Additive attachment on toner particles by plasma
US-9223237-B2 · Dec 29, 2015 · US
US9958797B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-9958797-B1 |
| Application number | US-201715444408-A |
| Country | US |
| Kind code | B1 |
| Filing date | Feb 28, 2017 |
| Priority date | Feb 28, 2017 |
| Publication date | May 1, 2018 |
| Grant date | May 1, 2018 |
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A toner process comprising (a) providing at least one amphiphilic block copolymer prepared by surfactant-free emulsion polymerization comprising: dissolving a hydrophilic monomer in water; adding a hydrophobic monomer; adding a feed initiator to produce a colloidal dispersion of amphiphilic block copolymer; and optionally, discharging the amphiphilic block copolymer; (b) contacting one or more of a latex polymer, a wax; and a colorant with the colloidal dispersion of amphiphilic block copolymer to form a blend; or contacting the discharged amphiphilic block copolymer with one or more of a latex polymer, a wax dispersion, and a colorant dispersion, and forming a further dispersion; (c) heating the blend or further dispersion at a temperature below the glass transition temperature of the latex polymer to form aggregated toner particles; (d) adding a coalescing agent to the toner particles thereby coalescing the toner particles; and (e) recovering the toner particles.
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The invention claimed is: 1. A toner process comprising: (a) providing at least one amphiphilic block copolymer, wherein the amphiphilic block copolymer is prepared by surfactant-free emulsion polymerization comprising: dissolving at least one hydrophilic monomer in water; adding at least one hydrophobic monomer; optionally, adding a feed initiator; optionally, heating; to produce a colloidal dispersion of amphiphilic block copolymer; optionally, cooling; and optionally, discharging the produced colloidal dispersion of amphiphilic block copolymer; (b) contacting one or more components selected from the group consisting of a latex polymer, a wax; and a colorant with the colloidal dispersion of amphiphilic block copolymer to form a blend; or contacting the discharged amphiphilic block copolymer with one or more latexes or dispersions selected from the group consisting of a latex polymer, a polymer dispersion, a wax dispersion, and a colorant dispersion, and forming a dispersion; (c) heating the blend or dispersion at a temperature below the glass transition temperature of the latex polymer to form aggregated toner particles; (d) adding a coalescing agent to the toner particles thereby coalescing the toner particles; and (e) optionally, recovering the toner particles. 2. The toner process of claim 1 , wherein dissolving at least one hydrophilic monomer in water comprises dissolving the at least one hydrophilic monomer in water under agitation. 3. The toner process of claim 1 , wherein the feed initiator is added continuously at a rate of from about 10 −4 mM/minute to about 1 M/minute. 4. The toner process of claim 1 , wherein the amphiphilic block copolymer produced in step (a) comprises homopolymer blocks and wherein the amphiphilic block copolymer has at least two distinct glass transition temperatures corresponding to the glass transition temperature of each homopolymer. 5. The toner process of claim 1 , wherein the amphiphilic block copolymer produced in step (a) comprises hydrophobic chain segments and hydrophilic chain segments in different chain blocks. 6. The toner process of claim 1 , wherein the amphiphilic block copolymer produced in step (a) comprises a molecular weight of from about 5,000 g/mol to about 5×10 6 g/mol. 7. The toner process of claim 1 , wherein the at least one hydrophilic monomer is selected from the group consisting of β-carboxyethyl acrylate, methacrylic acid, sodium 4-vinylbenzenesulfonate, 2-sulfoethyl methacrylate, 4-vinylbenzoic acid, sodium acrylate, 3-sulfopropyl methacrylate sodium salt, 3-sulfopropyl methacrylate potassium salt, N,N-diethylacrylamide, N,N-dimethylacrylamide, 2-(N,N-diethylamino)ethyl methacrylate, 2-(N,N-dimethylamino)ethyl acrylate, N-(2-aminoethyl) methacrylamide hydrochloride, 2-acryloxyethyltrimethylammonium chloride, N-(2-aminoethyl) methacrylamide hydrochloride, methacryloyl-L-Lysine, and combinations thereof. 8. The toner process of claim 1 , wherein the at least one hydrophobic monomer is selected from the group consisting of styrene, alkyl acrylates, alkyl methacrylates, benzyl methacrylates, 2-phenoxyethyl methacrylate, and combinations thereof. 9. The toner process of claim 1 , wherein the feed initiator is selected from the group consisting of ammonium persulfate, potassium persulfate, azobisisobutyronitrile, water soluble azo initiators, and combinations thereof. 10. The toner process of claim 1 , further comprising: adding a second latex polymer to the aggregated toner particles to form a shell over the aggregated toner particles thereby forming a core-shell toner; adding the coalescing agent to the toner particles, and subsequently heating the core-shell toner with the coalescing agent at a temperature above the glass transition temperature of the second latex polymer. 11. A toner produced by the process of claim 1 . 12. The toner process of claim 1 , wherein the latex polymer is a polyester. 13. The toner process of claim 1 , wherein the feed initiator is added continuously at a rate of from about 10 −6 mM/minute to about 100 mM/minute. 14. The toner process of claim 1 , wherein the latex polymer is an amorphous polyester, a crystalline polyester, or a mixture thereof. 15. The toner process of claim 1 , wherein the latex polymer is a polymer formed from a monomer selected from the group consisting of styrenes, acrylates, methacrylates, butadienes, isoprenes, acrylic acids, methacrylic acids, acrylonitriles, and combinations thereof.
Block polymers · CPC title
whereby chemical synthesis of at least one of the toner components takes place · CPC title
Preparation thereof · CPC title
characterised by their chemical properties, e.g. acidity, molecular weight, sensitivity to reactants · CPC title
Polymers of esters · CPC title
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