Polymer coated toner pigments for electrophotographic printing

Patent metadata

Field	Value
Publication number	US-9423709-B2
Application number	US-74155010-A
Country	US
Kind code	B2
Filing date	Nov 30, 2007
Priority date	Nov 30, 2007
Publication date	Aug 23, 2016
Grant date	Aug 23, 2016

Abstract

Toner compositions for electrophotographic printing are disclosed, along with methods for making such toners, and printing systems utilizing them. The disclosed process imparts qualities to the toner making it more efficiently and effectively incorporated into printed images.

First claim

What is claimed is:

1. A method of making a toner for use in electrophotographic printing, comprising:
(a) dispersing pigment particles, acrylic monomer, acidic monomer, an initiator, and optionally a charge control agent together in a first solvent so as to create a dispersion;
(b) activating the initiator; and
(c) conducting polymerization of the acrylic monomer and the acidic monomer to form a polymer, where the polymer precipitates out of solution to create a polymer coating on the pigment particles, wherein each pigment particle is at least substantially covered by the polymer coating, the polymer coating is non-crosslinked and has a Tg of from about 20° C. to about 160° C., and each pigment particle is uniformly chargeable over its entire surface.

2. The method of claim 1 , comprising the further step of adding to the dispersion a second solvent in which the polymer has a lower solubility than in the first solvent.

3. The method of claim 1 , wherein the dispersing step is accomplished by milling.

4. The method of claim 1 , wherein the initiator is a thermal initiator and the activating step is accomplished by heating.

5. The method of claim 1 , wherein the initiator is a photo initiator and the activating step is accomplished by exposing to light.

6. The method of claim 1 , wherein the acrylic monomer is selected from the group consisting of: methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, hexyl methacrylate, octyl methacrylate, lauryl methacrylate, octadecyl methacrylate, ethylhexyl methacrylate, isobutyl methacrylate, cyclohexyl methacrylate, stearyl methacrylate, methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, hexyl acrylate, octyl acrylate, lauryl acrylate, octadecyl acrylate, ethylhexyl acrylate, isobutyl acrylate, styrene, alpha-methyl styrene, p-methyl styrene, vinylbenzyl chloride, vinyl acetate, vinyl benzoate, ethylene glycol monomethacrylate with ethylene oxide units from 1 to 100, vinyl ethers, maleimide derivatives, and combinations thereof.

7. The method of claim 1 , wherein the acidic monomers are selected from the group consisting of: acrylic acid, methacrylic acid, itaconic acid, maleic acid, methacryloyloxyethyl succinate, styrene sulfonic acid, allyl sulfonic acid, vinyl benzoic acid, and combinations thereof.

8. The method of claim 1 , wherein the acrylic monomer is selected, along with other components, so as to impart to the polymer coating a Tg of from about 50° C. to about 80° C.

Assignees

• Ganapathiappan Sivapackia
• Bhattacharyya Manoj K
• Ng Hou T
• Hewlett Packard Development Co Lp

Inventors

• Ganapathiappan Sivapackia
• Bhattacharyya Manoj K
• Ng Hou T

Classifications

• G03G9/08726

  Polymers of unsaturated acids or derivatives thereof · CPC title

• G03G9/08795

  characterised by their chemical properties, e.g. acidity, molecular weight, sensitivity to reactants · CPC title

• G03G9/0806 Primary

  whereby chemical synthesis of at least one of the toner components takes place · CPC title

• G03G9/08797

  characterised by their physical properties, e.g. viscosity, solubility, melting temperature, softening temperature, glass transition temperature · CPC title

• C09C1/56

  Treatment of carbon black {; Purification} · CPC title