | Phase change ink containing synergist for pigment dispersion |
US8714724B2 (en) | 2012-10-02 | 2014-05-06 | Xerox Corporation | Phase change inks containing novel synergist |
US8911543B2 (en) | 2012-12-18 | 2014-12-16 | Xerox Corporation | Phenylcyclohexanol derivatives as wax modifiers and gelators |
US8974047B2 (en) | 2012-11-27 | 2015-03-10 | Xerox Corporation | Phase change ink containing ethylene vinyl acetate |
US9090777B2 (en) | 2013-04-04 | 2015-07-28 | Xerox Corporation | Low cost process for solid ink using dry flushed pigments |
US9090758B2 (en) | 2012-11-30 | 2015-07-28 | Xerox Corporation | Phase change ink comprising modified naturally-derived colorants |
US9157002B2 (en) | 2013-07-12 | 2015-10-13 | Xerox Corporation | Phase change ink pigment dispersion process |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0176228A1 (en) * | 1984-08-27 | 1986-04-02 | Dataproducts Corporation | Hot melt impulse ink jet ink |
EP0181198A2 (en) * | 1984-11-05 | 1986-05-14 | Dataproducts Corporation | Hot melt impulse ink jet ink |
EP0404493A2 (en) * | 1989-06-22 | 1990-12-27 | Xerox Corporation | Hot melt ink compositions |
US5122187A (en) * | 1989-06-22 | 1992-06-16 | Xerox Corporation | Hot melt ink compositions |
EP0508153A2 (en) * | 1991-04-12 | 1992-10-14 | Hewlett-Packard Company | Solid ink compositions for thermal ink-jet printing having improved printing characteristics |
US5350446A (en) * | 1984-11-05 | 1994-09-27 | Dataproducts Corporation | Hot melt impulse ink jet ink with dispersed solid pigment in a hot melt vehicle |
-
1996
- 1996-03-14 GB GBGB9605399.6A patent/GB9605399D0/en active Pending
-
1997
- 1997-02-18 AU AU18044/97A patent/AU1804497A/en not_active Abandoned
- 1997-02-18 WO PCT/GB1997/000448 patent/WO1997033943A1/en active Application Filing
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0176228A1 (en) * | 1984-08-27 | 1986-04-02 | Dataproducts Corporation | Hot melt impulse ink jet ink |
EP0181198A2 (en) * | 1984-11-05 | 1986-05-14 | Dataproducts Corporation | Hot melt impulse ink jet ink |
US5350446A (en) * | 1984-11-05 | 1994-09-27 | Dataproducts Corporation | Hot melt impulse ink jet ink with dispersed solid pigment in a hot melt vehicle |
EP0404493A2 (en) * | 1989-06-22 | 1990-12-27 | Xerox Corporation | Hot melt ink compositions |
US5006170A (en) * | 1989-06-22 | 1991-04-09 | Xerox Corporation | Hot melt ink compositions |
US5122187A (en) * | 1989-06-22 | 1992-06-16 | Xerox Corporation | Hot melt ink compositions |
EP0508153A2 (en) * | 1991-04-12 | 1992-10-14 | Hewlett-Packard Company | Solid ink compositions for thermal ink-jet printing having improved printing characteristics |
Cited By (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6713125B1 (en) | 2002-03-13 | 2004-03-30 | 3D Systems, Inc. | Infiltration of three-dimensional objects formed by solid freeform fabrication |
US7758268B2 (en) | 2005-12-20 | 2010-07-20 | Xerox Corporation | Hand held photochromic marking implement |
EP1935950A1 (en) | 2006-12-18 | 2008-06-25 | Xerox Corporation | Phase Change Inks Containing Dialkyl Ethers |
US7736426B2 (en) | 2007-02-06 | 2010-06-15 | Xerox Corporation | Phase change inks containing colorant compounds |
EP1961794A1 (en) | 2007-02-06 | 2008-08-27 | Xerox Corporation | Phase change inks containing colorant compounds |
EP1961793A1 (en) | 2007-02-06 | 2008-08-27 | Xerox Corporation | Phase change inks containing colorant compounds |
EP1958993A1 (en) | 2007-02-06 | 2008-08-20 | Xerox Corporation | Phase change inks containing colorant compounds |
US8163074B2 (en) | 2007-02-06 | 2012-04-24 | Xerox Corporation | Phase change inks containing colorant compounds |
EP2000514A1 (en) | 2007-05-30 | 2008-12-10 | Xerox Corporation | Solid Ink Set Incorporating Naturally Derived Materials and Processes Thereof |
US7677713B2 (en) | 2007-05-30 | 2010-03-16 | Xerox Corporation | Solid ink set incorporating naturally derived materials and processes thereof |
EP2107088A1 (en) | 2008-04-03 | 2009-10-07 | Xerox Corporation | Phase change inks containing Fischer-Tropsch Waxes |
EP2130879A1 (en) | 2008-06-02 | 2009-12-09 | Xerox Corporation | Flush pigment for solid inkjet ink |
US8123344B2 (en) | 2008-08-04 | 2012-02-28 | Xerox Corporation | Ink carriers containing surface modified nanoparticles, phase change inks including same, and methods for making same |
US8029861B2 (en) | 2008-09-23 | 2011-10-04 | Xerox Corporation | Ink carriers containing low viscosity functionalized waxes, phase change inks including same, and methods for making same |
US8348409B2 (en) | 2008-11-17 | 2013-01-08 | Xerox Corporation | Ink jet inks containing nanodiamond black colorants |
US8177897B2 (en) | 2008-11-17 | 2012-05-15 | Xerox Corporation | Phase change inks containing graphene-based carbon allotrope colorants |
US8101801B2 (en) | 2009-05-18 | 2012-01-24 | Xerox Corporation | Low molecular weight quaternary ammonium salt dispersants |
US8118922B2 (en) | 2009-05-18 | 2012-02-21 | Xerox Corporation | Pigmented phase change inks containing low molecular weight quaternary ammonium salt dispersants |
EP2253611A1 (en) | 2009-05-18 | 2010-11-24 | Xerox Corporation | Low molecular weight quaternary ammonium salt dispersants |
EP2253680A1 (en) | 2009-05-18 | 2010-11-24 | Xerox Corporation | Pigmented phase change inks containing low molecular weight quaternary ammonium salt dispersants |
US8915993B2 (en) | 2009-06-10 | 2014-12-23 | Xerox Corporation | Solid or phase change inks with improved properties |
EP2261291A1 (en) | 2009-06-10 | 2010-12-15 | Xerox Corporation | Solid or phase change inks with improved properties |
US8696100B1 (en) | 2012-10-02 | 2014-04-15 | Xerox Corporation | Phase change ink containing synergist for pigment dispersion |
US8714724B2 (en) | 2012-10-02 | 2014-05-06 | Xerox Corporation | Phase change inks containing novel synergist |
US8974047B2 (en) | 2012-11-27 | 2015-03-10 | Xerox Corporation | Phase change ink containing ethylene vinyl acetate |
US8616693B1 (en) | 2012-11-30 | 2013-12-31 | Xerox Corporation | Phase change ink comprising colorants derived from plants and insects |
US8647422B1 (en) | 2012-11-30 | 2014-02-11 | Xerox Corporation | Phase change ink comprising a modified polysaccharide composition |
US9090758B2 (en) | 2012-11-30 | 2015-07-28 | Xerox Corporation | Phase change ink comprising modified naturally-derived colorants |
US8911543B2 (en) | 2012-12-18 | 2014-12-16 | Xerox Corporation | Phenylcyclohexanol derivatives as wax modifiers and gelators |
US9090777B2 (en) | 2013-04-04 | 2015-07-28 | Xerox Corporation | Low cost process for solid ink using dry flushed pigments |
US9157002B2 (en) | 2013-07-12 | 2015-10-13 | Xerox Corporation | Phase change ink pigment dispersion process |
Also Published As
Publication number | Publication date |
---|---|
GB9605399D0 (en) | 1996-05-15 |
AU1804497A (en) | 1997-10-01 |
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