Encapsulated toner compositions and processes thereof

Claim 2

A toner composition comprised of a core comprised of pigments, dyes or mixtures thereof, and a polymer; and wherein the core is encapsulated in a telechelic polyester shell obtained by reacting a polyester with acid halide terminating groups thereon with a mono, di, or polyfunctional nucleophile, whereby the acid halide terminating groups of the polyester react with said nucleophile.

Claim 3

A toner in accordance with claim 1 wherein the polyester shell is derived from telechelic polyesters.

Claim 4

A toner in accordance with claim 1 wherein the core polymer is comprised of a styrene acrylate, a styrene methacrylate, or a styrene butadiene.

Claim 5

A toner in accordance with claim 1 wherein the core polymer is derived from the polymerization of an acryloxy-, a methacryloxy-, or a styryl-functionalized polysiloxane and an acrylate, a methacrylate, a styryl, or other vinyl-functionalized monomer.

Claim 6

A toner in accordance with claim 1 wherein the pigment is carbon black, iron oxides, magnetites, or mixtures thereof.

Claim 7

A toner in accordance with claim 5 wherein the pigment selected is comprised of surface treated magnetite.

Claim 8

A toner in accordance with claim 1 wherein the pigment is cyan, yellow, magenta, red, green, blue, brown, or mixtures thereof.

Claim 9

A toner in accordance with claim 7 wherein the pigment or dye is selected from the group consisting of Heliogen Blue, Pylam Oil Blue, Pylam Oil Yellow, Pigment Blue, Pigment Violet, Pigment Red, Lemon Chrome Yellow, Toluidine Red, Bon Red, NOVAperm Yellow FGL, Hostaperm Pink E, Cinquasia Magenta, Oil Red, 2,9-dimethyl-substituted quinacridone, Dispersed Red, diazo dye, Solvent Red, copper tetra-4-(octadecyl sulfonamido) phthalocyanine, X-copper phthalocyanine, Anthrathrene Blue, diarylide yellow 3,3-dichlorobenzidene acetoacetanilides, Solvent Yellow, nitrophenyl amine sulfonamide, 2,5-dimethoxy-4-sulfonanilide phenylazo-4'-chloro-2,5-dimethoxy acetoacetanilide, and Permanent Yellow FGL.

Claim 10

A toner in accordance with claim 1 wherein the shell represents from about 5 to 30 percent by weight of the toner, the core binder polymer represents from about 20 to about 90 percent by weight of the toner, and the pigment represents from about 2 to about 75 percent by weight of toner.

Claim 11

A toner in accordance with claim 1 containing surface additives comprised of metal salts, metal salts of fatty acids, or colloidal silicas.

Claim 12

A toner in accordance with claim 10 wherein zinc stearate is selected.

Claim 13

A toner in accordance with claim 11 wherein the additives are present in an amount of from about 0.1 to about 5.0 weight percent.

Claim 14

A toner in accordance with claim 1 wherein the toner shell is prepared by interfacial polymerization.

Claim 15

A toner in accordance with claim 1 wherein the shell surface is coated with conductive components.

Claim 16

A toner in accordance with claim 14 wherein the conductive components are comprised of carbon blacks, graphite, or mixtures thereof.

Claim 17

A toner in accordance with claim 1 wherein the core monomers for the formation of the core polymer is selected from the group consisting of n-butyl acrylate, s-butyl acrylate, isobutyl acrylate, n-butyl methacrylate, s-butyl methacrylate, isobutyl methacrylate, benzyl acrylate, benzyl methacrylate, propyl acrylate, isopropyl acrylate, hexyl acrylate, cyclohexyl acrylate, hexyl methacrylate, cyclohexyl methacrylate, lauryl acrylate, lauryl methacrylate, pentyl acrylate, pentyl methacrylate, stearyl acrylate, stearyl methacrylate, ethoxypropyl acrylate, ethoxypropyl methacrylate, heptyl acrylate, heptyl methacrylate, methylbutyl acrylate, methylbutyl methacrylate, m-tolyl acrylate, dodecyl styrene, hexylmethyl styrene, nonyl styrene, and tetradecyl styrene.

Claim 18

A toner composition in accordance with claim 1 wherein the diacid halide is a diacid chloride.

Claim 19

A toner composition in accordance with claim 1 wherein there results a linear, block, or branched polyester.

Claim 20

A process for the preparation of encapsulated toners which comprises preparing a mixture containing at least one core monomer, pigment, dye or mixtures thereof, radical initiators and a diacid halide monomer; dispersing the mixture into a emulsifier solution; adding to the resulting oil-in-water suspension a solution of bisphenolate and a catalyst thereby forming an acid halide terminated shell prepolymer through interfacial polymerization; subsequently adding to the suspension nucleophilic monomers capable of reacting with the terminal acid halide groups to form a polyester shell with functional groups thereon, which shell encapsulates the core components.

Claim 21

A process for the preparation of encapsulated toners which comprises preparing a mixture containing at least one core monomer, pigment, dye or mixtures thereof, radical initiators and a diacid halide monomer; dispersing the mixture into a emulsifier solution; adding to the resulting oil-in-water suspension a solution of bisphenolate and a catalyst thereby forming an acid halide terminated shell prepolymer through interfacial polymerization; subsequently adding to the suspension nucleophilic monomers capable of reacting with the terminal acid halide groups to form a polyester shell with functional groups thereon, which shell encapsulates the core components.

Claim 22

A process for the preparation of encapsulated toner compositions comprised of a core component and a shell component derived from a reactive polyester, which process comprises (1) providing a pigment dispersion comprised of at least one monomer capable of being polymerized by free radical polymerization, pigment, dye or mixtures thereof, and a free radical initiator, a polymer and an oil soluble shell monomer or monomers; (2) dispersing the aforementioned dispersion in an aqueous phase containing an emulsifier, an optional surfactant, an optional antifoaming agent, and an optional phase transfer catalyst; (3) adding less than a stoichiometric amount of a water soluble shell monomer to initiate the first stage of interfacial polymerization thereof; (4) adding a neucleophile to react with the aforementioned shell monomer thereof completing the formation of the shell; (5) heating the aqueous suspension of the encapsulated particles thereby effecting in situ polymerization of the core monomers; (6) washing the resulting toner product with deionized water; and (7) drying the washed toner product.

Claim 23

A process for the preparation of encapsulated toner compositions comprised of a core component and a shell component derived from a reactive polyester, which process comprises (1) providing a pigment dispersion comprised of at least one monomer capable of being polymerized by free radical polymerization, pigment, dye or mixtures thereof, and a free radical initiator, a polymer and an oil soluble shell monomer or monomers; (2) dispersing the aforementioned dispersion in an aqueous phase containing an emulsifier, an optional surfactant, an optional antifoaming agent, and an optional phase transfer catalyst; (3) adding less than a stoichiometric amount of a water soluble shell monomer to initiate the first stage of interfacial polymerization thereof; (4) adding a neucleophile to react with the aforementioned shell monomer thereof completing the formation of the shell; (5) heating the aqueous suspension of the encapsulated particles thereby effecting in situ polymerization of the core monomers; (6) washing the resulting toner product with deionized water; and (7) drying the washed toner product.

Claim 24

A process in accordance with claim 20 wherein the reactive polyester shell is derived from diacid halides.

Claim 25

A process in accordance with claim 21 wherein the diacid halides are comprised of diacid chlorides.

Claim 26

A process for the preparation of encapsulated toners which comprises preparing a pigment mixture containing core monomers, pigments, dyes or mixtures thereof, free radical initiators and diacid halide shell monomers; dispersing the mixture in an aqueous solution containing emulsifiers and a phase transfer catalyst; adding to the resulting suspension a bisphenolate solution, which was prepared by dissolving bisphenol in an aqueous sodium or potassium hydroxide solution, whereby the bisphenolate and diacid halide react to form an acid halide terminated reactive polyester, and subsequently adding to the solution nucleophilic monomers capable of reacting with the diacid halide terminated polyesters, thereby resulting in formation by interfacial polymerization of a modified polyester shell component surrounding the core components.

Claim 27

A process for the preparation of encapsulated toners which comprises preparing a pigment mixture containing core monomers, pigments, dyes or mixtures thereof, free radical initiators and diacid halide shell monomers; dispersing the mixture in an aqueous solution containing emulsifiers and a phase transfer catalyst; adding to the resulting suspension a bisphenolate solution, which was prepared by dissolving bisphenol in an aqueous sodium or potassium hydroxide solution, whereby the bisphenolate and diacid halide react to form an acid halide terminated reactive polyester, and subsequently adding to the solution nucleophilic monomers capable of reacting with the diacid halide terminated polyesters, thereby resulting in formation by interfacial polymerization of a modified polyester shell component surrounding the core components.

Claim 28

A process in accordance with claim 23 wherein the nucleophilic monomers are selected from the group consisting of amines, phenolates, thiophenolates, and mixtures thereof.

Claim 29

A process in accordance with claim 23 wherein the weight average molecular weight of the polyester shell is from about 5,000 to about 200,000.

Claim 30

A process for the preparation encapsulated toners which comprises (1) adding about 5 to 30 parts of a prepolymer and 10 to 30 parts of a predispersed magenta pigment powder into about 30 to 50 parts of a solution of vinyl core monomers; (2) mixing the aforementioned mixture with a mechanical shaker or a roll mill; (3) adding about 5 to 15 parts of an oil soluble first shell monomer or monomers and about 1 to 5 parts of free radical initiator or initiators to the mixture; (4) mixing the shell monomer(s) and the initiator(s) to provide a pigment dispersion comprised of the aforementioned components; (5) dispersing about 10 to 20 parts of the resulting dispersion into 50 to 200 parts of an aqueous emulsifier solution to provide an oil-in-water suspension; (6) adding to the suspension an aqueous solution of a second shell monomer or monomers at a molar ratio of about 0.9 to 1.0 with respect to the first shell monomer(s) to initiate interfacial polymerization and to form reactive polyester shells; (7) allowing the suspension to stir; (8) adding to the resulting suspension about 0.1 to 0.5 parts of a neucleophile; (9) adding to the resulting suspension from about 0.1 to 100 parts of an aqueous protective colloid solution; (10) heating the resulting suspension to accomplish free radical suspension polymerization of the core monomer or core monomers; (11) washing the resulting encapsulated toner particles; (12) sieving the washed toner particles and (14) thereafter drying the toner particles.

Claim 31

A process for the preparation encapsulated toners which comprises (1) adding about 5 to 30 parts of a prepolymer and 10 to 30 parts of a predispersed magenta pigment powder into about 30 to 50 parts of a solution of vinyl core monomers; (2) mixing the aforementioned mixture with a mechanical shaker or a roll mill; (3) adding about 5 to 15 parts of an oil soluble first shell monomer or monomers and about 1 to 5 parts of free radical initiator or initiators to the mixture; (4) mixing the shell monomer(s) and the initiator(s) to provide a pigment dispersion comprised of the aforementioned components; (5) dispersing about 10 to 20 parts of the resulting dispersion into 50 to 200 parts of an aqueous emulsifier solution to provide an oil-in-water suspension; (6) adding to the suspension an aqueous solution of a second shell monomer or monomers at a molar ratio of about 0.9 to 1.0 with respect to the first shell monomer(s) to initiate interfacial polymerization and to form reactive polyester shells; (7) allowing the suspension to stir; (8) adding to the resulting suspension about 0.1 to 0.5 parts of a neucleophile; (9) adding to the resulting suspension from about 0.1 to 100 parts of an aqueous protective colloid solution; (10) heating the resulting suspension to accomplish free radical suspension polymerization of the core monomer or core monomers; (11) washing the resulting encapsulated toner particles; (12) sieving the washed toner particles and (14) thereafter drying the toner particles.

Claim 32

An encapsulated toner composition comprised of the particles obtained by the process of claim 26, and pigment or dye particles.

Claim 33

A toner composition in accordance with claim 27 wherein the pigment particles are selected from the group consisting of carbon black, magnetites, cyan, magenta, yellow, red, blue, green, brown, and mixtures thereof.

Claim 34

A toner composition in accordance with claim 1 wherein at least one monomer is selected for the polymer core.

Claim 35

A toner composition in accordance with claim 1 wherein from 2 to about 20 monomers are selected.

Claim 36

A toner comprised of a core comprised of at least one polymer, and pigment, dye or mixtures thereof; and wherein the core is encapsulated in a polyester shell obtained from a diacid halide terminated polyester component obtained by reacting a polyester with acid halide terminating groups thereon with a mono, di, or polyfunctional nucleophile.

Claim 37

A toner comprised of a core comprised of at least one polymer, and pigment, dye or mixtures thereof; and wherein the core is encapsulated in a polyester shell obtained from a diacid halide terminated polyester component obtained by reacting a polyester with acid halide terminating groups thereon with a mono, di, or polyfunctional nucleophile.

Claim 38

A toner in accordance with claim 31 wherein from about 2 to about 10 polymers are present.

Claim 39

A toner composition comprised of a core comprised of pigments and a polymer, and wherein the core is encapsulated in a polyester shell obtained by reacting a polyester with acid halide terminating groups thereon with a mono, di, or polyfunctional nucleophile.

Claim 40

A toner composition comprised of a core comprised of pigments and a polymer, and wherein the core is encapsulated in a polyester shell obtained by reacting a polyester with acid halide terminating groups thereon with a mono, di, or polyfunctional nucleophile.

Claim 41

An encapsulated toner in accordance with claim 1 wherein the polyester is formed by the reaction of a bisphenol and a diacid halide to form an acid halide terminated reactive polyester, subsequently adding a nucleophilic monomer capable of reacting with a diacide halide terminated polyester thereby resulting in formation by interfacial polymerization of a modified polyester shell.

Claim 42

An encapsulated toner in accordance with claim 33 wherein the nucleophile is comprised of amino, phenolic or thiophenolic compounds.

Claim 43

An encapsulated toner composition comprised of a core comprised of pigment particles and a polymer; wherein the core is encapsulated in a telechelic polyester shell, which shell is obtained by the reaction of a diacid halide with a polyhydroxy compound thereby resulting in a polyester shell with diacid halide terminating groups thereon; subsequently reacting the resulting polyester with a mono, di, or polyfunctional nucleophile resulting in a final polyester shell whereby the acid halide groups of the polyester have been reacted with said nucleophile.

Claim 44

An encapsulated toner composition comprised of a core comprised of pigment particles and a polymer; wherein the core is encapsulated in a telechelic polyester shell, which shell is obtained by the reaction of a diacid halide with a polyhydroxy compound thereby resulting in a polyester shell with diacid halide terminating groups thereon; subsequently reacting the resulting polyester with a mono, di, or polyfunctional nucleophile resulting in a final polyester shell whereby the acid halide groups of the polyester have been reacted with said nucleophile.

Claim 45

An encapsulated toner in accordance with claim 36 wherein the nucleophile is selected from the group consisting of butylaniline, phenylaniline, chloroaniline, trifluoromethylaniline, butoxyaniline, aminobenzonitrile, bis(trifluoromethyl)aniline, aminophenyl, sodium or potassium aminoethane sulfonate, sodium aminonaphthalenesulfonate or potassium aminonaphthalenesulfonate, sodium aminobenzoate or potassium aminobenzoate, and butyl thiophenol.

Claim 46

An encapsulated toner in accordance with claim 1 wherein the nucleophile is selected from the group consisting of butylaniline, phenylaniline, chloroaniline, trifluoromethylaniline, butoxyaniline, aminobenzonitrile, bis(trifluoromethyl)aniline, aminophenyl, sodium or potassium aminoethane sulfonate, sodium or potassium aminonaphthalenesulfonate, sodium or potassium aminobenzoate, and butyl thiophenol.