Robust method for producing latex seed particles

Patent metadata

Field	Value
Publication number	US-9809698-B2
Application number	US-201514737440-A
Country	US
Kind code	B2
Filing date	Jun 11, 2015
Priority date	Jun 11, 2015
Publication date	Nov 7, 2017
Grant date	Nov 7, 2017

Abstract

A process directed to emulsion polymerization (EP) methods for producing seed particles reproducibly independent of initiator amount and rate of introduction.

First claim

We claim:

1. A method of producing resin seed particles comprising:
(a) combining (i) water, (ii) an amount of a first branched alkyl diphenyl oxide disulfonate, (iii) a monomer, (iv) an optional branching agent and (v) an optional chain transfer agent in a vessel to form a monomer mixture;
(b) combining (i) water and (ii) an amount of a second branched alkyl diphenyl oxide disulfonate in a reactor to form a seed surfactant solution, wherein the amount of the first branched alkyl diphenyl oxide disulfonate in the vessel of step (a) is at least four times greater than the amount of the second branched alkyl diphenyl oxide disulfonate in the reactor of step (b);
(c) charging an aliquot of said monomer mixture into the reactor containing the seed surfactant solution; and
(d) adding an initiator to said reactor containing the seed surfactant solution and the aliquot of the monomer mixture at an initiator adding rate to obtain resin seed particles,
wherein the initiator adding rate varies by at least 350% during step (d), and further wherein the resin seed particles formed by step (d) are characterized by a D50 size and a deviation of the D50 size of no more than ±3 nm.

2. The method of claim 1 , wherein the resin of said resin seed particles comprises poly(styrene-alkyl acrylate), poly(styrene-1,3-diene), poly(styrene-alkyl methacrylate), poly(styrene-alkyl acrylate-acrylic acid), poly(styrene-1,3-diene-acrylic acid), poly(styrene-alkyl methacrylate-acrylic acid), poly(alkyl methacrylate-alkyl acrylate), poly(alkyl methacrylate-aryl acrylate), poly(aryl methacrylate-alkyl acrylate), poly(alkyl methacrylate-acrylic acid), poly(styrene-alkyl acrylate-acrylonitrile-acrylic acid), poly(styrene-1,3-diene-acrylonitrile-acrylic acid), poly(alkyl acrylate-acrylonitrile-acrylic acid, poly(methyl styrene-butadiene), poly(methyl methacrylate-butadiene), poly(ethyl methacrylate-butadiene), poly(propyl methacrylate-butadiene), poly(butyl methacrylate-butadiene), poly(methyl acrylate-butadiene), poly(ethyl acrylate-butadiene), poly(propyl acrylate-butadiene), poly(butyl acrylate-butadiene), poly(styrene-isoprene), poly(methyl styrene-isoprene), poly(methyl methacrylate-isoprene), poly(ethyl methacrylate-isoprene), poly(propyl methacrylate-isoprene), poly(butyl methacrylate-isoprene), poly(methyl acrylate-isoprene), poly(ethyl acrylate-isoprene), poly(propyl acrylate-isoprene), poly(butyl acrylate-isoprene), poly(styrene-propyl acrylate), poly(styrene-butyl acrylate), poly(styrene-butadiene-acrylic acid), poly(styrene-butadiene-methacrylic acid), poly(styrene-butadiene-acrylonitrile-acrylic acid), poly(styrene-butyl acrylate-acrylic acid), poly(styrene-butyl acrylate-methacrylic acid), poly(styrene-butyl acrylate-acrylonitrile), poly(styrene-butyl acrylate-acrylonitrile-acrylic acid) or combinations thereof.

3. The method of claim 1 , wherein said initiator is selected from the group consisting of potassium persulfate, ammonium persulfate (APS), sodium persulfate, 2,2′-azobis[2-(2-imidazolin-2-yl)propane]dihydrochloride, 2,2′-azobis[2-(2-imidazolin-2-yl)propane]disulfate dehydrate, 2,2′-azobis[2-[1-(2-hydroxyethyl)-2-imidazolin-2-yl]propane]dihydrochloride, 2,2′-azobis[2-(2-imidazolin-2-yl)propane], 2,2′-azobis(1-imino-1-pyrrolidino-2-ethylpropane)dihydrochloride, 2,2′-azobis[2-methyl-N-(2-hydroxyethyl)propionamide] and combinations thereof.

4. The method of claim 1 , wherein said first and second branched alkyl diphenyl oxide disulfonates are each a branched dodecyl diphenyl oxide disulfonate.

5. The method of claim 4 , wherein a ratio of the amount of the second branched alkyl diphenyl oxide disulfonate in the reactor to the amount of the first branched alkyl diphenyl oxide disulfonate in the vessel is in the range of from 20:80 to 17:82.

6. The method of claim 5 , wherein said monomer mixture comprises a styrene and an acrylate.

7. The method of claim 6 , wherein the ratio is 18:82.

8. The method of claim 1 , wherein the resin of said resin seed particles comprises a polyester polymer.

9. The method of claim 1 , further comprising incubating additional monomer with said resin seed particles formed by step (d) to obtain resin particles greater than about 100 nm in size.

10. The method of claim 1 , wherein said first and second branched alkyl diphenyl oxide disulfonates are the same.

11. The method of claim 1 , wherein said monomer mixture comprises decanediol diacrylate.

12. The method of claim 1 , wherein said monomer mixture comprises dodecanethiol.

13. The method of claim 1 , wherein said monomer mixture comprises a styrene and an acrylate.

14. The method of claim 1 , wherein a ratio of the amount of the second branched alkyl diphenyl oxide disulfonate in the reactor to the amount of the first branched alkyl diphenyl oxide disulfonate in the vessel is in the range of from 20:80 to 17:82.

15. The method of claim 14 , wherein the ratio is about 18:82.

16. The method of claim 1 , wherein the initiator adding rate varies by at least 400% during step (d).

17. The method of claim 16 , wherein the D50 size is less than 70 nm.

18. A method of making a toner comprising the method of claim 1 and further comprising
(e) incubating additional monomer with said resin seed particles formed by step (d) to obtain resin particles;
(f) aggregating the resin particles to form aggregated particles;
(g) coalescing said aggregated particles to form toner particles; and
(h) isolating the toner particles from step (g).

19. The method of claim 18 , further comprising adding a shell to the aggregated particles of step (f).

Assignees

• Xerox Corp

Inventors

• Li Shigeng
• Zuo Yanjia
• Cheng Chieh-Min

Classifications

• G03G9/0817 Primary

  Separation; Classifying · CPC title

• C08K5/42 Primary

  Sulfonic acids; Derivatives thereof · CPC title