Ultraviolet-curable liquid developer
US-2016349653-A1 · Dec 1, 2016 · US
US9547248B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9547248-B2 |
| Application number | US-201414177650-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 11, 2014 |
| Priority date | Apr 26, 2012 |
| Publication date | Jan 17, 2017 |
| Grant date | Jan 17, 2017 |
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A method of manufacturing a liquid electrophotographic ink includes: mixing a pigment with a resin powder; and microfluidizing the mixture together with a carrier fluid in a microfluidizer in a number of passes to form a concentrated ink containing composite particles.
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What is claimed is: 1. A method of manufacturing a liquid electrophotographic ink including: mixing a pigment with a resin powder; and without melting the resin powder mixed with the pigment, microfluidizing the mixture together with a carrier fluid in a microfluidizer in a number of passes to form a concentrated ink containing composite particles wherein the composite particles comprise pigments attached to resin particles. 2. The method of claim 1 wherein the pigment is a yellow pigment selected from the group consisting of C.I. Pigment Yellow 1, C.I. Pigment Yellow 2, C.I. Pigment Yellow 3, C.I. Pigment Yellow 4, C.I. Pigment Yellow 5, C.I. Pigment Yellow 6, C.I. Pigment Yellow 7, C.I. Pigment Yellow 10, C.I. Pigment Yellow 11, C.I. Pigment Yellow 12, C.I. Pigment Yellow 13, C.I. Pigment Yellow 14, C.I. Pigment Yellow 16, C.I. Pigment Yellow 17, C.I. Pigment Yellow 24, C.I. Pigment Yellow 34, C.I. Pigment Yellow 35, C.I. Pigment Yellow 37, C.I. Pigment Yellow 53, C.I. Pigment Yellow 55, C.I. Pigment Yellow 65, C.I. Pigment Yellow 73, C.I. Pigment Yellow 74, C.I. Pigment Yellow 75, C.I. Pigment Yellow 81, C.I. Pigment Yellow 83, C.I. Pigment Yellow 93, C.I. Pigment Yellow 94, C.I. Pigment Yellow 95, C.I. Pigment Yellow 97, C.I. Pigment Yellow 98, C.I. Pigment Yellow 99, C.I. Pigment Yellow 108, C.I. Pigment Yellow 109, C.I. Pigment Yellow 110, C.I. Pigment Yellow 113, C.I. Pigment Yellow 114, C.I. Pigment Yellow 117, C.I. Pigment Yellow 120, C.I. Pigment Yellow 124, C.I. Pigment Yellow 128, C.I. Pigment Yellow 129, C.I. Pigment Yellow 133, C.I. Pigment Yellow 138, C.I. Pigment Yellow 139, C.I. Pigment Yellow 147, C.I. Pigment Yellow 151, C.I. Pigment Yellow 153, C.I. Pigment Yellow 154, Pigment Yellow 155, C.I. Pigment Yellow 167, C.I. Pigment Yellow 172, and C.I. Pigment Yellow 180. 3. The method of claim 2 wherein a mixture of two pigments is employed. 4. The method of claim 1 wherein the resin is selected from the group consisting of ethylene acid copolymers and ethylene vinyl acetate copolymers. 5. The method of claim 1 wherein the microfluidizer uses a 60 to 500 μm nozzle auxiliary and interaction chamber with a pressure at the nozzle of about 1,000 to 25,000 psi. 6. The method of claim 1 wherein the carrier fluid is selected from the group consisting of aliphatic hydrocarbons, including substituted or unsubstituted, linear or branched, aliphatic compounds, as well as aliphatic hydrocarbons with aryl substituents. 7. The method of claim 6 wherein the aliphatic hydrocarbons are selected from the group consisting of paraffins, isoparaffins, oils, alkanes having from about 6 to about 100 carbon atoms, and mixtures thereof. 8. The method of claim 1 wherein the number of passes is three. 9. The method of claim 1 wherein the composite particles have a particle size ranging from about 1 to 10 μm. 10. The method of claim 1 , further comprising maintaining the mixture at a temperature from about 5° C. to about 20° C. during the microfluidizing. 11. The method of claim 1 , wherein the pigment is a yellow pigment and the concentrated ink contains from 21-28% non-volatile solids.
in liquid developer mixtures · CPC title
characterised by the liquid · CPC title
characterised by the colouring agents · CPC title
obtained by reactions only involving carbon-to-carbon unsaturated bonds · CPC title
Developers not provided for in groups G03G9/06 - G03G9/135, e.g. solutions, aerosols · CPC title
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