Toner, image forming apparatus, image forming method, and toner stored unit

US10310399B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10310399-B2
Application numberUS-201515536531-A
CountryUS
Kind codeB2
Filing dateNov 26, 2015
Priority dateDec 19, 2014
Publication dateJun 4, 2019
Grant dateJun 4, 2019

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  5. First independent claim

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Abstract

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Provided is a toner including at least a binder resin, and having peak ratio W/R of from 0.20 to 0.70 when measured with FT-IR according to ATR method, W/R being a ratio of height W of maximum spectral peak attributed to bisphenol A skeleton of the toner and observed at from 1,480 cm−1 to 1,520 cm−1 to height R of maximum spectral peak attributed to carbonyl group of the toner and observed at from 1,700 cm−1 to 1,750 cm−1, wherein molecular weight distribution of the toner obtained by GPC of THF-soluble component of the toner has main peak in a range of from 1,000 to 10,000, half value width of the molecular weight distribution is a molecular weight of 20,000 or less, and content of a THF-insoluble component in the toner is from 5% by mass to 40% by mass.

First claim

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The invention claimed is: 1. A toner, comprising a binder resin comprising a polyester resin, wherein an alcohol component constituting the polyester resin comprises a bisphenol A component, wherein the toner has a peak ratio W/R of from 0.20 to 0.70 when measured according to a Fourier Transform InfraRed spectroscopic analysis (FT-IR) method according to an Attenuated Total Reflection (ATR) method, where the peak ratio W/R is a ratio of a height W of a maximum spectral peak attributed to a bisphenol A skeleton of the toner and observed at from 1,480 cm −1 to 1,520 cm −1 to a height R of a maximum spectral peak attributed to a carbonyl group of the toner and observed at from 1,700 cm −1 to 1,750 cm −1 , wherein a molecular weight distribution of the toner obtained by Gel Permeation Chromatography (GPC) of a tetrahydrofuran (THF)-soluble component of the toner has a main peak in a range of from 1,000 to 10,000, and a half value width of the molecular weight distribution is a molecular weight of 20,000 or less, and wherein a content of a THF-insoluble component in the toner is from 5% by mass to 40% by mass. 2. The toner according to claim 1 , wherein the toner has a peak ratio W′/R′ of from 0.06 to 0.70 when measured according to a Fourier Transform InfraRed spectroscopic analysis (FT-IR) method according to infrared spectroscopy (KBr tablet method), where the peak ratio W′/R′ is a ratio of a height W′ of a spectral peak of the toner observed at from 1,480 cm −1 to 1,520 cm −1 to a height R′ of a spectral peak of the toner observed at from 1,700 cm −1 to 1,750 cm −1 . 3. The toner according to claim 2 , wherein the peak ratio W/R and the peak ratio W′/R′ satisfies a relationship below, W′/R′≤W/R. 4. The toner according to claim 2 , wherein a ratio (W/R)/(W′/R′) of the peak ratio W/R to the peak ratio W′/R′ is from 1.0 to 2.0. 5. The toner according to claim 1 , wherein a content of the bisphenol A component in a THF-soluble alcohol component of the toner is from 20 mol % to 100 mol %, wherein a content of the bisphenol A component in a THF-insoluble alcohol component of the toner is from 0 mol % to 80 mol %, and wherein the content of the bisphenol A in the THF-soluble alcohol component is greater than the content of the bisphenol A in the THF-insoluble alcohol component. 6. The toner according to claim 1 , wherein the content of the THF-insoluble component in the toner is from 10% by mass to 35% by mass. 7. An image forming method, comprising: forming an electrostatic latent image over an electrostatic latent image bearer; developing the electrostatic latent image formed over the electrostatic latent image bearer with a toner according to claim 1 to form a toner image, transferring the toner image formed over the electrostatic latent image bearer onto a recording medium; and fixing the toner image transferred onto the recording medium. 8. A toner stored unit, comprising a toner, wherein the toner stored unit stores the toner, wherein the toner comprises a binder resin comprising a polyester resin, wherein an alcohol component constituting the polyester resin comprises a bisphenol A component, wherein the toner has a peak ratio W/R of from 0.20 to 0.70 when measured according to a Fourier Transform InfraRed spectroscopic analysis (FT-IR) method according to an Attenuated Total Reflection (ATR) method, where the peak ratio W/R is a ratio of a height W of a maximum spectral peak attributed to a bisphenol A skeleton of the toner and observed at from 1,480 cm −1 to 1,520 cm −1 to a height R of a maximum spectral peak attributed to a carbonyl group of the toner and observed at from 1,700 cm −1 to 1,750 cm −1 , wherein a molecular weight distribution of the toner obtained by Gel Permeation Chromatography (GPC) of a tetrahydrofuran (THF)-soluble component of the toner has a main peak in a range of from 1,000 to 10,000, and a half value width of the molecular weight distribution is a molecular weight of 20,000 or less, and wherein a content of a THF-insoluble component in the toner is from 5% by mass to 40% by mass. 9. An image forming apparatus, comprising: an electrostatic latent image bearer; a charging unit configured to electrically charge the electrostatic latent image bearer; an electrostatic latent image forming unit configured to form an electrostatic latent image over the electrically charged electrostatic latent image bearer; a developing unit configured to develop the electrostatic latent image formed over the electrostatic latent image bearer with a toner to form a toner image; a transfer unit configured to transfer the toner image formed over the electrostatic latent image bearer onto a recording medium; and a fixing unit configured to fix the toner image transferred onto the recording medium, wherein the toner comprises a binder resin comprising a polyester resin, wherein an alcohol component constituting the polyester resin comprises a bisphenol A component, wherein the toner has a peak ratio W/R of from 0.20 to 0.70 when measured according to a Fourier Transform InfraRed spectroscopic analysis (FT-IR) method according to an Attenuated Total Reflection (ATR) method, where the peak ratio W/R is a ratio of a height W of a maximum spectral peak attributed to a bisphenol A skeleton of the toner and observed at from 1,480 cm −1 to 1,520 cm −1 to a height R of a maximum spectral peak attributed to a carbonyl group of the toner and observed at from 1,700 cm −1 to 1,750 cm −1 , wherein a molecular weight distribution of the toner obtained by Gel Permeation Chromatography (GPC) of a tetrahydrofuran (THF)-soluble component of the toner has a main peak in a range of from 1,000 to 10,000, and a half value width of the molecular weight distribution is a molecular weight of 20,000 or less, and wherein a content of a THF-insoluble component in the toner is from 5% by mass to 40% by mass.

Assignees

Inventors

Classifications

  • G03G9/0821Primary

    characterised by physical parameters (magnetic parameters G03G9/083) · CPC title

  • by mixing the toner components in a liquefied state; melt kneading; reactive mixing · CPC title

  • Polyesters · CPC title

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

  • using a solid developer, e.g. powder developer · CPC title

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What does patent US10310399B2 cover?
Provided is a toner including at least a binder resin, and having peak ratio W/R of from 0.20 to 0.70 when measured with FT-IR according to ATR method, W/R being a ratio of height W of maximum spectral peak attributed to bisphenol A skeleton of the toner and observed at from 1,480 cm−1 to 1,520 cm−1 to height R of maximum spectral peak attributed to carbonyl group of the toner and observed at f…
Who is the assignee on this patent?
Matsushita Natsuko, Suzuki Tomomi, Ogino Kohtaroh, and 2 more
What technology area does this patent fall under?
Primary CPC classification G03G9/0821. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Jun 04 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).