Toner manufacture using chain transfer polyesters

• US 5,342,724 A
• Filed: 04/10/1992
• Issued: 08/30/1994
• Est. Priority Date: 04/10/1992
• Status: Expired due to Fees

• Current Assignee: Eastman Kodak Company
• Original Assignee: Eastman Kodak Company
• Inventors: Wilson, John C.
• Primary Examiner(s): Kight, III, John
• Assistant Examiner(s): Dodson, Shelley A.
• Application Number:
  US07/867,307
• Time in Patent Office: 872 Days
• Field of Search: 430/114, 430/115, 430/253, 430/271, 430/273, 430/281, 430/288, 430/907, 430/106.6, 430/107, 430/109, 430/110, 430/111, 525/445
• US Class Current: 430/114
• CPC Class Codes: G03G 9/0806 whereby chemical synthesis of at least one of the toner components takes place
• CPC Class Codes: G03G 9/08755 Polyesters
• CPC Class Codes: G03G 9/08793 Crosslinked polymers
• CPC Class Codes: Y10S 430/108 Polyolefin or halogen containing
• CPC Class Codes: Y10S 430/109 Polyester

Abstract

Polymeric electrophotographic toner and developer compositions are produced by methods including conventional as well as limited coalescence manufacturing techniques. The compositions are prepared by heating a diacid and a diol under conditions effective to form a chain transfer polyester, wherein either the diacid or the diol contain a disulfide moiety. The polyester is reacted with one or more vinyl monomers to form a block copolymer having polyester blocks linked to polyvinyl blocks by sulfide groups previously constituting the disulfide moiety. The block copolymer is reduced to a particulate form to a size suitable for use as an electrophotographic toner by conventional methods, evaporation limited coalescence, and suspension limited coalescence.

Claims

1. A method of making polymeric toner particles comprising the steps of:

heating a diacid and a diol under conditions effective to form a chain transfer polyester, wherein either said diacid or said diol contain a disulfide moiety;

reacting one or more vinyl monomers with said chain transfer polyester in the presence of an initiator under conditions effective to produce a block copolymer having polyester blocks and polyvinyl blocks, wherein said polyester blocks and said polyvinyl blocks are linked together by a sulfide group previously constituting the disulfide moiety; and

reducing said block copolymer to a particulate form to a size suitable for use as an electrographic toner.

2. A method of making polymeric toner particles according to claim 1, wherein the conditions effective to form a chain-transfer polyester comprise heating the diacid and the diol in the presence of a catalyst in an inert atmosphere at about 180°

C. to about 280°

C., and applying a vacuum at about 200°

C. to about 280°

C. to increase the molecular weight of said chain transfer polyester and to remove excess diol.

3. A method of making polymeric toner particles according to claim 1, wherein:

said diacid is chosen from the group consisting of sebacic acid, 1,4-cyclohexanedicarboxylic acid, adipic acid, glutaric acid, succinic acid, carbonic acid, oxalic acid, azelaic acid, 4-cyclohexane-1,2-dicarboxylic acid, 2-ethylsuberic acid, 2,2,3,3-tetramethylsuccinic acid, 4,4'"'"'-bicyclohexyldicarboxylic acid, terephthalic acid, isophthalic acid, dibenzoic acid, bis(p-carboxyphenyl)methane, 2,6-naphthalenedicarboxylic acid, phenanthrene dicarboxylic acid, and 4,4'"'"'-sulfonyldibenzoic acid; and

said diol is chosen from the group consisting of bis(gamma-hydroxypropyl) disulfide, bis(6-hydroxyhexyl) disulfide, bis(6-hydroxy-2-naphthyl) disulfide, bis(4-hydroxyphenyl) disulfide, bis(4-hydroxymethylphenyl) disulfide, bis(2-hydroxymethylphenyl) disulfide, bis(4-(beta-hydroxyethyl)phenyl) disulfide, and bis(3-(beta-hydroxyethyl)phenyl) disulfide.

4. A method of making polymeric toner particles according to claim 1, wherein:

said diacid is chosen from the group consisting of bis(4-carboxyphenyl) disulfide, bis(4-carbomethoxyphenyl) disulfide, 2,2'"'"'-dithio(dibenzoyl chloride), bis(4-chlorocarbonylphenyl) disulfide, dimethyl 4,4'"'"'-dithiodibutyrate, N,N'"'"'-bis(4-carbomethoxybenzoyl)-4,4'"'"'-dithiodianiline, bis(3-carboxyphenyl) disulfide, bis(2-carboxyphenyl) disulfide, 2,3'"'"'-dicarboxydiphenyl disulfide, 2,4'"'"'-dicarboxydiphenyl disulfide, 3,4'"'"'-dicarboxydiphenyl disulfide, bis(4-carboxymethylphenyl) disulfide, bis(3-carboxymethylphenyl) disulfide, bis(2-carboxymethylphenyl) disulfide, bis(10-carboxy-n-decyl) disulfide, 3,3'"'"'-dithiodipropionic acid, N,N'"'"'-bis(beta-carboxypropionyl)-4,4'"'"'-dithiodianiline, N,N'"'"'-bis(gamma-carboxybutyryl)-2,2'"'"'-dithiodianiline, bis(3-carboxy-1-methylpropyl) disulfide, bis(2,3-di-methoxy-6-carboxyphenyl) disulfide, bis(4-carboxy-methoxyphenyl) disulfides and diisocyanate disulfides; and

said diol is chosen from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 2-methyl-1,5-pentanediol, 1,4-cyclohexanedimethanol, 1,4-bis(β

-hydroxyethoxy)cyclohexane, norcamphanediols, 2,2,4,4-tetraalkylcyclobutane-1,3-diols, p-xylene glycol, neopentyl glycol, hydroquinone, 4,4'"'"'-isopropylidenediphenol, and hydroxy-terminated polyesters.

5. A method of making polymeric toner particles according to claim 1, wherein said vinyl monomer is chosen from the group consisting of substituted and unsubstituted styrenes, vinyl naphthalene, ethylenically unsaturated mono-olefins, vinyl halides, vinyl esters, esters of alpha-methylene aliphatic monocarboxylic acids, acrylonitrile, methacrylonitrile, acrylamide, vinyl ethers, vinyl ketones, vinylidene halides, N-vinyl compounds, and mixtures thereof.

6. A method of making polymeric toner particles according to claim 1, further comprising the step of adding a polyfunctional modifier to the diol and the diacid in said heating, wherein said polyfunctional modifier is selected from the group consisting of polyols having three or more hydroxy groups, polycarboxylic acids having three or more carboxylic acid groups, hydroxy acids having three or more total hydroxy and carboxyl groups, and trifunctional and tetrafunctional disulfides.

7. A method of making polymeric toner particles according to claim 1, further comprising the step of adding a crosslinking agent to the vinyl monomer and the chain transfer polyester in said reacting, wherein said crosslinking agent is chosen from the group consisting of aliphatic and aromatic divinyl compounds, diacrylates, dimethacrylates, diacrylamides, and dimethacrylamides.

8. A method of making polymeric toner particles according to claim 1, wherein said initiator is chosen from the group consisting of 2,2'"'"'-azobis(dimethyl valeronitrile), azobisisobutyronitrile, lauroyl peroxide, and azobismethylethylacetonitrile.

9. A method of making polymeric toner particles according to claim 1, wherein said reducing comprises the steps of:

crushing said block copolymer;

melt blending said crushed block copolymer with addenda;

recrushing and coarse grinding said melt blended block copolymer;

pulverizing said recrushed and ground block copolymer to a particulate form to a size suitable for use as an electrographic toner.

10. A method of making polymeric toner particles according to claim 9, wherein said addenda are chosen from the group consisting of colorants and charge-control agents.

11. A method of making polymeric toner particles according to claim 1, further comprising the step of mixing said particulate block copolymer with solid carrier particles to form a two-component developer.

12. A method of making polymeric toner particles according to claim 1, wherein said reducing comprises the steps of:

dissolving said block copolymer in an organic solvent to form an organic phase;

dispersing a stabilizer, a buffering agent, and a promoter in water to form an aqueous phase;

mixing said organic phase with said aqueous phase to form a suspension of small droplets of said organic phase in said aqueous phase; and

removing said solvent from said droplets to form solidified polymeric toner particles.

13. A method of making polymeric toner particles according to claim 12, wherein the conditions effective to form a chain-transfer polyester comprise heating the dicarboxylic acid and the glycol in the presence of a catalyst in an inert atmosphere at about 180°

C. to about 280°

C., and applying a vacuum at about 200°

C. to about 280°

C. to increase the molecular weight of said chain transfer polyester and to remove excess glycol.

14. A method of making polymeric toner particles according to claim 12, wherein:

said diacid is chosen from the group consisting of sebacic acid, 1,4-cyclohexanedicarboxylic acid, adipic acid, glutaric acid, succinic acid, carbonic acid, oxalic acid, azelaic acid, 4-cyclohexane-1,2-dicarboxylic acid, 2-ethylsuberic acid, 2,2,3,3-tetramethylsuccinic acid, 4,4'"'"'-bicyclohexyldicarboxylic acid, terephthalic acid, isophthalic acid, dibenzoic acid, bis(p-carboxyphenyl)methane, 2,6-naphthalenedicarboxylic acid, phenanthrene dicarboxylic acid, and 4,4'"'"'-sulfonyldibenzoic acid; and

said diol is chosen from the group consisting of bis(gamma-hydroxypropyl) disulfide, bis(6-hydroxyhexyl) disulfide, bis(6-hydroxy-2-naphthyl) disulfide, bis(4-hydroxyphenyl) disulfide, bis(4-hydroxymethylphenyl ) disulfide, bis(2-hydroxymethylphenyl ) disulfide, bis(4-(beta-hydroxyethyl) phenyl) disulfide, and bis(3-(beta-hydroxyethyl) phenyl) disulfide.

15. A method of making polymeric toner particles according to claim 12, wherein:

said diacid is chosen from the group consisting of bis(4-carboxyphenyl) disulfide, bis(4-carbomethoxyphenyl) disulfide, 2,2'"'"'-dithio(dibenzoyl chloride), bis(4-chlorocarbonylphenyl) disulfide, dimethyl 4,4'"'"'-dithiodibutyrate, N,N'"'"'-bis(4-carbomethoxybenzoyl)-4,4'"'"'-dithiodianiline, bis(3-carboxyphenyl) disulfide, bis(2-carboxyphenyl) disulfide, 2,3'"'"'-dicarboxydiphenyl disulfide, 2,4'"'"'-dicarboxydiphenyl disulfide, 3,4'"'"'-dicarboxydiphenyl disulfide, bis(4-carboxymethylphenyl) disulfide, bis(3-carboxymethylphenyl) disulfide, bis(2-carboxymethylphenyl) disulfide, bis(10-carboxy-n-decyl) disulfide, 3,3'"'"'-dithiodipropionic acid, N,N'"'"'-bis(beta-carboxypropionyl)-4,4'"'"'-dithiodianiline, N,N'"'"'-bis(gamma-carboxybutyryl)-2,2'"'"'-dithiodianiline, bis(3-carboxy-1-methylpropyl) disulfide, bis(2,3-di-methoxy-6-carboxyphenyl) disulfide, bis(4-carboxy-methoxyphenyl) disulfides and diisocyanate disulfides; and

said diol is chosen from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 2-methyl-1,5-pentanediol, 1,4-cyclohexanedimethanol, 1,4-bis(β

-hydroxyethoxy)cyclohexane, norcamphanediols, 2,2,4,4-tetraalkylcyclobutane-1,3-diols, p-xylene glycol, neopentyl glycol, hydroquinone, 4,4'"'"'-isopropylidenediphenol, and hydroxy-terminated polyesters.

16. A method of making polymeric toner particles according to claim 12, wherein said vinyl monomer is chosen from the group consisting of substituted and unsubstituted styrenes, vinyl naphthalene, ethylenically unsaturated mono-olefins, vinyl halides, vinyl esters, esters of alpha-methylene aliphatic monocarboxylic acids, acrylonitrile, methacrylonitrile, acrylamide, vinyl ethers, vinyl ketones, vinylidene halides, N-vinyl compounds, and mixtures thereof.

17. A method of making polymeric toner particles according to claim 12, further comprising the step of adding a crosslinking agent to the vinyl monomer and the chain transfer polyester in said reacting, wherein said crosslinking agent is chosen from the group consisting of alphatic and aromatic divinyl compounds, diacrylates, dimethacrylates, diacrylamides, and dimethacrylamides.

18. A method of making polymeric toner particles according to claim 12, wherein said initiator is chosen from the group consisting of 2,2'"'"'-azobis(dimethyl valeronitrile), azobisisobutyronitrile, lauroyl peroxide, and azobismethylethylacetonitrile.

19. A method of making polymeric toner particles according to claim 12, wherein said stabilizer is chosen from the group consisting of silica, alumina, barium sulfate, calcium sulfate, barium carbonate, calcium carbonate, calcium phosphate, and latex-based copolymers.

20. A method of making polymeric toner particles according to claim 19, wherein said stabilizer is silica and further comprises the step of separating said silica stabilizer from the surface of said polymeric toner particles.

21. A method of making polymeric toner particles according to claim 12, wherein said promoters are chosen from the group consisting of poly(adipic acid-co-methylaminoethanol) and poly(diethanolamine adipate).

22. A method of making polymeric toner particles according to claim 12, wherein the droplets of the organic phase contain addenda chosen from the group consisting of colorants, and charge control agents.

23. A method of making polymeric toner particles according to claim 12, further comprising the step of mixing said polymeric toner particles with solid carrier particles to form a two component developer.

24. A method of making polymeric toner particles according to claim 1, wherein said reacting and said reducing comprise the steps of:

mixing said chain transfer polyester with a polymerizable vinyl monomer and an initiator to form an organic phase;

dispersing a stabilizer, a buffering agent, and a promoter in water to form an aqueous phase;

mixing said organic phase with said aqueous phase to form a suspension of small droplets of said organic phase in said aqueous phase; and

polymerizing said vinyl monomer with said chain transfer polyester under conditions effective to form particles of a block copolymer having polyester blocks and polyvinyl blocks, wherein said polyester blocks and said polyvinyl blocks are linked together by a sulfide group previously constituting the disulfide moiety.

25. A method of making polymeric toner particles according to claim 24, wherein the conditions effective to form a chain-transfer polyester comprise heating the dicarboxylic acid and the glycol in the presence of a catalyst in an inert atmosphere at about 180°

C. to about 280°

C., and applying a vacuum at about 200°

C. to about 280°

C. to increase the molecular weight of said chain transfer polyester and to remove excess glycol.

26. A method of making polymeric toner particles according to claim 24, wherein:

said diacid is chosen from the group consisting of sebacic acid, 1,4-cyclohexanedicarboxylic acid, adipic acid, glutaric acid, succinic acid, carbonic acid, oxalic acid, azelaic acid, 4-cyclohexane-1,2-dicarboxylic acid, 2-ethylsuberic acid, 2,2,3,3-tetramethylsuccinic acid, 4,4'"'"'-bicyclohexyldicarboxylic acid, terephthalic acid, isophthalic acid, dibenzoic acid, bis(p-carboxyphenyl)methane, 2,6-naphthalenedicarboxylic acid, phenanthrene dicarboxylic acid, and 4,4'"'"'-sulfonyldibenzoic acid; and

said diol is chosen from the group consisting of bis(gamma-hydroxypropyl) disulfide, bis(6-hydroxyhexyl) disulfide, bis(6-hydroxy-2-naphthyl) disulfide, bis(4-hydroxyphenyl) disulfide, bis(4-hydroxymethylphenyl) disulfide, bis(2-hydroxymethylphenyl) disulfide, bis(4-(beta-hydroxyethyl)phenyl) disulfide, bis(3-(beta-hydroxyethyl)phenyl) disulfide.

27. A method of making polymeric toner particles according to claim 24, wherein:

said diacid is chosen from the group consisting of bis(4-carboxyphenyl) disulfide, bis(4-carbomethoxyphenyl) disulfide, 2,2'"'"'-dithio(dibenzoyl chloride), bis(4-chlorocarbonylphenyl) disulfide, dimethyl 4,4'"'"'-dithiodibutyrate, N,N'"'"'-bis(4-carbomethoxybenzoyl)-4,4'"'"'-dithiodianiline, bis(3-carboxyphenyl) disulfide, bis(2-carboxyphenyl) disulfide, 2,3'"'"'-dicarboxydiphenyl disulfide, 2,4'"'"'-dicarboxydiphenyl disulfide, 3,4'"'"'-dicarboxydiphenyl disulfide, bis(4-carboxymethylphenyl) disulfide, bis(3-carboxymethylphenyl) disulfide, bis(2-carboxymethylphenyl) disulfide, bis(10-carboxy-n-decyl) disulfide, 3,3'"'"'-dithiodipropionic acid, N,N'"'"'-bis(beta-carboxypropionyl)-4,4'"'"'-dithiodianiline, N,N'"'"'-bis(gamma-carboxybutyryl)-2,2'"'"'-dithiodianiline, bis(3-carboxy-1-methylpropyl) disulfide, bis(2,3-di-methoxy-6-carboxyphenyl) disulfide, bis(4-carboxy-methoxyphenyl) disulfides and diisocyanate disulfides; and

said diol is chosen from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 2-methyl-1,5-pentanediol, 1,4-cyclohexanedimethanol, 1,4-bis(β

-hydroxyethoxy)cyclohexane, norcamphanediols, 2,2,4,4-tetraalkylcyclobutane-1,3-diols, p-xylene glycol, neopentyl glycol, hydroquinone, 4,4'"'"'-isopropylidenediphenol, and hydroxy-terminated polyesters.

28. A method of making polymeric toner particles according to claim 24, wherein said vinyl monomer is chosen from the group consisting of substituted and unsubstituted styrenes, vinyl naphthalene, ethylenically unsaturated mono-olefins, vinyl halides, vinyl esters, esters of alpha-methylene aliphatic monocarboxylic acids, acrylonitrile, methacrylonitrile, acrylamide, vinyl ethers, vinyl ketones, vinylidene halides, N-vinyl compounds, and mixtures thereof.

29. A method of making polymeric toner particles according to claim 24, further comprising the step of adding a crosslinking agent to the vinyl monomer and the chain transfer polyester in said reacting, wherein said crosslinking agent is chosen from the group consisting of aliphatic and aromatic divinyl compounds, diacrylates, dimethacrylates, diacrylamides, and dimethacrylamides.

30. A method of making polymeric toner particles according to claim 24, wherein said initiator is chosen from the group consisting of 2,2'"'"'-azobis(dimethyl valeronitrile), azobisisobutyronitrile, lauroyl peroxide, and azobismethylethylacetonitrile.

31. A method of making polymeric toner particles according to claim 24, wherein said stabilizer is chosen from the group consisting of silica, alumina, barium sulfate, calcium sulfate, barium carbonate, calcium carbonate, calcium phosphate, and latex-based copolymers.

32. A method of making polymeric toner particles according to claim 31, wherein said stabilizer is silica and further comprises the step of separating said silica stabilizer from the surface of said polymeric toner particles.

33. A method of making polymeric toner particles according to claim 24, wherein said promoters are chosen from the group consisting of poly(adipic acid-co-methylaminoethanol) and poly(diethanolamine adipate).

34. A method of making polymeric toner particles according to claim 24, wherein the droplets of the organic phase contain addenda chosen from the group consisting of colorants, and charge control agents.

35. A method of making polymeric toner particles according to claim 24, further comprising the step of mixing said polymeric toner particles with solid carrier particles to form a two component developer.

36. An electrographic toner composition comprising:

a particulate block copolymer having polyester blocks and polyvinyl blocks, wherein said polyester blocks and said polyvinyl blocks are linked together by a sulfide group and

addenda selected from the group consisiting of charge control agents and colorants.

37. An electrographic toner composition comprising:

a particulate block copolymer which is the polymerization product of a vinyl monomer and a chain transfer polyester, said chain transfer polyester containing a disulfide linkage and

addenda selected from the group consisting of charge control agents and colorants.

38. The toner composition according to claim 37, wherein said particulate block copolymer has an average particle size of 0.2-60 μ

m and a relatively narrow particle size distribution.