Toner, developer using the toner, image forming apparatus
US-9519235-B2 · Dec 13, 2016 · US
US9176406B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9176406-B2 |
| Application number | US-201313958745-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 5, 2013 |
| Priority date | Aug 17, 2012 |
| Publication date | Nov 3, 2015 |
| Grant date | Nov 3, 2015 |
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Toner contains a binder resin containing a crystalline resin having a urethane and/or urea bonding; and a colorant, wherein in a diffraction spectrum of the toner as measured by an X-ray diffraction instrument, a ratio {C/(C+A)} of an integral intensity C of the spectrum derived from the crystalline structure to an integral intensity A of the spectrum derived from the non-crystalline structure is 0.12 or greater, wherein the toner satisfies the following relation 1: T1−T2≦30° C. (Relation 1), where T1 represents the maximum endothermic peak in the first temperature rising from 0° C. to 100° C. at the temperature rising rate of 10° C./min and T2 represents the maximum exothermic peak in the first temperature falling from 100° C. to 0° C. at the temperature falling rate of 10° C./min as T1 and T2 are measured by diffraction scanning calorimetry (DSC).
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What is claimed is: 1. A toner, comprising: a binder resin comprising a crystalline polyester resin having a urethane and/or urea bonding; and a colorant, wherein in a diffraction spectrum of the toner as measured by an X-ray diffraction instrument, a ratio {C/(C+A)} of an integral intensity C of a spectrum derived from a crystalline structure to an integral intensity A of a spectrum derived from a non-crystalline structure is 0.16 or greater, wherein the toner satisfies the following relation 1: T 1− T 2≦30° C. Relation 1 where T1 represents a maximum endothermic peak in a first temperature rising from 0° C. to 100° C. at a temperature rising rate of 10° C./min and T2 represents a maximum exothermic peak in a first temperature falling from 100° C. to 0° C. at a temperature falling rate of 10° C./min as T1 and T2 are measured by diffraction scanning calorimetry (DSC). 2. The toner according to claim 1 , wherein T2 satisfies the following relation 2: T 2≧30° C. Relation 2 3. The toner according to claim 1 , wherein the crystalline polyester resin further comprises a non-modified crystalline resin. 4. The toner according to claim 3 , wherein a ratio of the non-modified crystalline polyester resin is from 2% by weight to less than 50% by weight in the crystalline resin. 5. The toner according to claim 1 , further comprising a nucleating agent. 6. The toner according to claim 1 , wherein a melt molded product of the toner has a Martens hardness of 20 N/m 2 or more at 50° C. 7. The toner according to claim 1 , wherein a tetrahydrofuran soluble of the toner contains a component having a molecular weight of 100,000 or greater in an amount of 5.0% or greater of a peak area in a molecular weight distribution as measured by gel permeation chromatography, wherein a ratio of decomposed residue of the tetrahydrofuran soluble insoluble in methanol is 5.0% by weight or greater when the tetrahydrofuran soluble is decomposed in 0.1 N KOH methanol solution. 8. The toner according to claim 1 , wherein the crystalline polyester resin having a urethane and/or urea bonding comprises a crystalline polyester polyester resin having a urea bonding. 9. The toner according to claim 1 , wherein the crystalline polyester resin having a urethane and/or urea bonding comprises a crystalline polyester resin having a urethane and/or urea bonding formed by elongating a modified crystalline polyester resin having an isocyanate group at an end thereof. 10. The toner according to claim 1 , wherein TI satisfies the following relation 3: 50° C.< T 1<70° C. Relation 3. 11. The toner according to claim 1 , prepared by granulating toner particles by dispersing and/or emulsifying in an aqueous medium an oil phase in which a toner composition comprising a binder resin, a coloring agent, and an organically modified laminate inorganic mineral is dissolved and/or dispersed in an organic solvent. 12. The toner according to claim 11 , wherein elongation reaction is conducted between an active hydrogen group and a modified crystalline polyester resin having an isocyanate group at an end thereof when granulating the toner particles by dispersion and/or emulsification in the aqueous medium. 13. A development agent comprising: the toner of claim 1 ; and carrier. 14. The toner according to claim 1 , which further comprises a releasing agent. 15. The toner according to claim 14 , wherein the releasing agent accounts for 3 parts by weight to 10 parts by weight to 100 parts by weight of the toner. 16. The toner according to claim 1 , wherein the content of the crystalline polyester resin in the toner is 75% by weight or more. 17. The toner according to claim 1 , wherein the content of the crystalline polyester resin in the toner is 80% by weight or more. 18. A process cartridge comprising: a latent electrostatic image bearing member to bear a latent electrostatic image; and a development device to develop the latent electrostatic image with a toner to form a visible image, wherein the development device contains the toner of claim 1 , wherein the process cartridge is detachably attachable to an image forming apparatus.
Polyureas; Polyurethanes · CPC title
Polyesters · CPC title
characterised by their chemical properties, e.g. acidity, molecular weight, sensitivity to reactants · CPC title
characterised by their physical properties, e.g. viscosity, solubility, melting temperature, softening temperature, glass transition temperature · CPC title
whereby the components are brought together in a liquid dispersing medium · CPC title
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