Composite particles for toner additives
US-2024417537-A1 · Dec 19, 2024 · US
US2016333185A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016333185-A1 |
| Application number | US-201615224964-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 1, 2016 |
| Priority date | Nov 5, 2010 |
| Publication date | Nov 17, 2016 |
| Grant date | — |
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The present invention is directed to methods of making an electrophoretic dispersion comprising pigment particles dispersed in a solvent or solvent mixture, wherein said pigment particles comprises at least one polymer chain comprising a terminal thiocarbonylthio group, attached to the particle surface. The invention also relates to pigment particles suitable for use in an electrophoretic dispersion and methods for their preparation through a RAFT polymerization technique.
Opening claim text (preview).
What is claimed is: 1 . A method of preparing pigment particles comprising polymer chains attached to the pigment particle surface, comprising: (a) reacting pigment particles with a Reversible Addition-Fragmentation chain Transfer (RAFT) reagent bearing an anchoring group; and (b) performing RAFT polymerization in the presence of a free radical initiator, thereby causing the pigment particles to attach to polymer chains comprising: an outer polymer layer formed from first monomers, the outer polymer layer being compatible with a hydrocarbon solvent, an inner polymer layer formed from second monomers different from the first monomers, wherein the second monomers comprise a charged functional group to provide charge to the pigment particles, and a terminal thiocarbonylthio group attached to the outer polymer layer. 2 . The method of claim 1 , wherein the terminal thiocarbonylthio group comprises an optionally substituted alkyl, an optionally substituted aryl, an optionally substituted alkylaryl, or an optionally substituted arylalkyl group. 3 . The method of claim 1 , wherein the first monomer is selected from the group consisting of styrene, methyl acrylate, methyl methacrylate, n-butyl acrylate, n-butyl methacrylate, t-butyl acrylate, t-butyl methacrylate, vinyl pyridine, n-vinyl pyrrolidone, 2-hydoxyethyl acrylate, 2-hydroxyethyl methacrylate, dimethylaminoethyl methacrylate, vinylbenzylaminoethylaminopropyl-trimethoxysilane, methacryloxypropyltrimethoxysilane, acrylic acid, methacrylic acid and vinyl phosphoric acid, and the second monomer is selected from the group consisting of lauryl acrylate, lauryl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, hexyl acrylate, hexyl methacrylate, n-octyl acrylate, n-octyl methacrylate, n-octadecyl acrylate, and n-octadecyl methacrylate. 4 . The method of claim 1 , further comprising mixing the pigment particles with a reagent comprising both the free radical initiator and the anchoring group. 5 . The method of claim 1 , wherein steps (a) and (b) are initiated with different free radical initiators. 6 . The method of claim 1 , further comprising modifying the surface of the pigment particles to introduce a vinyl functional group. 7 . The method of claim 1 , wherein the resulting particle comprises a molar ratio of first monomers to second monomers of between 10:1 and 1:1. 8 . The method of claim 1 , wherein the anchoring group is a carboxylic acid group, a primary amino group, a secondary amino group, a hydroxyl group, a mecapto group, or a silane group.
characterised by the composition or particle type · CPC title
Treatment of carbon black {; Purification} · CPC title
by electrophoresis · CPC title
Macromolecular compounds obtained by polymerising monomers on to inorganic materials · CPC title
Treatment with macro-molecular organic compounds · CPC title
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