Pigments for electrophoretic displays

US11248122B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11248122-B2
Application numberUS-201816234363-A
CountryUS
Kind codeB2
Filing dateDec 27, 2018
Priority dateDec 30, 2017
Publication dateFeb 15, 2022
Grant dateFeb 15, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A polysiloxane-substituted quinacridone pigment is produced by a quinacridone pigment with an epoxy-terminated polysiloxane under conditions effective to cause the epoxy group on the polysiloxane to react with, and bond the polysiloxane to, the quinacridone pigment. The quinacridone pigment thus produced has the polysiloxane grouping bonded to one of the quinacridone nitrogen atoms via a hydrocarbon linking group, which bears a hydroxyl group on a carbon atom α or β to the quinacridone nitrogen atom. These quinacridone pigments are useful in electrophoretic displays.

First claim

Opening claim text (preview).

The invention claimed is: 1. A quinacridone pigment comprising a polysiloxane-substituted quinacridone, in which a polysiloxane grouping is bonded to one of the quinacridone nitrogen atoms via a hydrocarbon linking group or a 3-alkoxypropyl linking group, the linking group bearing a hydroxyl group on a carbon atom β to the quinacridone nitrogen atom, the polysiloxane-substituted quinacridone being prepared by the reaction between quinacridone pigment particles and an epoxy-terminated polysiloxane in an organic solvent. 2. The quinacridone pigment of claim 1 , wherein the polysiloxane-substituted quinacridone is of the formula: where each R independently is a hydrogen, C 1 -C 3 alkyl group, or a halogen, L is a hydrocarbon linking group or a 3-alkoxypropyl linking group, Sil is a polysiloxane grouping, and the broken line indicated that the hydroxyl substituent is attached to a carbon atom β to the quinacridone nitrogen atom. 3. The quinacridone pigment of claim 2 wherein Sil represents the residue of a polydialkylsiloxane. 4. The quinacridone pigment of claim 2 wherein both R groups are methyl groups. 5. An electrophoretic medium comprising particles of a pigment according to claim 1 dispersed in a fluid. 6. The electrophoretic medium of claim 5 further comprising at least two types of pigment particles other than the quinacridone pigment particles of claim 2 , the three types of pigment particles having colors differing from each other. 7. The electrophoretic medium of claim 5 further comprising, in addition to the fluid: (a) a plurality of first and a plurality of second particles dispersed in the fluid the first and second particles bearing charges of opposite polarity, the first particle being a light-scattering particle and the second particle having one of the subtractive primary colors; and (b) a plurality of third and a plurality of fourth particles dispersed in the fluid, the third and fourth particles bearing charges of opposite polarity, the third and fourth particles each having a subtractive primary color different from each other and from the second particles, wherein the electric field required to separate an aggregate formed by the third and the fourth types of particles is greater than that required to separate an aggregate formed from any other two types of particles. 8. The electrophoretic medium of claim 5 further comprising, in addition to the fluid: (a) a plurality of first and a plurality of fourth particles dispersed in the fluid the first and fourth particles bearing charges of opposite polarity and each having a polymer coating comprising at least about 60 percent by weight of an acrylate or methacrylate ester monomer wherein the ester group comprises a hydrocarbon chain comprising at least about six carbon atoms, one of the first and fourth particles being a light-scattering particle and the other of the first and fourth particles being a substantially non-light-scattering particle having one of the subtractive primary colors; (b) a plurality of second particles dispersed in the fluid, the second particles bearing charges of the same polarity as the fourth particles, having a polymer coating comprising at least about 60 percent by weight of a polydimethylsiloxane-containing monomer, and having a subtractive primary color different from the substantially non-light-scattering one of the first and fourth particles, the second particles being pigment particles of the present invention; and (c) a plurality of third particles bearing charges of the same polarity as the first particles, being substantially non-light scattering and having a subtractive primary color different from the substantially non-light-scattering one of the first and fourth particles and different from that of the second particles. 9. An electrophoretic display comprising a layer of an electrophoretic medium according to claim 5 and at least one electrode disposed adjacent the layer of electrophoretic medium and arranged to apply an electric field thereto.

Assignees

Inventors

Classifications

  • Polymers attached to the pigment surface (C09B68/444, C09B68/446 take precedence) · CPC title

  • condensed with carbocyclic rings · CPC title

  • by electrophoresis · CPC title

  • of organic pigments with only macromolecular substances · CPC title

  • Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds · CPC title

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Frequently asked questions

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What does patent US11248122B2 cover?
A polysiloxane-substituted quinacridone pigment is produced by a quinacridone pigment with an epoxy-terminated polysiloxane under conditions effective to cause the epoxy group on the polysiloxane to react with, and bond the polysiloxane to, the quinacridone pigment. The quinacridone pigment thus produced has the polysiloxane grouping bonded to one of the quinacridone nitrogen atoms via a hydroc…
Who is the assignee on this patent?
E Ink Corp
What technology area does this patent fall under?
Primary CPC classification C09B47/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 15 2022 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 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).