WO2004090626A1 - 画像表示媒体に用いる粒子、それを用いた画像表示用パネル及び画像表示装置 - Google Patents
画像表示媒体に用いる粒子、それを用いた画像表示用パネル及び画像表示装置 Download PDFInfo
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- WO2004090626A1 WO2004090626A1 PCT/JP2004/004854 JP2004004854W WO2004090626A1 WO 2004090626 A1 WO2004090626 A1 WO 2004090626A1 JP 2004004854 W JP2004004854 W JP 2004004854W WO 2004090626 A1 WO2004090626 A1 WO 2004090626A1
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- display medium
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/165—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on translational movement of particles in a fluid under the influence of an applied field
- G02F1/166—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on translational movement of particles in a fluid under the influence of an applied field characterised by the electro-optical or magneto-optical effect
- G02F1/1671—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on translational movement of particles in a fluid under the influence of an applied field characterised by the electro-optical or magneto-optical effect involving dry toners
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/165—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on translational movement of particles in a fluid under the influence of an applied field
- G02F1/166—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on translational movement of particles in a fluid under the influence of an applied field characterised by the electro-optical or magneto-optical effect
- G02F1/167—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on translational movement of particles in a fluid under the influence of an applied field characterised by the electro-optical or magneto-optical effect by electrophoresis
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/165—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on translational movement of particles in a fluid under the influence of an applied field
- G02F1/1675—Constructional details
- G02F2001/1678—Constructional details characterised by the composition or particle type
Definitions
- the present invention relates to a particle and a powder fluid used in a reversible image display device capable of repeatedly displaying an image by utilizing movement of a particle or a powder fluid by electrostatic force such as Coulomb force, and an image using the same.
- the present invention relates to a display panel and an image display device.
- an image display device that replaces the liquid crystal (LCD)
- LCD liquid crystal
- an image display device display
- technologies such as an electrophoresis system, an electrochromic system, a thermal system, and a two-color particle rotating system
- These image display devices are considered as next-generation inexpensive display devices because of their advantages such as obtaining a wide viewing angle close to ordinary printed matter, low power consumption, and having a memory function as compared with LCDs. It is expected to be applied to display for mobile terminals and electronic paper.
- a dry image display device including an image display plate having one or more image display elements is known.
- an image display element is formed by disposing a partition between a transparent substrate and a counter substrate.
- the dry-type image display device described above has the advantage that the particle movement resistance is smaller and the response speed is faster! / Compared to the electrophoresis method.
- the principle of image display in this dry-type image display device is that a pattern is formed by each particle and the pattern is recognized by obtaining a contrast by the color tone of each particle. For this reason, the luminance factor of the white particles, which are to reflect light, was important.
- white particles are produced by mixing fine particles of a material with a high refractive index into a material with a low refractive index. Had limitations.
- the behavior of particles in a substrate provided with actual electrodes is such that all particles of the same polarity do not adhere uniformly to one electrode, but rather In some cases, the same particles often form agglomerates within the substrate. In such a case, there is a problem that the display characteristics are remarkably deteriorated due to a decrease in particles attached to the display electrode surface.
- the dry-type image display device described above has an advantage that the moving resistance of particles is smaller and the response speed is faster than the electrophoretic method.
- the principle of image display in this dry-type image display device is that a pattern is formed by each particle and the pattern is recognized by obtaining a contrast by the color tone of each particle. Therefore, the color of the white particles, which are the bases for emitting the color, was important.
- colored particles such as white particles
- pigments and dyes are kneaded into a polymer
- pulverized particles obtained by pulverization and classification and pigments obtained by various polymerization methods such as suspension polymerization, emulsion polymerization, seed polymerization, etc.
- Polymer particles obtained by enclosing a dye, composite particles having pigments, dyes, and the like adhered to the surface of mother particles, and the like are known.
- the pulverized particles have a problem in that the particle shape varies, the filling amount of pigments and dyes is limited, a predetermined color cannot be obtained, and damage such as cracks is generated at the time of pulverization.
- the polymer particles have a problem that the filling amount of the pigment or the dye is further smaller and a predetermined color cannot be obtained.
- composite grains In the case of pigments, there were problems in that coloring was insufficient due to the absence of pigments and dyes inside the base particles, that the pigments and dyes were easily peeled off from the surface, and that the number of production steps was increased.
- the dry-type image display device described above has an advantage that the moving resistance of particles is smaller and the response speed is faster than the electrophoretic method.
- the principle of image display in this dry-type image display device is that a pattern is formed by each particle and the pattern is recognized by obtaining a contrast by the color tone of each particle. Therefore, the color of the white particles, which are the bases for emitting the color, was important.
- such white particles are titanium oxide (T i 0 2), zinc oxide, a white pigment such as oxidation Jill Koniumu, are prepared by filling a resin as a base.
- a polymerization method and a kneading and pulverizing method as the production method, and the kneading and pulverizing method can add a large amount of pigment such as titanium oxide and is excellent in whiteness.
- a spherical body can be obtained by the polymerization method, but it becomes indeterminate by the kneading and pulverizing method.
- the amount of the white pigment to be filled is up to 50 parts by weight in the polymerization method with respect to 100 parts by weight of the base resin, but can be filled up to about 300 parts by weight in the kneading and pulverizing method.
- the polymerization method and the kneading and pulverizing method each have advantages and disadvantages, but the kneading and pulverizing method is often used in terms of the most important whiteness.
- the maximum whiteness is about 200 parts by weight of titanium oxide with respect to 100 parts by weight of the base resin. If the amount of titanium oxide exceeds 300 parts by weight, kneading becomes difficult, and the white reflectance decreases. In particular, with titanium oxide or the like, there was a problem that it was difficult to fill 300 parts by weight or more with respect to 100 parts by weight of the base resin.
- particles used in an image display device having such a dry image display panel conventionally, a pigment, a charge control agent, and the like are melted, kneaded, and then ground using a thermoplastic resin such as polycarbonate (PC) as a base resin.
- a thermoplastic resin such as polycarbonate (PC)
- particles obtained by the above method are used.
- Particles obtained by the kneading-pulverization method using a thermoplastic resin as a base resin in this manner have low heat resistance, and are used under high-temperature conditions such as the use environment of image display panels at high temperatures and the bonding process of image display panels. During the operation, there was a problem that the particles melted and adhered and aggregated on the image display panel.
- An object of the first invention of the present invention is to solve the above-mentioned problems, and to reduce an amount of light transmitted through even a thin image display medium layer, to increase backscattering and to improve a white luminance factor. It is an object of the present invention to provide white particles to be used and an image display device using the same.
- the white particles according to the first invention of the present invention are: an image display device that encloses an image display medium between opposed substrates at least one of which is transparent, applies an electric field to the image display medium, moves the image display medium, and displays an image.
- a central portion and an outer layer portion covering the central portion, wherein the central portion has a total reflectance of 70% or more at the interface between the central portion and the outer layer portion, and the outer layer portion has at least It is characterized by comprising a resin layer in which fine particles of a high refractive index material are mixed with one or more low refractive index materials.
- the white particles of the present invention can improve the white luminance factor by having a central part exhibiting high total reflectance.
- the white particles according to the first invention of the present invention include: a central portion being solid or hollow metal particles; a central portion being particles in which a resin layer is coated with a metal film;
- the interface between the part and the outer layer part is a reflective film composed of a multilayer film, the diameter of the central part is 50 to 95% of the particle diameter, and the average particle diameter d (0.5) is 0. 1 to 5 O xm, the resin layer as the outer layer, the surface of which is treated with a coupling agent, and the resin layer, as the outer layer, has a strong charge on the surface.
- Coated with a transparent resin Coated with a transparent resin.
- the luminance factor of the white particles can be further improved by embodying the configuration.
- the image display device according to the first invention of the present invention, wherein an image display medium is sealed between opposing substrates, at least one of which is transparent, applies an electric field to the image display medium, moves the image display medium, and displays an image.
- the image display device is characterized in that the white particles having the above-described configuration are used as at least one kind of image display medium.
- An object of the second invention of the present invention is to solve the above-mentioned problems and to provide an inexpensive image display panel and an image display device which are excellent in durability even in repeated use.
- An image display panel includes an image display medium having at least two or more different colors and different charging characteristics between opposing substrates, at least one of which is transparent, and applying an electric field to the image display medium.
- an image display panel for displaying an image by moving the image display medium here, at least two or more types of image display media having different colors and different charging characteristics are used. It is characterized by comprising at least three types of particles including substantially spherical particles and third particles having a particle size smaller than the two types of substantially spherical particles.
- a particle group consisting of three types of particles obtained by adding a third particle to two types of substantially spherical particles having different charging characteristics is sealed between two substrates.
- the two types of substantially spherical particles are both spherical and have a macroscopically smooth surface. If the surface is not macroscopically smooth or spherical, the rolling action of the third particles is less likely to be exhibited and the lubricating effect is less likely to be exerted, so that particle aggregation is likely to occur. Further, the third particles are also preferably spherical. By making the third particles spherical, the rolling action between the other two particles is enhanced, and the first and second particles are more likely to move (the lubrication effect between the two particles is increased), preventing aggregation of both particles. Effect is increased.
- Another preferred embodiment is that two kinds of substantially spherical particles having different colors and charging characteristics have an average particle diameter in the range of 0.5 to 50 ⁇ m and have substantially the same average particle diameter.
- the average particle diameter of the third particles is 20 to 200 nm, and the volume occupancy of at least two or more image display media filled between the substrates is 5 to 70 V o 1 May be in the% range.
- the present invention can be more suitably implemented.
- an image display device is characterized by including the above-described image display panel.
- An object of the third invention of the present invention is to solve the above-mentioned problems and to provide an image display medium and an image display device using the same, which can reduce generation of agglomerates due to particles of the same polarity. .
- An image display medium includes an image display medium comprising at least two types of colored particles having a charge property between two substrates that are opposed to each other and at least one of which is transparent; or An image used in an image display device that encloses an image display medium composed of one type of colored particles having a chargeability, applies an electric field to the particles from two types of electrodes having different potentials, moves the particles, and displays an image.
- an image display device of the present invention is characterized by utilizing the above-described image display medium.
- Preferable examples of the image display medium according to the third invention of the present invention include a particle having a relative dielectric constant ⁇ r of ⁇ r ⁇ 5.0, more preferably ⁇ r ⁇ 3.0, and a high dielectric constant inside the particles.
- the surface charge density is in the range of 5 to 150 ⁇ C / m 2 in absolute value. In any case, the present invention can be more suitably implemented.
- the relative permittivity Er of the particles is preferably ⁇ r ⁇ 5.0. If the relative dielectric constant ff exceeds 5.0, it is not possible to sufficiently prevent the generation of aggregates, as is apparent from the examples described later.
- an image display medium composed of particles made of a low dielectric insulating material having a relative dielectric constant ⁇ r of ⁇ r ⁇ 5.0.
- An object of the fourth invention of the present invention is to solve the above-mentioned problems, to provide white particles capable of greatly improving opacity (reflectance), an image display medium using the same, and an image display using the same. It is intended to provide a device.
- the white particles according to the fourth invention of the present invention are: an image display device that encapsulates an image display medium between opposed substrates, at least one of which is transparent, applies an electric field to the image display medium, moves the image display medium, and displays an image.
- White particles to be used for a binder comprising 27 particles having a predetermined particle size obtained by aggregating or granulating primary particles of a white pigment coated with a binder, and including microbubbles therein. It is.
- the white pigment having a surface coated with a binder preferably a titanium oxide pigment
- a binder preferably a titanium oxide pigment
- the hiding power of titanium oxide does not increase in proportion to the filling amount.
- the light scattering efficiency of the pigment decreases as the filling amount increases. At the rate, the obscurity shows a peak.
- the filling amount is further increased, it approaches the close-packed state, and fine bubbles are introduced, so that the concealing effect is improved at once.
- the present invention utilizes this phenomenon.
- the white particles according to the fourth invention of the present invention include that the white pigment is titanium oxide, that the binder is made of a low refractive index material, that the secondary particles are aggregated or granulated. Is mixed and stirred in a flowing air stream or mechanically to induce numerous fine bubbles.
- the image display device of the present invention is an image display device in which an image display medium is sealed between opposed substrates at least one of which is transparent, and an image is displayed by moving the image display medium by applying an electric field to the image display medium. Further, the above-mentioned white particles are used as at least one kind of image display medium.
- An object of the fifth invention of the present invention is to solve the above-mentioned problems and to provide an inexpensive image display panel and an image display device which are excellent in durability even in repeated use.
- the image display panel according to the first embodiment of the fifth invention of the present invention comprises at least two kinds of image display media sealed between opposed transparent substrates, at least one of which is composed of two types of electrodes having different potentials.
- One of the particles is a particle having macroscopic unevenness on the surface, and the other is a particle having no macroscopic unevenness on the surface.
- one of the particles used for two types of image display media having different charging characteristics is a particle having macroscopic irregularities on its surface (for example, powder).
- the surface characteristics of the particles used in two types of image display media are different, as the substantially spherical particles (e.g., polymer particles) without macroscopic irregularities on the surface. Particles are less likely to aggregate and adhere to each other, improving the durability of image display.
- Particles with the same charging characteristics exert repulsive forces on each other, so they are unlikely to aggregate even if they have the same macroscopic surface shape, but they attract each other Even if the particles exert different forces and have different charging characteristics, a macroscopically different surface shape can make the particles less likely to aggregate.
- One of the particles used for the image display medium of the above was a particle having macroscopic unevenness on the surface, and the other was a particle having no macroscopic unevenness on the surface and having fine particles electrostatically attached to the surface. It is a characteristic.
- one of the particles constituting the two types of image display media having different charging characteristics is a particle having macroscopic irregularities on its surface (for example, crushed particles)
- the other is a substantially spherical particle (for example, a polymer particle) having no macroscopic unevenness on the surface, and a fine particle having a charged polarity different from that of the particle having no macroscopic unevenness on the surface of the substantially spherical particle having no macroscopic unevenness.
- particles having the same charging characteristics exert a repulsive force on each other, but tend to adhere when there is no macroscopic unevenness on the surface, but there is no such macroscopic unevenness on the surface Aggregation can be reliably prevented by electrostatically attaching the fine particles to the surfaces of the particles having the same charging characteristics.
- the two types of particles having different charging characteristics can be made hard to aggregate by forming macroscopically different surface shapes (particles having macroscopic irregularities on the surface and particles having no macroscopic irregularities on the surface).
- Particles with macroscopic irregularities are obtained by crushing a tree Of the two types of image display media that have different charging characteristics and optical reflectivity, the particles with macroscopic irregularities on the surface are obtained by firmly attaching the fine particles to the surface of the base particles. Used to strongly adhere the base particles and the fine particles, and to use a mechanical impactor.
- the particles having no macroscopic convexity on the surface are substantially spherical particles obtained by polymerizing a resin monomer, and the particles constituting two types of image display media having different charging characteristics and optical reflectivity.
- particles having no macroscopic irregularities on the surface are substantially spherical particles obtained by exposing the pulverized particles to a temperature higher than the melting point of the particles to smooth the surface, and at least two particles to be filled between the substrates.
- the volume occupancy of the image display medium is in the range of 5 to 70 V o 1%, and the average particle diameter of the particles constituting the two types of image display media having different charging characteristics and optical reflectivity is 0.5 ⁇ 50 / im.
- the first and second embodiments according to the fifth invention of the present invention can be more suitably implemented.
- the second embodiment of the fifth invention of the present invention among particles constituting two types of image display media having different charging characteristics and optical reflectances, particles having no macroscopic unevenness on the surface.
- the fine particles to be electrostatically adhered to the surface have a polarity opposite to the charging polarity of the particles having no macroscopic irregularities on the surface, and after adhering to the surface, the particles having no macroscopic irregularities on the surface are charged.
- the polarity may not be changed, and the average particle diameter of the fine particles electrostatically attached to the particle surface having no macroscopic irregularities on the surface may be 20 to 200 nm.
- the second embodiment according to the fifth invention of the present invention can be more suitably implemented.
- an image display device is characterized in that the image display panel having the above-described configuration is mounted.
- An object of the sixth invention of the present invention is to solve the above-mentioned problems, and to provide a white face such as titanium oxide To provide white particles capable of improving the whiteness (white reflectance) without increasing the filling amount of the filler, a white powder fluid using the same, and an image display device using the same as an image display medium Things.
- the white particles according to the sixth invention of the present invention are: an image display device for enclosing an image display medium between opposed substrates at least one of which is transparent, applying an electric field to the image display medium, moving the image display medium, and displaying an image.
- the white particles used in the above are characterized in that a base resin is filled with white pigments and hollow particles.
- the whiteness (white reflectance) of the white particles is improved due to the hiding effect of the hollow particles. Can be done.
- the filling amount of the white pigment and the hollow particles with respect to the resin is 100 to 300 parts by weight of the white pigment with respect to 100 parts by weight of the resin.
- the particles may be from 10 to 60 parts by weight.
- the filling amount of the hollow particles is 100 to 60 parts by weight based on 100 parts by weight of the base resin.
- the amount is less than 10 parts by weight, the white reflectance is almost improved.
- no more than 60 parts by weight kneading with the resin becomes difficult.
- the white pigment is any of titanium oxide and zirconium oxide, and the composition of the hollow particles is cross-linked styrene-acryl.
- the average particle diameter d (0.5) is 1.0 to 5 O / xm. In any case, the whiteness of the white particles can be more effectively improved.
- the image display device of the present invention is an image display device in which an image display medium is sealed between opposed substrates at least one of which is transparent, and an image is displayed by moving the image display medium by applying an electric field to the image display medium.
- the above-mentioned white particles are used as at least one kind of image display medium.
- An object of the seventh invention of the present invention is to solve the above-mentioned problems and to provide an image display medium which has improved heat resistance and does not adhere to an image display panel and does not cause aggregation, and an image display apparatus using the same. It is something to try.
- An image display medium includes an image display medium enclosed between opposed substrates, at least one of which is transparent, an electric field applied to the image display medium, and the image display medium is moved to display an image.
- a thermosetting resin is used as a base resin of the particles constituting the image display medium, and after a resin material containing the thermosetting resin is kneaded and then subjected to a thermal crosslinking reaction after the kneading of the image display medium used in the image display device to be used. It is characterized by being obtained by grinding.
- heat resistance can be improved by using a thermosetting resin subjected to a thermal crosslinking reaction as a base resin of particles constituting the image display medium, As a result, adhesion and cohesion to the image display panel do not occur.
- the particles used in the image display medium according to the seventh aspect of the present invention include a thermosetting resin as a base, polyester resin + block isocyanate, alkyd resin + melamine curing agent, epoxy Resin + amine curing agent type, urea resin + formaldehyde type, and in addition to thermosetting resin as base resin, may include organotin catalyst, pigment, charge control agent .
- the present invention can be more suitably implemented.
- an image display device includes an image display panel using an image display medium using the above-described particles. Disclosure of the eighth invention>
- An object of an eighth invention of the present invention is to solve the above-mentioned problems, to provide an excellent image contrast, not to reduce the image contrast even when used repeatedly, and to provide a durable and inexpensive image display panel and image display device. It is intended to provide.
- An image display panel is the image display panel, wherein at least one of the opposite panels is transparent. At least two types of image display media are enclosed between two substrates, and an electric field is applied to the image display media to move the image display media to display an image.
- the present invention is characterized in that at least one of the two types of particles having different charging characteristics and optical reflectance contained in the image display medium has a flat round shape.
- At least one of the particles used for the two types of image display media having different charging characteristics and optical reflectivity is formed into a flat round particle, so that the particles move.
- the particles are arranged without gaps, and the gap between the particles is reduced, so that the image contrast is improved.
- the particles used for the two types of image display media having different charging characteristics and optical reflectivity are both flat round particles, it becomes difficult for the particles to aggregate and adhere to each other, and when the particles move. Collisions are reduced, and the durability of the image display is improved.
- the degree of flattening cannot be clearly specified, a sufficient effect can be obtained with a degree that is slightly flatter than a true spherical shape.
- the flat round particles are white particles
- the flat round white particles are titanium oxide
- the flat round-shaped atachiko is made by exposing a crushed piece made by crushing a resin sheet to a temperature higher than the melting point of the tree, and at least two types of images
- the average particle size of the particles used for the two types of image display media having different charging characteristics and optical reflectances contained in the display medium is 0.1 to 50 ⁇ m for each of the particles, and
- the volume occupancy of at least two or more types of image display media filled between the substrates may be in the range of 5 to 70 V o 1%. In any case, the present invention can be more suitably implemented.
- an image display device is characterized in that an image display panel using the image display medium having the above-described configuration is mounted.
- An object of a ninth invention of the present invention is to solve the above-mentioned problems, to provide an excellent image contrast, not to reduce the image contrast even when used repeatedly, and to provide a durable and inexpensive image display panel and image display device. It is intended to provide.
- An image display panel provides an image display medium including at least two types of particle groups having different colors and different charging characteristics between two opposed substrates at least one of which is transparent.
- an image display panel for enclosing, applying an electric field to the image display medium, and moving the image display medium to display an image two types of particle groups (color and charge characteristics different from each other) contained in the image display medium (The relationship between the particle diameters of the dark and dark color particles and the light and light color particles is Dbright ⁇ Dbright, where the average particle size of the light and light color particles is Dbright and the average of the dark and dark color particles is Ddark. It is characterized by being represented.
- the relationship between the particle diameters of the two kinds of particles having different colors and the charging characteristics is determined by the average particle diameter Ddark of the dark and dark particles and the average particle diameter of the light and light particles.
- Ddark ⁇ Dbright With the diameter Dbright, when the particles move in opposite directions according to the direction of the electric field between the substrates and are arranged on the display substrate surface, the relationship between the particle diameters is reversed.
- the contrast is improved. The reason for this is not clear, but the contrast improves when the light-colored particles are properly arranged on the display-side substrate surface. It is considered that they are arranged properly on the substrate surface and the contrast is improved.
- the effect is high in the reflection density of a white solid display image particularly when white particles are used as the light and bright color particles, and the particles constituting the dark and dark color particles are It is preferable that the particles constituting the light-colored particles are black and white.
- the degree of the relationship of Ddark and Dbright cannot be clearly defined, but a slight difference is sufficient, and a very large difference is rather bad. Therefore, it is preferable to set the range of 1 to DbrightZDdark and 2. Furthermore, the above relationship is satisfied for all particles constituting the particle group. Therefore, in the classification performed to equalize the particle diameters, it is preferable to perform an over power for the dark and dark particles and an under power for the light and light particles.
- At least two types of particle groups having different color and charge characteristics have a particle diameter in any particle group. 1 to 50 ⁇ , and the volume occupancy of the image display medium containing at least two kinds of particles having different colors and charge characteristics between the substrates is 5 to 70 ⁇ . V ⁇ ⁇ % range.
- the present invention can be implemented more effectively.
- an image display device is characterized in that an image display panel using the image display medium having the above-described configuration is mounted.
- An object of the tenth invention of the present invention is to solve the above-mentioned problems and provide a particle used for an image display medium capable of exhibiting charge control ability, a powder fluid using the same, and an image display device using the same. It is something to try.
- the first embodiment according to the tenth aspect of the particles used in the image display medium of the present invention is as follows.
- the image display medium is sealed between opposing substrates, at least one of which is transparent, and an electric field is applied to the image display medium.
- ⁇ metal element
- ⁇ oxygen
- X ⁇
- the image display medium is sealed between opposed substrates at least one of which is transparent, applying an electric field to the image display medium,
- M a metal element
- m, n, y, and z are integers, and are 4 ⁇ m ⁇ 22.
- the particles used for the image display medium according to the tenth aspect of the present invention include a metal element (M) having a positive ionization property of Pauling electronegativity of 0.79 ⁇ % ⁇ 1.91.
- the metal element may be one of Mg, Zn, Ca, Li, Zr, Al, Ni, Cu, Ba, and Ti.
- the poling electronegativity of the metal element (M) ion is 1.50 ⁇ % ⁇ 2.58 and the negative chargeability
- the metal element may be any one of Fe, Ti, Cu, Si, Sb, W, Sn, Ge, and Co. In any case, the present invention can be more suitably implemented.
- FIGS. 1A and 1B are diagrams each showing an example of a display method in an image display device to which the present invention is applied.
- 2 (a) and 2 (b) are diagrams each showing another example of the display method in the image display device to which the present invention is applied.
- FIGS. 3A and 3B are diagrams showing still another example of the display method in the image display device to which the present invention is applied.
- FIG. 4 is a diagram showing an example of a display method in an image display panel according to the second invention of the present invention.
- FIG. 5 is a diagram showing an example of a panel structure in an image display panel according to the second invention of the present invention.
- FIG. 6 is a diagram for explaining the state of particle groups in the image display panel according to the second invention of the present invention.
- FIGS. 7 (a) to 7 (c) are views showing an example of the method for producing white particles according to the fourth invention of the present invention in the order of steps.
- FIG. 4 is a diagram for explaining a state of particle groups in an image display panel using an image display medium.
- FIGS. 9 (a) and 9 (b) are diagrams for explaining the state of particle groups in an image display panel using a conventional image display medium.
- FIG. 10 is a diagram for explaining the state of particle groups in an image display panel using an image display medium that is a target of the second embodiment according to the fifth invention of the present invention.
- FIG. 11 is a diagram for explaining the state of particle groups in an image display panel using an image display medium that is a target of the second embodiment according to the fifth invention of the present invention.
- FIG. 12 is a view showing a structure of an example of hollow particles used as white particles according to the sixth invention of the present invention.
- FIG. 13 is a diagram showing an example of a state in which flat round shaped particles used for the image display medium according to the eighth invention of the present invention are arranged without gaps on the substrate surface.
- FIG. 14 is a view showing an example of a state in which spherical particles used for an image display medium are arranged with a gap on a substrate surface.
- FIG. 15 is a diagram showing an example of the shape of a partition wall in an image display panel using the image display medium of the present invention.
- an electric field is applied to the image display panel in which the image display medium is sealed between the opposing substrates by some means.
- a low-potential image display medium is attracted by the Coulomb force or the like toward the high-potential electric field direction
- a high-potential image display medium is attracted by the Coulomb force or the like toward the low-potential electric field direction.
- the image display is performed by reciprocating the image display media along the direction of the electric field. Therefore, it is necessary to design an image display panel so that the image display medium moves uniformly and the stability during repetition or storage can be maintained.
- particles or powder fluid used for image display media As for the force applied to the electrode, in addition to the force attracted by the Coulomb force between the particles or the liquid powder, an electric image force with an electrode, an intermolecular force, a liquid bridging force, gravity and the like can be considered.
- two or more kinds of particles 3 having different colors are added from outside the substrates 1 and 2.
- the black particles 3B are moved vertically to the substrates 1 and 2 so that the observer visually recognizes the black particles 3B to display black, or the white particles 3W are visually recognized to the observer to display white. Going.
- partition walls 4 are provided between the substrates 1 and 2, for example, in a lattice shape to define a display cell.
- FIGS. 2 (a) and (b) two or more kinds of particles 3 having different colors (here, white particles 3W and black particles 3B are shown) are combined with the electrode 5 provided on the substrate 1 and the substrate 5.
- the substrate is vertically moved with respect to the substrates 1 and 2, and the black particles 3B are visually recognized by an observer to display black. ⁇ , or the white particles 3 W are made visible to the observer to display white.
- partition walls 4 are provided between the substrates 1 and 2, for example, in a grid pattern to define display cells.
- a voltage is applied between the electrode 5 and the electrode 6 on the particle 3 of the different color (here, the white particle 3 W) on the substrate 1.
- the observer moves the particles 1W in the direction parallel to the substrates 1 and 2 to force the white particles 3W to be seen by the observer and perform white display, or the color of the electrode 6 or the substrate 1 to the observer
- the color of the electrode 6 or the substrate 1 is displayed.
- a partition wall 4 is provided between the substrates 1 and 2 in a lattice shape to define a display cell. .
- a feature of the first invention of the present invention relates to white particles 3 W and white powder fluid using the white particles 3 W among particles used for an image display medium.
- the white particles will be described.
- the feature of the white particles 3W of the present invention consists of a central portion and an outer layer portion covering the central portion, and the central portion has a total reflectance of 70% or more at the interface between the central portion and the outer layer portion,
- the outer layer portion consists of a resin layer in which fine particles of a high refractive material are mixed in at least one or more low refractive materials.
- the reason that the total reflectance of the interface is limited to 70% or more is that if the total reflectance of the interface is less than 70%, the concealment ratio of a small number of particles is low, and the total reflectance of existing particles is low. This is because there is no difference in performance.
- the material of the central portion where the total reflectance at the interface is 70% or more is a metal particle, a particle in which a resin film is coated with a metal film, or a reflective film in which the interface with the outer layer portion is composed of a multilayer film. Certain particles, and the like.
- the metal particles may be solid or hollow, but hollow particles are preferred in that they can be made lighter.
- Examples of the material of the metal particles include materials selected from aluminum, silver, Eckel, chromium, iron, titanium, gold, and alloys thereof.
- Examples of the material of the metal film to be coated on the resin layer include materials selected from aluminum, silver, nickel, chromium, iron, titanium, gold, and alloys thereof.
- the method for producing the metal film to be coated on the resin layer is not particularly limited, but techniques such as plating, vapor deposition, and sputtering can be used.
- techniques such as plating, vapor deposition, and sputtering can be used.
- the design, material, and manufacturing method of a general optical reflection film can be used.
- the relationship between the diameter of the central part and the diameter of the whole particle is not particularly limited! It is preferable that the diameter of the center part be 50 to 95% of the particle diameter. If the diameter of the central part is less than 50% of the particle diameter, the amount of light incident on the interface is relative to the total amount of light incident on one particle. It becomes smaller in size, and there is no difference in performance with existing particles. On the other hand, if the diameter of the central portion exceeds 95% of the particle diameter, scattering in the outer resin layer will not be sufficient, and the specular reflection component will increase. This gives a metallic appearance and cannot be used as an image display medium for a paper-like display. Next, the resin layer of the outer layer constituting the white particles 3W will be described.
- the resin layer in the outer layer is made by kneading and milling the necessary resin, charge control agent, colorant, and other additives, polymerizing from monomers, or using the existing base as resin, It may be coated with a charge control agent, a coloring agent, and other additives.
- a charge control agent e.g., a coloring agent
- examples of the resin, charge control agent, colorant, and other additives are the same as the contents of the particles described below. Further, by using the white particles, a powder fluid (white powder fluid) described later can be obtained.
- At least two or more types of image display media are composed of two types of substantially spherical particles having different colors and charging characteristics and a third particle. By doing so, cohesion and adhesion of particles are prevented, and durability in repeated use is improved.
- FIG. 4 and FIG. 5 are diagrams each showing a configuration of an example of an image display panel according to the second invention of the present invention.
- two types of substantially spherical particles here, white particles 13-1 and black particles 13-2) having different colors and charging characteristics and third particles 13-3 are used.
- a particle group 13 composed of 3 and 3 is sealed between the substrates 11 and 12 as an image display medium, and an electric field is applied to the sealed particle group 13 from the electrodes 15 and 16 so that the substrate 1
- the image is displayed by moving vertically in the direction of 1, 1 and 2.
- this method as shown in Fig.
- the space between the substrates 11 and 12 is divided by partition walls 14 to form a structure with multiple cells, and a group of particles 13 is enclosed in the structure to display images. Panels can also be configured.
- two types of particles 13-1 Since the third particle 13-3 is smaller than 13-2, it cannot be properly shown that the third particle 13-3 exists on the surface of the other particle 13-1. As shown in FIG. 6, the third particles 13-3 are attached to the entire surface of one particle 13-1.
- the two types of substantially spherical particles used in the second invention of the present invention have different colors and charging characteristics.
- the two types of roughly spherical particles can be produced by kneading and pulverizing the required resin, charge control agent, colorant, and other additives, polymerizing from monomers, or converting existing particles into resin and charge control. It may be coated with a coloring agent, a coloring agent, or other additives, but it is important to make the color and charging characteristics of both particles different since they are used in combination.
- the particles In order to make the particles approximately spherical, it is preferable to produce them by polymerization.However, the corners of the particles produced by pulverization are dropped by a mechanical impact force, or the surface is fluidized in an atmosphere at a temperature higher than the melting point. It can also be spherical. Examples of the resin, charge control agent, colorant, and other additives are the same as the contents of the particles described below.
- the third particles used in the second invention of the present invention are particles smaller than the two types of substantially spherical particles, and exist between the two types of substantially spherical particles and play a role of a lubricant. You.
- the average particle diameter of the third particles is from 20 nm to 200 nm, more preferably from 20 nm to 150 nm, and still more preferably from 20 nm! 1100 nm.
- it exceeds 200 ⁇ m the two types of substantially spherical particles are easily separated from each other, and exist between the two particles, and the effect of reducing the cohesive adhesion of the two particles cannot be exhibited.
- it is less than 20 nm the two types of substantially spherical particles are depressed on the surface thereof, and the effect of reducing the cohesion and adhesion of the two particles due to the rolling action cannot be exhibited.
- Materials that can be used as the third particles include metal oxides such as titanium oxide, tin oxide, zinc oxide, tungsten oxide, and iron oxide; nitrides such as titanium nitride; silicon oxide; and titanium compounds. But also the hydrophobized oxidation Fine particles made of metal oxides such as silicon, titanium oxide, tin oxide, zirconium oxide, tungsten oxide, iron oxide, nitrides such as titanium nitride, and fine particles made of titanium compounds, and fine particles made of hydrophobic silicon oxide. It is preferable that
- the hydrophobization is performed by treating with a hydrophobizing agent.
- a hydrophobizing agent the difference between chlorosilane, alkoxysilane, silazane and silylated isocyanate can be used.
- the present inventors have found that agglomerates in particles of the same polarity are caused by the dielectric constant of the particles, and have achieved the third invention of the present invention. That is, when an electric field is formed between the electrodes, the dielectric particles sealed between the substrates provided with the electrodes are affected by the electric field and induce positive and negative charges opposite to each other on the surface of the particles. This phenomenon is called polarization, which causes an electric dipole interaction between the particles and generates an attractive force between the particles. Another property of dielectrics is that they are attracted and concentrated in places with strong electric fields. It can be concluded that both of the above phenomena promote the aggregation of the same kind of particles between the electrodes.
- Relative permittivity ⁇ As a method for solving the above points, in the third invention of the present invention, as a particle material for an image display medium used for image display, , Relative permittivity ⁇ , . ⁇ 5.0, more desirable
- a low-dielectric insulating material with Er 3.0 is selected, and even if a high-dielectric material or a conductive material is used as a particle constituent member, the use of a low-dielectric material as the main material will reduce the overall particle size.
- select the adhering substance so that the particle surface does not have a high dielectric substance or conductive substance, and adjust the adhering amount. By controlling, coagulation between particles of the same polarity is prevented, and good display characteristics are achieved.
- the image display panel used in the image display device of the present invention is composed of two or more types of image display media having different colors as shown in FIG. 1 (a), (b) and FIG. b) See here, the panel used for the display method by moving the white particles 3W and the black particles 3B) vertically with the substrates 1 and 2, and the charged particles 3W of one color (Fig. 3 (a;), (b)) can be applied to any of the panels used for the display method by moving the substrates 1 and 2 in parallel.
- reference numeral 4 denotes a partition wall provided as needed
- reference numerals 5 and 6 denote electrodes provided as needed to apply an electric field to the particles 3.
- a feature of the image display medium of the present invention is that the relative permittivity of the particles 3 is limited.
- Particles can be made by kneading and kneading necessary resins, charge control agents, colorants, and other additives, or by polymerizing from monomers, or by using existing particles as resins, charge control agents, colorants, etc. It may be coated with additives. Examples of the resin, the charge control agent, the colorant, and other additives are the same as the contents of the particles described below.
- the resin as the main material of the particles is made of a low dielectric substance such as polystyrene resin, and the weight of the high dielectric substance is changed by weight (volume).
- (Ratio) Disperse in the main component at 50% or less, and lower the dielectric constant of the whole particle
- Pigments conventionally used when producing black particles carbon black Instead, a low-dielectric insulating black dye is used.
- other conductive substances shall not be used as particle constituent materials. If it is necessary to include a conductive substance, the dielectric constant of the whole particle is reduced by the same formulation as in (1) above. Further, the amount of a conductive substance deposited on the surface of the particle is reduced so as not to impart conductivity to the particle surface. '
- the feature of the fourth invention of the present invention relates to white particles 3W and white powder fluid using the white particles 3W among the particles used for the image display medium.
- the white particles will be described.
- FIGS. 7 (a) to 7 (c) are views showing an example of a method for producing white particles according to the fourth invention of the present invention in the order of steps.
- the white particles of the present invention will be described with reference to FIGS. 7 (a) to 7 (c).
- primary particles of a white pigment are prepared here as an example. .
- titanium oxide 21 pigment titanium oxide is preferably used.
- the average particle diameter of the primary particles may be smaller than the average particle diameter of the white particles to be finally determined, and is preferably in the range of 0.01 to 1.0 ⁇ m as an example. More preferably, the reflectance is in the range of 0.2 to 0.3 / xm, which is the highest.
- the binder 22 is thinly coated on the surface of the primary particles of the prepared titanium oxide 21.
- any material can be used as long as it is a low refractive index material and can be coated.
- PS polystyrene
- PE polyethylene
- PET polyethylene terephthalate
- PC polycarbonate
- POM polyacetal
- Examples of the method include a method in which binder 22 is dissolved in a solvent and sprayed on primary particles of titanium oxide 21; a method of dispersing primary particles of titanium oxide 21 in a solution of binder 22 and spraying; A drying method can be suitably adopted.
- the primary particles of titanium oxide 21 coated with binder 22 on the surface are mixed or stirred in a flowing air stream or mechanically, and agglomerated and formed to a predetermined particle diameter while introducing many fine bubbles. Granulate.
- the primary particles of titanium oxide 21 containing microbubbles 23 and being coated with binder 22 were aggregated or granulated to a predetermined particle size.
- 27 fire particles can be obtained as white particles 24.
- the agglomeration and granulation operations can be performed when the binder 22 is coated on the primary particles of titanium oxide 22.
- Zinc oxide may be used in place of the pigment titanium oxide.
- a powder fluid (white powder fluid) described later can be obtained.
- the image display panel according to the first embodiment of the fifth invention of the present invention is characterized in that one of two types of particles having different charging characteristics and optical reflectance used for at least two or more types of image display media is macroscopically observed on the surface.
- the image display panel according to the second embodiment of the fifth invention of the present invention comprises one of two types of particles having different charging characteristics and optical reflectivity used for at least two or more types of image display media. Particles with macroscopic irregularities on the surface and particles with no macroscopic irregularities on the surface, and particles with electrostatically adhered particles on the surface prevent aggregation and adhesion of particles and are used repeatedly To improve durability.
- FIGS. L (a) and (b) to FIGS. 3 (a) and 3 (b) are diagrams each showing an example of the configuration of an image display panel according to the present invention. Figures 1 (a) and (b) and Figures 2 (a) and (b) In the image display panel according to the present invention shown in FIG.
- particles here, white particles 3W and black particles 3B are used as the two types of image display media having different charging characteristics and optical reflectances.
- An external electric field is applied to the encapsulated particle group 3 (Example of Figs. 1 (a) and (b)) or an electric field is applied from the electrodes 5 and 6 (Figs. 2 (a) and (b) Example of))
- Image display is performed by moving substrates 1 and 2 in the vertical direction.
- a particle group here, white particle group 3W
- a particle group here, white particle group 3W
- An image is displayed by applying an electric field to the encapsulated particle group 3 from the electrodes 5 and 6 and moving the particles in a direction parallel to the substrates 1 and 2.
- the space between the substrates 1 and 2 is divided by a partition wall 4 to have a structure with multiple cells.
- An image display panel can also be configured by enclosing the particle group 3 therein.
- the particles used in the first embodiment of the fifth invention of the present invention have different charging characteristics and optical reflectances contained in at least two or more kinds of image display media as shown in FIGS. 8 (a) and 8 (b).
- There are two types of particles one is a particle 3 W having a shape with macroscopic irregularities on the surface, and the other is a particle 3 B having a shape without macroscopic irregularities on the surface.
- Particles can be prepared by kneading and pulverizing the necessary resin, charge control agent, colorant, and other additives, or polymerizing from monomers, or existing particles by resin, charge control agent, and colorant. It may be coated with other additives.However, since two types are used in combination, it is necessary that one particle surface has macroscopic unevenness and the other particle surface has no macroscopic unevenness. It is vital.
- Fig. 9 (a) between two particles with different charging characteristics, if the surfaces of both particles are smooth and free from macroscopic irregularities, the two particles attract each other because of their different charging characteristics. Since a space cannot be secured between the particles, the particles tend to aggregate and adhere to each other. As shown in Fig. 9 (b), when the surfaces of both particles have macroscopic irregularities, However, the particles are caught between the two particles, so that the particles are likely to aggregate and adhere to each other.
- FIGS. 8 (a) and (b) two particles having different charging characteristics and having different macroscopic surface shapes are used. By doing so, it is possible to secure a space between two particles that attract each other because of their different charging characteristics, and it is possible to prevent aggregation and adhesion of the particles.
- the mother particles 3 having a smooth surface and no macroscopic irregularities as shown in FIG. 8 (b)
- the mother particles 3 having a smooth surface and no macroscopic irregularities as shown in FIG. 8 (b)
- a method is preferably used in which the fine particles 31 are firmly adhered firmly so as not to separate from the base particles 3W.
- the particles used in the second embodiment of the fifth invention of the present invention are, as shown in FIG. 10, two types of particles having different charging characteristics and different optical reflectances contained in at least two or more types of image display media.
- One is a particle 3B having a macroscopic unevenness on the surface, and the other is a particle 3B having no macroscopic unevenness on the surface and having fine particles 32 electrostatically attached to the surface.
- W. Particles can be prepared by kneading and pulverizing the required resin, charge control agent, colorant, and other additives, or by polymerizing from monomers.
- existing particles can be resin, charge control agent, coloring Or two or more additives.However, since two types are used in combination, one particle surface should have macroscopic irregularities and the other particle surface should have no macroscopic irregularities. Is essential. The method for producing these particles is the same as that in the first embodiment.
- Fig. 9 (a) if two particles have different charging characteristics and the surfaces of both particles are smooth and have no macroscopic irregularities, a space cannot be secured between the two particles, as shown in Fig. 9 (a). Agglomeration and adhesion of the particles are likely to occur, and as shown in Fig. 9 (b), when both surfaces of the two particles have macroscopic irregularities, the two particles are caught, and Agglomeration and adhesion of particles tend to occur.
- the two particles having different charging characteristics used in combination have different macroscopic surface shapes, so that the charging characteristics are different. Are different but gradually attract each other. A space can be secured between the two particles, and aggregation and adhesion of the particles can be prevented. This effect is similar to that of the first embodiment. .
- the particles used in the second embodiment of the fifth invention of the present invention in addition to the same effects as in the first embodiment described above, the particles are generated because there is no macroscopic unevenness on the surface as shown in FIG. Even when particles having the same charging characteristics are aggregated, fine particles adhere electrostatically to the surface to secure a space between the particles, and the adhesion of the fine particles is electrostatic and strong. Since it is not adhesion, the fine particles roll on the surface of the particles and play a role as a lubricant between the particles, so that aggregation and adhesion of the particles can be prevented.
- the particles (base particles) having no macroscopic unevenness on the surface are firmly adhered, and the macroscopic depressions on the surface are obtained.
- the fine particles (child particles) used to form the protrusions will be described.
- the average particle diameter of the fine particles is in the range of 201 nm to 200 nm, more preferably, 20 nm to 150 nm, and still more preferably, 20 nm to: L 00 nm. If it exceeds 200 ⁇ m, the adhesion to the particle surface having no macroscopic irregularities on the surface is weakened, and the particles are easily removed from the particle surface without macroscopic irregularities on the surface. become unable. On the other hand, if it is less than 20 nm, the particles do not become macroscopically irregular particles on the surface, but the same as particles without macroscopic irregularities on the surface even if the fine particles are fixed, and the cohesive adhesion of the two particles The reduction effect cannot be exhibited.
- the charge polarity of the fine particles may be the same as that of the particles (matrix particles) having no macroscopic unevenness on the surface, but it is important that they are firmly fixed to the base particles. Thus, fine particles (child particles) firmly adhere to the surface of the particles (base particles) having no macroscopic unevenness on the surface.
- materials that can be used as the fine particles include titanium oxide and tin oxide And metal oxides such as zirconium oxide, tungsten oxide and silicon oxide, nitrides such as titanium nitride, silicon oxide, titanium compounds, and the like.
- metal oxides such as zirconium oxide, tungsten oxide and silicon oxide, nitrides such as titanium nitride, silicon oxide, titanium compounds, and the like.
- hydrophobized silicon oxide, titanium oxide, and oxide Fine particles composed of metal oxides such as tin, zirconium oxide, tundatin oxide, and iron oxide, nitrides such as titanium nitride, and fine particles of a titanium compound are preferable, and fine particles composed of hydrophobic silicon oxide are preferable.
- the hydrophobization is performed by treating with a hydrophobizing agent.
- a hydrophobizing agent any of chlorosilane, anorecoxy silane, silazane, and silylated isocyanate can be used. More specifically, methyltrichlorosilane, dimethyldichlorosilane, trimethyl silane, methyltrimethoxysilane, dimethyldimethoxysilane, methyltriethoxysilane, dimethylethoxysilane, isobutyltrimethoxysilane, decyltrimethoxysilane, hexamethyldisilazane, ter- Examples thereof include silane, butylinoletrichlorosilane, bininoletrimethoxysilane, and burtriethoxysilane.
- fine particles can be firmly and firmly fixed to the surface of the particle (base particle) without macroscopic irregularities on the surface.
- the fine particles used in the second embodiment of the fifth invention of the present invention are smaller than the two types of particles having different colors and different charging characteristics, and are macroscopic on the surface among the two types of particles having different colors and different charging characteristics.
- Lubricant between particles that have no macroscopic irregularities on the surface (between particles that have the same charging characteristics) among the two types of particles that have different colors and different charging characteristics by electrostatically adhering to the surface of the particles without the roughness. It plays a significant role.
- the average particle diameter of the fine particles is from 20 nm to 200 nm, more preferably 20 nm. 1150 nm, more preferably 20 nm ⁇ ; and L 100 nm. If it exceeds 200 ⁇ m, it is difficult to electrostatically adhere to the particle surface having no macroscopic unevenness on the surface, and the particle is present between the two particles and the effect of reducing the cohesive adhesion of the two particles cannot be exhibited. On the other hand, if it is less than 20 nm, the electrostatic adhesion becomes too strong, and the effect of a lubricant on the particle surface is not exerted, so that the cohesion between two particles having the same charging characteristics is reduced. The effect cannot be exhibited. '
- the charging polarity of the fine particles is opposite to the polarity of the particles having no macroscopic unevenness on the surface among the two types of particles having different colors and charging characteristics, and the fine particles electrostatically have no macroscopic unevenness on the surface. Attaches to surface. If the particles have the same polarity as the particles having no macroscopic irregularities on the surface, the particles will electrostatically adhere to the surface of the particles having macroscopic irregularities on the surface, and the effect of reducing the cohesive adhesion of the two particles cannot be exhibited.
- Materials that can be used as the fine particles include metal oxides such as titanium oxide, tin oxide, zirconium oxide, tungsten oxide, and iron oxide; nitrides such as titanium nitride; silicon oxide; and titanium compounds. And fine particles made of metal oxides such as hydrophobized silicon oxide, titanium oxide, tin oxide, zirconium oxide, tungsten oxide, iron oxide, nitrides such as titanium nitride, and titanium compounds.
- the fine particles are made of hydrophobic silicon oxide.
- Hydrophobization is achieved by treating with a hydrophobizing agent, and any of chlorosilane, alkoxysilane, silazane, and silylated isocyanate can be used as the hydrophobizing agent.
- a hydrophobizing agent any of chlorosilane, alkoxysilane, silazane, and silylated isocyanate can be used as the hydrophobizing agent.
- a feature of the sixth invention of the present invention relates to white particles 3 W and white powder fluid using the white particles 3 W among particles used for an image display medium.
- the white particles will be described.
- the white particles according to the present invention are characterized in that, when produced by the kneading and pulverizing method, hollow particles replace a part of the white pigment mixed to make the base resin white.
- the production method is a kneading and pulverizing method.
- the polymerization method it is necessary to aggregate the monomer and the pigment in a liquid at the time of producing the polymer particles, but even if an attempt is made to use hollow particles instead of the pigment, This is because the hollow particles float in the liquid in the liquid, and the hollow particles cannot be used.
- the base resin, white pigment (all or partly hollow particles), CCA (charge control agent), various fillers (fluidity-imparting agent, adhesion prevention) And the like) are kneaded with a twin-screw extruder or a plastomill, and the resulting lumps and pellets are ground to a predetermined particle size.
- a freeze pulverization method or various pulverization methods can be used.
- a resin such as PMMA (polymethyl methacrylate), PC (polycarbonate), acrylic urethane, acrylic, or the like can be suitably used as the base resin.
- the white pigment titanium oxide, zinc oxide, zirconium oxide, or the like can be preferably used as the white pigment.
- FIG. 12 is a diagram showing the structure of an example of the hollow particles used in the white particles of the present invention.
- the hollow grain core 41 is composed of an internal void part 42 and a spherical highly crosslinked polymer layer 43 formed so as to surround the entire outer periphery of the void part 42.
- the highly crosslinked polymer layer 43 crosslinked styrene-acryl can be suitably used.
- the hollow particles 41 are hollow such as light scattering properties and heat insulating properties. And characteristics due to being a crosslinked polymer such as heat resistance and solution resistance. In particular, light is scattered by the air in the highly crosslinked polymer layer 43 and the air gap 42 to exert a hiding effect, and white particles can be obtained by replacing a part of the white pigment.
- the white particles according to the sixth invention of the present invention are configured by filling a white pigment and hollow particles into a resin serving as a base.
- a white pigment which is a white pigment
- the whiteness of white particles showed the maximum at about 200 parts by weight of titanium oxide with respect to 100 parts by weight of the base resin. If the added amount of titanium is 300 parts by weight, kneading becomes difficult, and the whiteness decreases due to poor dispersion.
- the whiteness is improved as compared with the case of filling 200 parts by weight of titanium oxide.
- the kneading properties are improved, and higher filling is possible than when only titanium oxide is filled. Further, by using these white particles, a powder fluid (white powder fluid) described later can be obtained.
- the display panel in which at least two or more types of image display media are sealed between opposing substrates is charged on the substrate by some means. And an electric field acts between the substrates.
- the low potential charged image display medium is attracted toward the high potential substrate portion by Coulomb force or the like, and the high potential charged image display medium is directed toward the low potential substrate portion.
- the images are attracted by force and the image display medium reciprocates between the two substrates to display an image. Therefore, it is necessary to design a display panel so that the image display medium can move uniformly and maintain stability when the image is displayed repeatedly, repeatedly, or stored.
- FIGS. 1 (a) and 1 (b) to 3 (a) and 3 (b) are diagrams each showing a configuration of an example of an image display panel using the particles according to the seventh invention of the present invention as an image display medium.
- the image display panel of the present invention shown in FIGS. L (a) and (b) and FIGS. 2 (a) and (b) In this case, particles (here, white particles 3W and black particles 3B) are encapsulated between substrates 1 and 2 as two types of image display media with different charging characteristics and optical reflectivity, and the encapsulated particles are encapsulated.
- an electric field is applied externally to 3 (examples in Figs.
- FIGS. 3 (a) and 3 (b) a particle group (here, a white particle group 3W) is sealed between the substrates 1 and 2 as one kind of image display medium. Then, an image is displayed by applying an electric field from the electrodes 5 and 6 to the encapsulated particle group 3 and moving the particles in a direction parallel to the substrates 1 and 2.
- a partition wall 4 to form a structure with multiple cells.
- An image display panel can be constructed by enclosing the particle group 3 therein.
- a feature of the seventh invention of the present invention resides in the structure of the particles used for the image display medium in the image display panel having the above structure. That is, a thermosetting resin is used as the base resin of the particles, and a resin material containing the thermosetting resin is kneaded, then subjected to a thermal crosslinking reaction, and then pulverized to obtain particles.
- a thermosetting resin that has been subjected to a thermal crosslinking reaction in this way, an improvement in heat resistance of about 30 ° C. can be seen in comparison with an example using a conventional thermoplastic resin as a base resin.
- thermosetting resin is a polyester resin generally called polyurethane and a block isocyanate (more specifically, a polyester resin having an OH terminal + a block isocyanate having three or more functional groups).
- Other combinations that can be thermally crosslinked at a higher temperature than the temperature at which the resin material is kneaded after kneading include alkyd resin + melamine curing agent system, epoxy resin + amine curing agent system, and rare resin + formaldehyde. .
- pigments titanium oxide, carbon black, etc.
- CCA charge control agents
- organotin catalysts, etc. are appropriately selected and used as in the case of conventional particles. can do.
- a compound is produced by kneading a thermosetting resin as a base material and a resin material comprising other materials such as a pigment, a charge control agent, an organotin catalyst and the like.
- the compound can be subjected to a crosslinking reaction by applying X temperature (temperature higher than the temperature at the time of kneading) for a predetermined time, and then finely pulverized by a jet mill to obtain particles.
- the feature of the image display panel according to the eighth invention of the present invention is that at least one particle shape of two types of particles having different charging characteristics and optical reflectances contained in at least two or more types of image display media. Is a flat round shape.
- FIG. 13 shows a state in which flat round particles are arranged on the substrate surface without gaps
- FIG. 14 shows a state in which spherical particles are arranged on the substrate surface with gaps
- the particles used in the eighth invention of the present invention are two kinds of particles having different charging characteristics and optical reflectances contained in at least two or more kinds of image display media, and at least one of the particles has a flat round shape.
- Particles. The particles are made by kneading the necessary resin, charge control agent, colorant, and other additives, pulverizing the thin sheet first, and exposing the crushed pieces to a temperature higher than the melting point of the resin. Melt the corners of the crushed pieces and roll them. Further, it can be produced by polymerization from a monomer, but it is difficult to obtain flat round particles having a particle diameter (average particle diameter: 0.1 to 50111) suitably used in the present invention. Examples of the resin, the charge control agent, the colorant, and other additives are the same as the contents of the particles described below.
- the feature of the image display panel according to the ninth invention of the present invention is that the relationship between the particle diameters of two types of particles (dark and dark particles and light and light particles) contained in the image display medium and having different color and charging characteristics.
- the average particle size of the light and bright particles is Dbright, and the dark and dark particles are This is the point expressed by Ddark ⁇ Dbright, where the average particle size of Ddark is Ddark.
- Ddark ⁇ Dbright the average particle size of Ddark
- the degree of the relationship between Ddark and Dbright cannot be clearly specified, but a slight difference is sufficient. If the difference is too large, the result is rather bad. Therefore, it is preferable to set the range to 1 / Dbright / Ddark / 2. Here, it is preferable to set Dbright / Ddark ⁇ 2. If there is a difference of more than two times in the particle diameter, dark and dark particles with a small particle diameter are located in the gaps where light and bright particles with a large particle diameter are properly arranged. This may cause a problem such as a decrease in whiteness due to the presence of dark and dark colored particles in the gaps between the arranged light and bright colored particles.
- Particles having different colors and charging characteristics used in the present invention are particles in which one particle group is made up of dark and dark colored particles, and the other particle group is made up of light and bright colored particles.
- the particles can be prepared by kneading and pulverizing and classifying necessary resins, charge control agents, coloring agents and other additives, or by polymerizing and classifying from monomers. Examples of the resin, the charge control agent, the colorant, and other additives are the same as the contents of the particles described below.
- a feature of the tenth invention of the present invention resides in the structure of the particles used in the image display medium used in the image display panel having the above structure. That is, the chargeability is controlled by blending a metal oxide or a fatty acid metal salt compound with the base resin of the particles. By mixing the metal oxide or the fatty acid metal salt conjugate with the base resin in this way, the desired charge control can be performed as compared with the case where the charge control could not be conventionally performed. be able to.
- the metal oxide (MOx, where M: metal element, O: oxygen, and X: O / M ratio) to be mixed with the base resin of the particles any of the examples of metal oxides conventionally known as metal oxides can be used. can also be utilized, to illustrate, there are MgO, ZnO, etc. A 1 2 0 3, S i 0 2, S n 0 2, F e 3 0 4, F e 2 ⁇ 3.
- M a metal element
- m, n, y, and z are integers, and 4 ⁇ m ⁇ 22) can be any of the examples conventionally known as fatty acid metal salt compounds.
- the poling electronegativity of the metal element (M) ion is 0.79 ⁇ % ⁇ !.
- the metal element may be any one of Mg, Zn, Ca, Li, Zr, Al, Ni, Cu, Ba, and Ti.
- the Pauling electronegativity% of the ion of the metal element (M) is 0.79 ⁇ z ⁇ 1.91. If the electronegativity% is 0.79 or less, the charge amount becomes small.
- the image display medium does not reverse when the image display panel is configured because it is too high, and when the electronegativity X is 1.91 or more, the charge amount becomes too low to configure the image display panel. This is because the image display medium does not turn over again.
- the poling electronegativity ⁇ ⁇ ⁇ of the metal element (M) ion is 1.50 ⁇ 2.58.
- the metal element is one of Fe, Ti, Cu, Si, Sb, W, Sn, Ge, and Co.
- the Pauling electronegativity of the metal element (M) ion is It is preferable that 1.50 ⁇ 2.58 is satisfied when the electronegativity ⁇ is less than 1.50 when the charge amount becomes too low and the image display panel is formed. If the image display medium does not reverse and the electronegativity X is 2.58 or more, the charge amount becomes too high and the image display medium does not reverse when the image display panel is formed. ⁇
- the configuration of the image display device common to the first to tenth aspects of the present invention will be described in the order of the substrate, the electrode, and the partition wall, and the particle group and the powder fluid will be described.
- the substrate As for the substrate, at least one of the substrates is a transparent substrate 2 from which the color of the image display medium can be confirmed from the outside of the apparatus, and a material having high visible light transmittance and high heat resistance is preferable.
- Substrate 1 may be transparent or opaque. Examples of substrate materials include polymer sheets such as polyethylene terephthalate, polyethersulfone, polyethylene, polycarbonate, polyimide, and acrylic, and flexible sheets such as metal sheets, and flexible sheets such as glass and quartz. An inorganic sheet having no properties can be used.
- the thickness of the substrate is preferably from 2 to 500 / im, more preferably from 5 to 200 ⁇ .If the thickness is too small, it is difficult to maintain the strength and uniformity of the spacing between the substrates. When the thickness is larger than 0 m, there is an inconvenience when a thin image display device is formed.
- the electrodes 6 provided on the substrate 2 side which is on the viewing side and need to be transparent are formed of a transparent and patternable conductive material, for example, indium oxide, aluminum, Examples thereof include metals such as gold, silver, and copper, and conductive polymers such as polyaniline, polypyrrole, and polythiophene. Examples of the forming method include vacuum evaporation and coating.
- the thickness of the electrode may be 3 to 100 nm, preferably 5 to 400 nm, as long as conductivity can be ensured and there is no problem with light transmittance.
- the material and thickness of the electrode 5 provided on the substrate 1 side are the same as those of the electrode 6 described above, but need not be transparent.
- the external voltage input in this case is DC Alternatively, an alternating current may be superimposed.
- the shape is appropriately set as appropriate according to the type of the image display medium involved in the display, and is not particularly limited, but the width of the partition wall is 2 to 100 m, preferably 3 to 100 m.
- the height of the septum is adjusted to 50 m, and the height of the septum is adjusted to 10 to 500 ⁇ , preferably to 10 to 200 m.
- a two-rib method in which a rib is formed on each of the opposing substrates and then joined, or a one-rib method in which the rib is formed only on one substrate is conceivable. In the present invention, any of the methods is suitably used. '
- the display cells formed by the ribs formed of these ribs have a rectangular, triangular, line, circular, or hexagonal shape as viewed from the plane of the substrate.
- a honeycomb shape or a mesh shape is exemplified. It is better to make the part (area of the display cell frame) corresponding to the cross section of the partition wall visible from the display side as small as possible, so that the sharpness of the image display increases.
- the method of forming the partition include a screen printing method, a sand plast method, a photolithographic method, and an additive method. Among them, a photolithography method using a resist film is preferably used.
- the particles can contain a charge controlling agent, a coloring agent, an inorganic additive, and the like, if necessary, in a resin as a main component, as in the conventional case.
- a charge controlling agent e.g., a coloring agent, an inorganic additive, and the like, if necessary, in a resin as a main component, as in the conventional case. Examples of resins, charge control agents, coloring agents, and other additives are described below.
- resins include urethane resins, rare resins, acrylic resins, polyester resins, acrylic urethane resins, acrylic urethane silicone resins, acrylic urethane fluororesins, acrylic fluororesins, silicone resins, acrylic silicone resins, epoxy resins, and polystyrene resins. , Styrene-acrylic resin, polyolefin resin, butyral resin, polyvinylidene chloride resin, melamine resin, phenol resin, fluororesin, polycarbonate resin, polysulfone resin, polyether resin, polyamide resin, etc. You can also.
- acrylic urethane resin acrylic silicone resin, acryl fluorine resin, acryl urethane silicone resin, acrylic urethane fluorine resin, fluorine resin, and silicone resin are preferable.
- the charge control agent is not particularly limited, but examples of the charge control agent include metal complexes of salicylic acid, metal-containing azo dyes, metal-containing (including metal ions and metal atoms) oil-soluble dyes, and quaternary. Examples include an ammonium salt-based compound, a liquixallene compound, a boron-containing compound (boron benzylate complex), and a nitroimidazole derivative. Examples of the positive charge control agent include a Nig mouth dye, a triphenylmethane compound, a quaternary ammonium salt compound, a polyamine resin, and an imidazole derivative.
- metal oxides such as ultrafine silica, ultrafine titanium oxide and ultrafine alumina, nitrogen-containing cyclic compounds such as pyridine and derivatives and salts thereof, various organic pigments, resins containing fluorine, chlorine, nitrogen, etc.
- a charge control agent various kinds of organic or inorganic pigments and dyes as exemplified below can be used.
- black colorant examples include carbon black, copper oxide, manganese dioxide, phosphorus black, and activated carbon.
- C.I. Pigment Blue 15 3
- C.I. Pigment Blue 1-15 Navy Blue
- Cobalt Punolay Alkaline Vunoray Lake, Victoria Pull Lake
- Phthalocyanine Blue Metal-free Phthalocyanine Blue
- Phthalocyan blue partially chlorinated products, First Sky Blue, Indaslen Blue BC and others.
- Red colorants include Bengala, Cadmium Red, Lead Tan, Mercury Sulfide, Cadmium, H-Mount Red 4R, Litho / Lered, Pyrazolone Red, Watched Greed, Calcium Salt, Lake Red D, Brilliant Carmine 6 B, Eo Sin Lake, Rhodamine Lake B, Alizarin Lake, Brilliant Carmine 3B, C.I.
- Yellow colorants include: graphite, zinc yellow, cadmium yellow, yellow iron oxide, mineral lanole first yellow, nickele titanium yellow, navel yellow, naphthyl yellow S, hanzeyello G, hanzeyello 10G, benzidine yellow One G, Benzijin Yellow GR, Kinolin Yellow Lake, Permanent Yellow I NCG, Tartrazine Lake, C.I. Green colorants include chrome green, chromium oxide, pigment green B, C.I. pigment green 7, malachite green lake, and huainanoreiero mono green G '.
- Orange colorants include red-yellow molybdenum orange and permanent orange
- GTR pyrazolone orange, ba / lecan orange, Indaslen brilliant range RK :, benzidine orange G, induslen prilian orange GK :, CI.
- purple colorants examples include manganese purple, First Violet B, and methyl violet lettuce.
- white colorants include zinc white, titanium oxide, antimony white, and zinc sulfide.
- extenders include barite powder, barium carbonate, clay, silica, white carbon, talc, and alumina white.
- Various dyes such as basic, acidic, disperse, and direct dyes include Nigguchi Shin, Methylene Blue, Rose Bengal, Quinoline Yellow, and Ultramarine Pull.
- inorganic additives examples include titanium oxide, zinc oxide, zinc sulfide, antimony oxide, calcium carbonate, lead white, talc, silica, calcium silicate, alumina white, cadmium yellow, cadmium red, cadmium orange, and titanium yellow. , Navy blue, ultramarine, cobalt benoray, konoku noreto green, cobalt violet, iron oxide, carbon black, manganese ferrite black, cobalt ferrite black, copper powder, anore powder. These pigments and inorganic additives can be used alone or in combination of two or more. Of these, carbon black is particularly preferred as the black pigment, and titanium oxide is preferred as the white pigment.
- the particles of the present invention have an average particle diameter d (0.5) in the range of 0.1 to 50 ⁇ m, and are preferably uniform and uniform. If the average particle diameter d (0.5) is larger than this range, the display will lack sharpness. If the average particle diameter d (0.5) is smaller than this range, the cohesion between the particles will be too large to hinder the movement of the particles. Become.
- the particle size distribution Span represented by the following formula is set to less than 5, preferably less than 3.
- the ratio of d (0.5) of the particle having the smallest diameter to d (0.5) of the particle having the largest diameter is 50 or less, preferably 1 It is important to keep it below 0. Even if the particle size distribution Span is reduced, particles with different charging characteristics move in opposite directions, so that the particle sizes are close to each other so that each particle can easily move in the opposite direction by an equivalent amount. It is preferable that this is within this range.
- the above-mentioned particle size distribution and particle size can be determined by a laser diffraction / scattering method or the like.
- a laser beam is irradiated on the particles to be measured, a light intensity distribution pattern of spatially diffracted Z scattered light is generated, and since this light intensity pattern has a correspondence with the particle size, the particle size distribution is smaller.
- the particle size and the particle size distribution in the present invention are obtained from a volume-based distribution. Specifically, particles are injected into a nitrogen gas flow using a Mastersizer2000 (Malvern Instruments Ltd.) measuring instrument, and the particles are analyzed using the attached analysis software (software based on volume-based distribution using Mie theory). Measurement of diameter and particle size distribution can be performed.
- Mastersizer2000 Malvern Instruments Ltd.
- the ⁇ 'Ut of the particles naturally depends on the measurement conditions, but the charge amount of the particles used for the image display medium in the image display panel is almost the initial charge amount, contact with the P wall, contact with the substrate, progress It was found that it depends on the charge decay with time, and in particular, the saturation value of the charging behavior of the particles is the dominant factor.
- the “powder fluid” in the present invention is a substance in an intermediate state between a fluid and a particle which exhibits fluidity by itself without using the power of gas or liquid.
- a liquid crystal is defined as an intermediate phase between a liquid and a solid, and has fluidity, which is a characteristic of liquid, and anisotropy (optical properties), which is a characteristic of solid (Heibonsha: Encyclopedia) ).
- anisotropy optical properties
- the definition of a particle is an object having a finite mass, even if it is negligible, and is said to be affected by gravity (Maruzen: Encyclopedia of Physics).
- the particles also have a special state of gas-solid fluidized bed or liquid-solid fluid, and when gas flows from the bottom plate to the particles, an upward force acts on the particles corresponding to the velocity of the gas, When this force balances with gravity, a material that can easily flow like a fluid is called a gas-solid fluidized bed, and a fluidized fluid is also called a liquid-solid fluid. Yes (Heijinsha: Encyclopedia). In this way, gas-solid fluidized bed and liquid-solid fluid It is in the state using. According to the present invention, it has been found that a material in a state of exhibiting fluidity can be specifically produced without using the power of such a gas or the power of a liquid, and this is defined as a powder fluid.
- the powder fluid used for the image display medium in the present invention is an intermediate state having both characteristics of particles and liquid, as in the definition of liquid crystal (intermediate phase between liquid and solid). It is a material that is extremely unaffected by the characteristic gravity and exhibits a unique state of high fluidity.
- a substance can be obtained in an aerosol state, that is, a dispersion system in which a solid or liquid substance is stably suspended as a dispersoid in a gas, and the solid substance is dispersed in the image display device of the present invention. It is assumed that.
- the image display panel which is the object of the present invention has a high fluidity in an air port sol state in which solid particles are stably suspended as a dispersoid in a gas as an image display medium between at least one of the transparent substrates facing each other.
- the powdered fluid shown is sealed, and such a powdered fluid can be easily and stably moved by Coulomb force or the like when a low voltage is applied.
- the powder fluid used in the image display medium of the present invention is an intermediate state between the two, which exhibits fluidity by itself and has both the properties of fluid and particles, without using the power of gas or liquid. Is a substance.
- This powder fluid can be in particular in an aerosol state, and is used in the image display device of the present invention in a state where a solid substance floats relatively stably as a dispersoid in a gas.
- the range of the state of the aerosol is preferably twice or more, more preferably 2.5 times or more, particularly preferably 3 times or more, the apparent volume of the powder fluid at the time of maximum suspension.
- the upper limit is not particularly limited, but is preferably 12 times or less. If the apparent volume at the time of the maximum suspension of the powder fluid is smaller than twice that of the non-floating state, it will be difficult to control the display.If it is larger than 12 times, the powder fluid will be missed when it is sealed in the device. Inconvenience in handling such as occurs.
- the apparent volume at maximum suspension is measured as follows. That is, the powder flows into a closed container through which the powder fluid can be seen.
- a polypropylene container with a diameter (inner diameter) of 6 cm and a height of 10 cm (trade name: Iboy: manufactured by Az-One Co., Ltd.) has a volume equivalent to 1/5 of the volume of powder fluid when not suspended. Fill the powder fluid, set the container on a shaker, and shake at a distance of 6 cm at 3 reciprocations / sec for 3 hours. The apparent volume immediately after stopping shaking is the apparent volume at the time of maximum suspension.
- the change over time of the apparent volume of the powder fluid satisfies the following expression.
- V 5 is the apparent volume of 5 minutes after the maximum floating (cm 3)
- V 10 indicates the apparent volume after 10 minutes from the time of maximum floating (cm 3).
- time change V 1 of the apparent volume of the liquid powder () / V 5 is rather preferably is greater than 0.85, greater than 0.9 is particularly preferred.
- V lt) / V 5 is 0.8 or less, it is the same as the case using ordinary so-called particles, and the effects of high-speed response and durability as in the present invention cannot be secured.
- the average particle diameter (d (0.5)) of the particulate matter constituting the powder fluid is preferably 0.1 to 20 ⁇ , more preferably 0.5 to 15 / im, and particularly preferably 0.5 to 15 / im.
- the average particle size (d (0.5)) of the particulate matter constituting the powder fluid is the same as d (0.5) in the following particle size distribution Span.
- the particle material constituting the powder fluid preferably has a particle size distribution Span represented by the following formula of less than 5, and more preferably less than 3.
- Particle size distribution Span (d (0.9) _d (0.1)) / d (0.5) where d (0.5) is 50% of the particulate matter constituting the powder fluid is larger than this , 50% smaller particle size! ⁇ ⁇ m, d (0.1)
- the above particle size distribution and particle size can be determined by laser diffraction Z scattering method or the like.
- a laser beam is irradiated on the powder fluid to be measured, a spatial pattern of light intensity distribution of diffracted / scattered light is generated, and since this light intensity pattern has a correspondence with the particle size, the particle size and the particle size are determined.
- the distribution can be measured.
- the particle size and the particle size distribution are obtained from the volume-based distribution. Specifically, using a Mastersizer2000 (Malvern Instruments Ltd.) measuring instrument, charge the powder fluid into a nitrogen stream and use the attached analysis software (software based on volume-based distribution using Mie theory). Measurements can be made.
- Powders can be made by mixing the necessary resin, charge control agent, colorant, and other additives, kneading and milling, or polymerizing from monomers, and converting existing particles into resin, charge control agent, colorant, etc. It may be coated with an additive.
- the resin, charge control agent, colorant, and other additives constituting the powder fluid will be exemplified.
- resins include urethane resin, acrylic resin, polyester resin, urethane-modified acrylic resin, silicone resin, nylon resin, epoxy resin, styrene resin, petital resin, vinylidene chloride resin, melamine resin, phenolic resin, fluorine resin, etc. It is also possible to mix two or more kinds. Particularly, from the viewpoint of controlling the adhesion to the substrate, acrylic urethane resin, acrylic urethane silicone resin, acrylic urethane fluororesin, urethane resin, and fluororesin are preferred.
- Examples of the charge control agent include, in the case of imparting a positive charge, a quaternary ammonium salt-based conjugate, an egrosine dye, a triphenylmethane-based compound, and an imidazole derivative.
- Examples include metal-containing azo dyes, salicylic acid metal complexes, and nitridazole imidazole derivatives.
- As the coloring agent various kinds of organic or inorganic pigments and dyes as exemplified below can be used.
- black colorants examples include carbon black, copper oxide, manganese dioxide, aniline black, and activated carbon.
- Blue colorants include CI Pigmentable 15: 3, C.I. Pigmented Tonole 15, Navy Blue, Cobalt Blue, Al Ripple Rake, Victoria Bull Rake, Phthalocyanine Bull, Metal-Free Phthalocyanine Punolay, Phthalocyan Samples include partially chlorinated products, First Sky Pull 1, Indasulen Blue BC, etc.
- Red colorants include Bengala, Cadmium Red, Lead Tan, Mercury Sulfide, Cadmium, Permanent Red 4R, Lisorone Red, Pyrazolone Red, Watching Red, Canolecidium Salt, Lake Red D, Prilianto Carmine 6B, Eo Shin Lake, Rhodamine Lake B, Alizarin Lake, Priliant Carmine 3
- Yellow colorants include: graphite, zinc yellow, cadmium yellow, yellow iron oxide, mine lanoreferth toyello, nickele titanium titanium yellow, neve noreyellow, naphtho-noleyello S, nonzyaello G, nonzyaello 10G, venzijin yellow 1G, Benzijin Yellow GR, Quinoline Yellow Lake, No ⁇ 0 —Manent Yellow One NCG ⁇ Tartradin Lake, C.I.
- Green colorants include chrome green, chromium oxide, pigment green B,
- Orange colorants include red lead, molybdenum orange, permanent orange GTR, pyrazolone orange, vanorecan orange, induslenburi liantorange RK :, benzidine orange G, induslenburi liant orange GK, C.I. Orange has 31 mag.
- Examples of the purple colorant include manganese purple, first violet B, and methinore biolette lake.
- white colorants include zinc white, titanium oxide, antimony white, and sulfurous acid.
- extender pigments include barite powder, barium carbonate, clay, silica, white carbon, talc, and alumina white.
- Various dyes such as basic, acidic, dispersible, and direct dyes include egrosin, methylene blue, rose bengal, quinoline yellow, and ultramarine pull.
- inorganic additives include titanium oxide, zinc oxide, zinc sulfide, antimony oxide, calcium carbonate, lead white, talc, silica, calcium silicate, alumina white, cadmium yellow, cadmium red, cadmium orange, and titanium yellow. , Navy blue, ultramarine, konore violet, konore green, konore violet, iron oxide, black carbon black, manganese ferrite black, cobalt ferrite black, copper powder, aluminum powder and the like.
- pigments and inorganic additives can be used alone or in combination.
- carbon black is particularly preferred as the black pigment
- titanium oxide is preferred as the white pigment.
- inorganic fine particles having an average particle size of 20 nm or more and 100 nm or less, preferably 20 nm or more and 80 nm or less, on the surface of the particle material constituting the powder fluid. Further, it is appropriate that the inorganic fine particles are composed of two or more kinds of fine particles. Further, it is appropriate that the inorganic fine particles are treated with silicone oil.
- the inorganic fine particles silicon dioxide (silica), zinc oxide , Aluminum oxide, magnesium oxide, cerium oxide, iron oxide, copper oxide and the like.
- the method of fixing the inorganic fine particles is important.
- a device such as a hybridizer (manufactured by Nara Kikai Seisakusho Co., Ltd.) or a mechanofusion (manufactured by Hosokawa Micron Co., Ltd.) under certain limited conditions (for example, treatment) Only at time)
- a powder fluid showing a sol state in the air port can be produced.
- it is important to control the gas in the space surrounding the image display medium between the substrates, which contributes to the improvement of display stability.
- the relative humidity at 25 ° C of the gas in the void portion may be 60 ° / 0 RH or less, preferably 50% RH or less, and more preferably 35% RH or less. is important.
- the gap portion is defined as a portion between the opposing substrate 1 and substrate 2, the electrodes 5 and 6 (when the electrodes 5 and 6 are present), the image display medium (particles or particles). Excluding the portion occupied by the powdered fluid 3), the portion occupied by the partition 4 (if the partition 4 is present), and the gas portion in contact with the so-called image display medium, excluding the device seal portion.
- the type of gas in the void portion is not limited as long as it is in the humidity range described above, but dry air, dry nitrogen, dry argon, dry helium, dry carbon dioxide, dry methane, and the like are suitable.
- This gas must be sealed in a device so that the humidity is maintained. For example, filling the image display medium, assembling the substrate, etc. under a predetermined humidity environment, It is important to provide a sealing material and a sealing method to prevent intrusion.
- the distance between the substrates in the image display panel included in the image display device of the present invention is not particularly limited as long as the image display medium can be moved and the contrast can be maintained, but is usually 10 to 500 ⁇ , preferably 10 to Adjusted to 200 ⁇ .
- the volume occupancy of the image display medium in the space between the opposing substrates is preferably 5 to 70%, more preferably 5 to 60%. If it exceeds 70%, the image display medium Embodiments according to the first to tenth aspects of the present invention will be described below in order. ⁇ Example of First Invention>
- Aluminum spheres with an average particle size of 7.0 ⁇ were used as the 'central' core.
- the total reflectivity of the surface of the aluminum sphere that constitutes the central part used (corresponding to the interface between the central part and the outer layer part) was 85%.
- An existing white material was coated on the aluminum sphere serving as the central portion using Agromaster (manufactured by Hosokawa Micron Corporation) to form an outer layer portion, and the white particles of the present invention were obtained.
- the white material is acrylic urethane resin E AU53B (manufactured by Asia Kogyo Co., Ltd.) ZIPDI cross-linking agent Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.), titanium oxide 10 phr, charge control agent Bontron E 8 9 (manufactured by Orient Chemical Co., Ltd.) 2 phr was added, kneaded, and then pulverized and classified by a jet mill to prepare.
- acrylic urethane resin E AU53B manufactured by Asia Kogyo Co., Ltd.
- ZIPDI cross-linking agent Ethacell Hardener HX manufactured by Asia Kogyo Co., Ltd.
- titanium oxide 10 phr titanium oxide 10 phr
- charge control agent Bontron E 8 9 manufactured by Orient Chemical Co., Ltd. 2 phr was added, kneaded, and then pulverized and classified by a jet mill to prepare.
- the average particle size of the obtained white particles was 9.0 ⁇ , and the surface charge density was 160 ⁇ CZm 2 .
- the luminance ratio of the white particles of the present invention was improved by 5% compared to the luminance ratio of the existing basic white particles. .
- Aluminum deposited on a PMM sphere having an average particle diameter of 5.0 im by 500 nm was used as a central portion serving as a nucleus.
- the total reflectance of the surface (corresponding to the interface between the center portion and the outer layer portion) of the aluminum deposited film constituting the center portion used was 82%.
- This central portion was coated with an existing white material using Agromaster (manufactured by Hosokawa Micron Corporation) in the same manner as in Example 1 to prepare an outer layer portion, and the white particles of the present invention were obtained.
- the average particle diameter of the obtained white particles is 8.0 ⁇ m, and the surface charge density is 150 Z CZm 2 .
- the luminance ratio of the white particles of the present invention was improved by 4% as compared with the luminance ratio of the existing white particles. .
- a core obtained by alternately depositing 80 nm-thick titanium oxide and 100 nm-thick silicon oxide on PC spheres having an average particle diameter of 5.0 m was used as a core.
- the total reflectance of the surface of the deposited film constituting the central portion used (corresponding to the interface between the central portion and the outer layer portion) was 91%.
- an existing white material was coated on this central portion using Agromaster (manufactured by Hosokawa Micron Corporation) to form an outer layer portion, and white particles of the present invention were obtained.
- the average particle diameter of the obtained white particles was 7.0 ⁇ m, and the surface charge density was 160 ⁇ CZm 2 .
- the luminance ratio of the white particles of the present invention was improved by 7% compared to the luminance ratio of the existing basic white particles. .
- a mixture obtained by kneading 100 parts by weight of the ataryl resin and 20 parts by weight of titanium oxide having an average particle diameter of 200 nm was pulverized and classified to obtain particles having an average particle diameter of 4 to 8 im.
- the luminance factor was 40 ° / 0 .
- the total reflectance of the PMMA sphere having an average particle diameter of 50 / im was 10%.
- existing white materials were coated using Agromaster (Hosokawa Micron Corporation).
- the average particle size was 80 / im, and the surface charge density was 140 ⁇ CZm 2 .
- the luminance factor was 28%.
- Example 4 (powder fluid)
- a hybridizer (Nara Machinery Co., Ltd.) was used for the white particles of Example 1. Then, external additive A (silica H2000Z4, manufactured by Pecker) and external additive B (silica SS20, manufactured by Nippon Silica) were added to these particles, and the mixture was subjected to 500 rpm at 480 rpm. After treatment for a minute, the external additive was immobilized on the surface of the white particles to prepare a white powdery fluid.
- the brightness factor of the white powder fluid of the present invention was improved by 6% compared to the brightness factor of the existing basic white powder fluid.
- a hybridizer manufactured by Nara Machinery Co., Ltd. was used for the white particles of Comparative Example 1, and external additives A (silica H200004, manufactured by Picker) and external additives B ( Silica SS20, manufactured by Nippon Silica Co., Ltd.) was charged, and the mixture was treated at 480 rpm for 5 minutes to immobilize the outer particles on the surface of the white particles to prepare a white powder fluid.
- the luminance factor was 42%.
- Comparative Example 4 (Powder fluid)> The external additive A (silica H2.000Z4, manufactured by Picker) and the external additive ⁇ (silica SS20) were used for the white particles of Comparative Example 2 using a Hypridizer I (manufactured by Nara Machinery Co., Ltd.). And Nippon Silica), and the mixture was treated at 480 rpm for 5 minutes to immobilize the external additive on the surface of the white particles to prepare a white powder fluid. When this was measured in the same manner as in Comparative Example 1, the luminance factor was 28%. '
- An image display panel was manufactured as follows.
- a substrate with electrodes (7 cm ⁇ 7 cm opening) was prepared, and ribs having a height of 400 / m were formed on the substrate to form striped partition walls.
- Lip formation was performed as follows. First paste, an inorganic powder as S io 2, A l 2 0 3, B 2 0 3, B i 2 0 3 and Z n O mixture, melt, cooled, crushed glass powder, heat the resin A curable epoxy resin was prepared, and a paste was prepared with a solvent so as to have a viscosity of 12000 cps. Next, the paste is applied to the entire surface of the prepared substrate, cured by heating at 150 ° C, and the coating and curing are repeated to make the thickness (corresponding to the height of the partition wall) 400 m. It was adjusted.
- a dry photoresist was attached, and a mask was formed by exposure to etching so that a partition pattern having a line of 50 ⁇ ⁇ space 400 im and a pitch of 250 m was formed.
- an extra portion was removed by sandblasting so as to have a predetermined partition shape, thereby forming a desired striped partition.
- cells were formed between the partition walls on the substrate.
- a particle group A As an image display medium, two types of substantially spherical particles having different colors and different charging characteristics are prepared, and a mixture of one of the approximately spherical particles and a third particle having a different charging characteristic in a predetermined amount is referred to as a particle group A.
- a particle group consisting of other substantially spherical particles is referred to as a particle group B.
- the substrate with a rib (opposite substrate) is transferred into a dry container having a humidity of 40% RH or less.
- the particle group A is dispersed into the container as a first particle group from a nozzle provided at an upper portion in the container. Then, the particles A were filled by spraying into cells on a substrate placed at the bottom of the container.
- the particle group B is dispersed as a second particle group into the container from another nozzle provided at the upper part of the container, and is dispersed in the cell on the substrate placed at the lower part of the container (already the particle group A).
- the particle group B was superimposed on the particle group A and filled.
- the filling amount of the particle group A and the particle group B is the same weight, and the volume occupancy of both particle groups combined between the substrates formed by bonding two substrates is 25 V o 1%. It was adjusted.
- the other substrate was superimposed on the substrate filled with particles in the cell, and the periphery of the substrate was bonded with an epoxy-based adhesive, and the particles were encapsulated to produce an image display panel.
- the black to white display was repeated by applying a voltage of 25 O V to the image display device incorporating the manufactured image display panel and inverting the potential.
- the evaluation of the display function was performed using a reflection image densitometer on the contrast ratio at the initial stage, after repeating 100,000 times, repeating 100,000 times, and then standing for 53 times.
- the contrast ratio after repeating 1000 times the initial contrast ratio and after standing for 50 minutes was defined as the retention ratio.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle groups A and B used in Example 1 were prepared as follows.
- Substantially spherical particles composing particle group A are converted to acrylyl urethane resin EAU53B (sub-fine Sub-industry Co., Ltd.) / IPDI-based cross-linking agent Ethacerno, one donor HX (Asia Co., Ltd.), carbon black (MA100: Mitsubishi Chemical Corporation) 4 parts by weight, charge control agent Bontron After adding 2 parts by weight of N07 (manufactured by Orient Chemical Co., Ltd.), kneading, pulverizing with a jet mill, and further applying mechanical impact force using a hybridizer (manufactured by Nara Machinery Co., Ltd.) It was prepared by classifying it after being approximately spherical.
- the substantially spherical particles constituting Particle Group A thus produced were negatively chargeable black particles having an average particle diameter of 9.111 m and a substantially spherical shape and a macroscopically smooth surface.
- silica SS 20 manufactured by Nippon Gilica Co., Ltd. was charged as the third particles, and mixed with a Henschel mixer to prepare Particle Group A.
- the substantially spherical particles constituting the particle group B were prepared by adding 80 parts by weight of tertiary butyl methacrylate monomer and 20 parts by weight of methacrylic acid 2- (getylamino) ethyl monomer to 0.5 part by weight of AIBN (azobisisobutyl mouth-tolyl). ) was dissolved, and 20 parts by weight of oxidized titanium dioxide, which was made lipophilic by dispersing with a coupling agent, was dispersed. The resulting solution was used in an amount of 10 times the amount of 0.5% surfactant (sodium lauryl sulfate).
- AIBN azobisisobutyl mouth-tolyl
- the substantially spherical particles constituting the prepared particle group B are positively-chargeable spherical white particles having an average particle diameter of 8.5 ⁇ and having a macroscopically smooth surface.
- the evaluation results are shown in Table 1 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle groups ⁇ and B used in Example 12 were prepared as follows.
- Substantially spherical particles constituting the particle group A are composed of 0.5 parts by weight of AIBN (azobisisobutyronitrile) in a styrene monomer and a metal-containing azo compound (Bontron S3) as a negatively charged charge control agent. 4: Orient Chemical) 5 parts by weight are dissolved, and 3 parts by weight of carbon black (MA100: Mitsubishi Chemical Corporation) are further separated as a black pigment. The dispersed solution is suspended, polymerized, filtered, and dried in a 10-fold amount of an aqueous solution of 0.5% surfactant (sodium lauryl sulfate), filtered, dried, and then classified (MD S-2: Nippon Pneumatic) Industrial Co., Ltd.).
- AIBN azobisisobutyronitrile
- MA100 Mitsubishi Chemical Corporation
- the substantially spherical particles constituting the prepared particle group A were negatively charged spherical blue particles having an average particle diameter of 8.9 / im and having a macroscopically smooth surface.
- Silica H200004 manufactured by Pokki-Ichisha Co., Ltd. was added as the third particles, and mixed with a Henschel mixer to prepare a particle group A '.
- Substantially spherical particles constituting the particle group B are made of an acrylic polyurethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) / I'PDI cross-linking agent Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.) , 10 parts by weight of titanium oxide, and 2 parts by weight of a charge control agent Pontron E89 (manufactured by Orient Chemical Co., Ltd.), kneaded, pulverized with a jet mill, and a hybridizer (Nara Machinery Co., Ltd.) It was manufactured by applying a mechanical impact force to make it roughly spherical and then classifying it.
- the substantially spherical particles constituting the prepared particle group B are positively chargeable white spherical particles having an average particle diameter of 7.0 Aim and a macroscopically smooth surface.
- Table 1 The evaluation results are shown in Table 1 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle group A and the particle group B used in Comparative Example 11 were prepared as follows.
- the particles constituting the particle group A were converted to acryl urethane resin E AU53 B (manufactured by Asia Kogyo Co., Ltd.) Zl PDI-based cross-linking agent etaserno donor HX (manufactured by Asia Co., Ltd.) and carbon black (MA 10 0: 4 parts by weight of Mitsubishi Chemical Corporation) and 2 parts by weight of the charge control agent Pontrone NO7 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and ground and classified by a jet mill.
- the particles constituting Particle Group A thus produced were black particles having an average particle diameter of 9.3 Aim, irregular shapes, and negatively chargeable black particles having a macroscopically uneven surface.
- silica SS 20 manufactured by Nippon Silica
- Particle Group A The roughly spherical particles constituting the particle group B were added to 180 parts by weight of t-butyl methacrylate monomer and 20 parts by weight of methacrylic acid 2- (getylamino) ethyl monomer, and 0.5 parts by weight of AIBN (azo Bisisoptyronitrile) was dissolved and treated with a coupling agent to disperse 20 parts by weight of titanium oxide, which was made lipophilic. The resulting solution was diluted 10 times with a 0.5% surfactant (laurinole).
- AIBN azo Bisisoptyronitrile
- the substantially spherical particles constituting the prepared particle group B are positively-chargeable spherical white particles having an average particle diameter of 8.5 IX m and having a macroscopically smooth surface.
- the evaluation results are shown in Table 1 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle group A and the particle group B used in Comparative Example 12 were prepared as follows.
- the roughly spherical particles constituting the particle group A are composed of 0.5 parts by weight of AIBN (azobisisobutyronitrile) in a styrene monomer and a metal-containing azo compound (Pontrone S34: Orient) as a negatively charged charge control agent.
- AIBN azobisisobutyronitrile
- Pontrone S34 Orient
- Chemical 5 parts by weight are dissolved, and as a black pigment, carpump rack (MA100: Mitsubishi Chemical) 3 parts by weight is dispersed in a 10-fold amount of 0.5% surfactant ( After suspension, polymerization, filtration and drying in an aqueous solution of sodium lauryl sulfate, the mixture was prepared using a classifier (MD S-2: Nippon Pneumatic).
- the substantially spherical particles constituting the prepared particle group A were negatively chargeable spherical black particles having an average particle diameter of 8.9 ⁇ and a macroscopically smooth surface.
- silica 20000 manufactured by Pecker Co., Ltd. was added as third particles, and mixed with a Henschel mixer to prepare a particle group.
- the particles constituting the particle group B are acrylacrylic resin E AU53 B (manufactured by Asia Kogyo Co., Ltd.) Zl PDI-based cross-linking agent Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.) and 10 parts by weight of titanium oxide , Charge control agent Bontron E89 (Orient Chemical Co., Ltd. 2 parts by weight) were added, kneaded, and pulverized and classified by a jet mill.
- the particles constituting the prepared particle group B are white particles having an average particle diameter of 7.0 ⁇ m, irregular shapes, macroscopically uneven surfaces, and positively chargeable white particles. The evaluation results are shown in Table 1 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle group A and the particle group B used in Comparative Example 13 were prepared as follows.
- the substantially spherical particles constituting the particle group A were converted to acrylonitrile resin E AU53B (manufactured by Asia Kogyo Co., Ltd.) / IPDI cross-linking agent Ethacell Nodner HX (manufactured by Asia Kogyo Co., Ltd.) using carbon black ( MA100: Mitsubishi Chemical Corporation) 4 parts by weight, 2 parts by weight of Pontron NO 7 charge control agent (manufactured by Orient Chemical Co., Ltd.), kneading, pulverization by jet mill, and hybridizer Using a device (manufactured by Nara Machinery Co., Ltd.), a mechanical impact force was applied to form a roughly spherical shape, followed by classification.
- the substantially spherical particles constituting the prepared particle group A are negatively chargeable black particles having an average particle diameter of 9.1 ⁇ m, a substantially spherical shape, and a macroscopically smooth surface.
- the roughly spherical particles constituting the particle group B were prepared by adding 180 parts by weight of tertiary butyl methacrylate monomer and 20 parts by weight of methacrylic acid 2- (getylamino) ethyl monomer to 0.5 parts by weight of AIBN (azobisisobutyronitrile). ) Is dissolved, and 20 parts by weight of titanium oxide which is made lipophilic by treatment with a coupling agent is dispersed, and 10 times the amount of a 0.5% aqueous solution of a surfactant (sodium lauryl sulfate) is added. After suspending, polymerizing, filtering and drying, it was prepared using a classifier (MDS-2: Japan-Umatic Co., Ltd.). The substantially spherical particles constituting the prepared particle group B are positively charged spherical white particles having an average particle diameter of 8.5 ⁇ and having a macroscopically smooth surface. The evaluation results are shown in Table 1 below.
- the agglomeration of the panel was evaluated in which white particles with low dielectric constant and black particles with different dielectric constants were both enclosed as an image display medium.
- particles constituting the image display medium were prepared as follows. Varying the amount of carbon black added to the styrene-acrylic resin, as shown in Table 2 below Black particles having different dielectric constants as in Test Nos. 1 to 3 of the Examples and Comparative Example Tests Nos. 4 and 5 were produced.
- the particles were sealed between the substrate electrodes as follows.
- the fabricated black particles with different dielectric constants were each enclosed in a panel together with white particles with low dielectric constant, and the tests of Examples No. 1 to 3 and Comparative Example Tests No. 4 and 5 where only the dielectric constant of the black particles was different Was prepared.
- the evaluation was performed as follows. First, at the stage of preparing the particles, the dielectric constant of the particles was measured. The dielectric constant of the whole particles was measured by processing the particles into a sheet and measuring the capacitance of a parallel plate capacitor using this as a dielectric material. The dielectric constant was calculated from the measured value, the distance between the electrodes, and the area of the electrode, and this was defined as the dielectric constant of the particles. The measurement was performed using the following: ⁇ Impedance gain of Packard Co., Ltd. ⁇ Phase analyzer: HP4194A and electrode for dielectric measurement of the peripheral equipment of the same device: HP 16451B. Here, the measured values at a frequency of 100 Hz are described.
- the test panel was evaluated by applying an AC voltage of 1 Hz and 200 V between the two substrate electrodes of the test panel, and causing the internal particles to reciprocate between the electrode plates many times at the same frequency as the applied voltage. .
- the process of reciprocating the particles was observed, and the time during which the particles agglomerated and could not be moved by voltage application was measured.
- the test lasted up to 10,000 seconds. Particles that did not agglomerate until the end of the test were regarded as good products (denoted as ⁇ in Table 1 below), and particles that agglomerated in the middle were deemed defective (denoted as X in Table 2 below).
- the aggregation of the particles was visually determined. The results are shown in Table 2 below.
- the particles constituting the image display medium should be composed of a low dielectric constant insulating material having a low relative dielectric constant, and preferably, the image display medium is composed of It can be seen that the relative permittivity of the resulting particles is preferably 5.0 or less.
- the reflectance (hiding power) of the obtained white particles was measured.
- the reflectance was determined by scattering white particles on a glass substrate and measuring the reflectance per layer measured by a Macbeth densitometer. The measurement result was 57%.
- the reflectance of the obtained white particles was measured in the same manner as in Example 31, the reflectance was 18%.
- Titanium oxide (CR-50, manufactured by Ishihara Sangyo Co., Ltd.) 100 parts by weight and 100 parts by weight of acrylic resin are kneaded with a twin-screw kneader, pulverized and classified, and the volume of titanium oxide White particles having a fraction of 23% and an average particle diameter of 9 m were obtained.
- the reflectance of the obtained white particles was measured in the same manner as in Example 31. As a result, the reflectance was 38%.
- the image display panels of the examples and comparative examples were prepared by the following method and evaluated according to the following criteria.
- An image display panel was manufactured as follows.
- the ribs were formed as follows. First paste, a mixture of S io 2, A l 2 0 3, B 2 0 3, B i 2 0 3 and Z N_ ⁇ as inorganic powder, melting, cooling, and pulverized glass powder, heat the resin A curable epoxy resin was prepared, and a paste was prepared with a solvent so as to have a viscosity of 12000 cps. Next, the paste is applied to the entire surface of the prepared substrate and cured by heating at 150 ° C. By adjusting the thickness, the thickness (corresponding to the height of the partition) was adjusted to 400/1 m.
- a dry photoresist was attached, and a mask was formed by exposure to etching so that a partition pattern of 50 ⁇ m in line, 400 ⁇ m in space, and 250 / im pitch was formed.
- an extra portion was removed by sandblasting so as to have a predetermined partition shape, thereby forming a desired striped partition.
- cells were formed between the partition walls on the substrate.
- particle group A is set as the first particle group, dispersed from the nozzle provided at the upper part of the container into the container, and dispersed in the cells on the substrate placed at the lower part of the container.
- Group A was filled.
- the particle group B is dispersed as a second particle group into the container from another nozzle provided at the upper portion of the container, and is dispersed in the cell on the substrate placed at the lower portion of the container (particle group A is already filled).
- the particle group B was filled over the particle group A by spraying.
- the filling amount of the particle group A and the particle group B was set to the same weight, and the volume occupancy ratio of both particle groups to the substrate formed by laminating the two substrates was 26 V o 1% (No. (1 invention) or 28 Vo 1% (second invention).
- the other substrate was superimposed on the substrate filled with particles in the cell, and the periphery of the substrate was bonded with an epoxy-based adhesive, and the particles were encapsulated to produce an image display panel.
- the black to white display was repeated by applying a voltage of 25 OV to the image display device incorporating the manufactured image display panel and inverting the potential. Evaluation of the display function was performed using a reflection image densitometer on the contrast ratio of the panel at the initial stage, after repeating 1000 times, after repeating 1000 times, and after standing for 5 days.
- the contrast ratio after repeating 1000 times the initial contrast ratio and after standing for 5 days was defined as the retention ratio.
- An image display panel was manufactured according to the above-described image display panel manufacturing method, and the above-described display functions were evaluated.
- the particle group A and the particle group B used in Example 41 were prepared as follows.
- Particle group A is composed of an acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) / 1 PDI-based cross-linking agent Ethacell Nodner HX (manufactured by Asia Kogyo Co., Ltd.) and a carbon black (MA100: Mitsubishi). 4 parts by weight (manufactured by Kagaku Co., Ltd.) and 2 parts by weight of the charge control agent Bontron NO7 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and pulverized and classified with a jet mill.
- the prepared particle group A was a negatively chargeable black particle group having an average particle diameter of 9.1 ⁇ and having macroscopic irregularities on the surface.
- Particle group I was prepared by dissolving 0.5 parts by weight of AIBN (azobisisobutyronitrile) in 80 parts by weight of tertiary butyl methacrylate monomer and 20 parts by weight of methacryloleic acid 2- (getinoleamino) ethyl monomer.
- AIBN azobisisobutyronitrile
- the liquid obtained by dispersing 20 parts by weight of lipophilic titanium oxide by treating with a coupling agent is suspended in 10 times the amount of a 0.5% aqueous solution of a surfactant (sodium lauryl sulfate) and polymerized. After being filtered and dried, it was prepared using a classifier (MDS-2: manufactured by Japan-Umatic Co., Ltd.).
- the prepared particle group B was positively chargeable spherical white particles having an average particle diameter of 8. and having no macroscopic unevenness on the surface.
- the evaluation results are shown in Table 4 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle groups A and B used in Example 42 were prepared as follows.
- Particle group A is composed of 0.5 parts by weight of AIBN (azobisisobutyronitrile) in a styrene monomer and a gold-containing azo compound (Bontron S) as a negative charge control agent.
- AIBN azobisisobutyronitrile
- Bontron S gold-containing azo compound
- the prepared particle group A was a negatively chargeable spherical black particle group having an average particle diameter of S. 9 ⁇ and having no macroscopic unevenness on the surface.
- Particle group ⁇ is composed of acrylic urethane resin EAU53 ⁇ (manufactured by Asia Industries) / ⁇ PD I-based cross-linking agent Ethacell Hardnat IX (manufactured by Asia Industries), 10 parts by weight of titanium oxide, and charge control 2 parts by weight of agent Bontron ⁇ 89 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and then pulverized and classified by a jet mill.
- the prepared particle group I was a positively charged white particle group having an average particle diameter of 7.0 / m and having macroscopic irregularities on the surface.
- the evaluation results are shown in Table 4 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle group A and the particle group B used in Example 43 were prepared as follows.
- Particle group A is composed of styrene monomer, azo compound (5 parts by weight), charge control agent Bontron NO7 (manufactured by Orient Chemical Co., Ltd., 5 parts by weight), initiator AIBN (0.5 parts by weight)
- the particle diameter was adjusted by a classifier.
- a hybridizer manufactured by Nara Machinery Co., Ltd.
- fine-particle silica H2050, manufactured by Picker
- fine-particle silica SS20, manufactured by Nippon Silica
- Particle group ⁇ is composed of 80 parts by weight of methinoremethacrylate monomer and 20 parts by weight of methacrylic acid 2- (ethylenamino) ethyl monomer, and 0.5 part by weight of ⁇ ⁇ ⁇ (azo Dissolve 20 parts by weight of lipophilic titanium oxide by dissolving bisisobutyl mouth-tolyl) and treating with a coupling agent. Dissolve 10 times the amount of 0.5% surfactant (sodium lauryl sulfate) After suspending in a zk solution, polymerizing, filtering and drying, it was prepared using a pulverizer and classifier (FM-120: manufactured by Nippon Pneumatic Industries, Ltd.). The prepared Particle Group B was positively chargeable spherical white particles having an average particle diameter of 7. and having no macroscopic unevenness on the surface. The evaluation results are shown in Table 4 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle groups A and B used in Comparative Example 41 were prepared as follows.
- Particle group A is composed of acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) ZIPDI-based cross-linking agent Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.), car pump rack (MA100: Mitsubishi Chemical Corporation) Co., Ltd.) 4 parts by weight and 2 parts by weight of the charge control agent Bontron NO7 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and ground and classified by a jet mill.
- the prepared particle group A was a negatively chargeable black particle group having an average particle diameter of 9. l ⁇ in and having macroscopic irregularities on the surface.
- Particle group B is composed of acrylic urethane resin E AU53B (manufactured by Asia Kogyo Co., Ltd.) ZIPDI-based cross-linking agent Ethaserno donor HX (manufactured by Asia Kogyo Co., Ltd.), 10 parts by weight of titanium oxide, and Bontron charge control agent 2 parts by weight of E89 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and then pulverized and classified by a jet mill to produce a mixture.
- the prepared particle group B was a group of positively chargeable white particles having an average particle diameter of 7. Om and having macroscopic irregularities on the surface. The evaluation results are shown in Table 4 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle group A and the particle group B used in Comparative Example 42 were prepared as follows.
- Particle group A is composed of 0.5 parts by weight of AIBN (azobisisobutyl-tolyl) in a styrene monomer and a metal-containing azo-based compound (Bontron S34: manufactured by Orient Chemical Co., Ltd.) as a negative charge controller.
- the prepared particle group A was negatively chargeable spherical black particles having an average particle diameter of 8.9 / zm and having no macroscopic unevenness on the surface.
- Particle group B is composed of 80 parts by weight of tertiary butyl methacrylate monomer and 20 parts by weight of methacrylic acid 2- (getylamino) ethyl monomer, and 0.5 part by weight of A
- a solution obtained by dissolving IBN (azobisisopuchi mouth-tolyl), dispersing 20 parts by weight of lipophilic titanium oxide by treating with a force coupling agent, and dispersing 10 times the amount of 0.5% surfactant After suspension in an aqueous solution of sodium lauryl sulfate), polymerization, filtration, and drying, it was prepared using a classifier (MDS-2: manufactured by Nippon Yuematic Industrial Co., Ltd.).
- the prepared particle group B was positively chargeable spherical white particles having an average particle diameter of 8.5 / m and no macroscopic irregularities on the surface.
- the evaluation results are shown in Table 4 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle group A and the particle group B used in Example 51 were prepared as follows.
- Particle group A is a mixture of acrylic urethane resin 'Eat EAU53B (manufactured by Asia Kogyo Co., Ltd.) / 1 Add 4 parts by weight of a rack (MA I 00: manufactured by Mitsubishi Chemical Corporation) and 2 parts by weight of the charge control agent Bontron NO7 (manufactured by Orient Chemical Co., Ltd.), knead the mixture, pulverize and classify it with a jet mill. Produced.
- the prepared particle group A was a negatively chargeable black particle group having an average particle diameter of 9.1 ⁇ m and having macroscopic irregularities on the surface.
- Particle group B was prepared by dissolving 0.5 parts by weight of AIBN (azobisisobutyl mouth-tolyl) in 80 parts by weight of tertiary butyl methacrylate monomer and 20 parts by weight of methacrylic acid 2_ (getylamino) ethyl monomer, and treated with a coupling agent.
- AIBN azobisisobutyl mouth-tolyl
- methacrylic acid 2_ getylamino
- the liquid obtained by dispersing 20 parts by weight of lipophilic titanium oxide is suspended and polymerized in 10 volumes of a 0.5% aqueous solution of a surfactant (sodium lauryl sulfate), filtered, and dried.
- a surfactant sodium lauryl sulfate
- the average particle diameter is 8.5 / m and the surface is positively charged, spherical white without macroscopic unevenness.
- a group of particles was prepared, and then, using a Henschel mixer, silica particles (H2050, manufactured by PEKKA Co., Ltd.) of negative chargeability were added to the spherical white particle group, and these particles were mixed. Electrostatically adheres to the surface of spherical white particles To produce a particle group B was.
- the prepared particle group B was a group of positively chargeable white particles having fine particles adhered to the particle surface without macroscopic irregularities on the surface.
- the evaluation results are shown in Table 5 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display functions described above were evaluated.
- the particle group A and the particle group B used in Example 52 were prepared as follows.
- the particle group A is composed of 0.5 parts by weight of AIBN (azobisisobutyl mouth ethryl) and 5 parts by weight of a metal-containing azo compound (Bontron S34: manufactured by Orient Chemical Co., Ltd.) as a negative charge control agent in a styrene monomer. And 3 parts by weight of carbon black (MA100: manufactured by Mitsubishi Chemical Corporation) as a black pigment were dispersed in a 10-fold amount of 0.5% surfactant (sodium laurinole sulfate). After suspending in a 7j solution, polymerizing, filtering and drying, a classifier (MD S-2: Nippon New- First, a group of negatively-conductive spherical black particles having an average particle size of 8.
- AIBN azobisisobutyl mouth ethryl
- a metal-containing azo compound (Bontron S34: manufactured by Orient Chemical Co., Ltd.) as a negative charge control agent in a styrene monomer.
- Particles A were prepared by adding positively charged fine particles of titanium oxide to the particles and mixing and electrostatically adhering these particles to the surface of the spherical black particles.
- the prepared particle group A was a group of negatively-chargeable black particles having fine particles adhered to the particle surface without macroscopic irregularities on the surface.
- Particle group B consists of acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) / 1 PD I-based cross-linking agent Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.), 10 parts by weight of titanium oxide, and Bontron E89 (charge control agent). Orient Chemical Co., Ltd.) (2 parts by weight) was added, kneaded, and then pulverized and classified by a jet mill to produce a mixture.
- the prepared particle group B was a group of positively chargeable white particles having an average particle diameter of 7. ⁇ and having macroscopic irregularities on the surface. The evaluation results are shown in Table 5 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display functions described above were evaluated.
- the particle group I and the particle group B used in Comparative Example 51 were prepared as follows.
- Particle group A is composed of acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) / 1 PD I-type cross-linking agent Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.) and car pump rack (MA 100: Mitsubishi Chemical Corporation) 4 parts by weight and 2 parts by weight of a charge control agent Bontron N07 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and then pulverized and classified by a jet mill to prepare a mixture.
- the prepared particle group A was a negatively-chargeable black particle group having an average particle diameter of 9 ⁇ m and having macroscopic irregularities on the surface.
- Particle group B is composed of acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) ZI PD I-based cross-linking agent Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.), 10 parts by weight of titanium oxide, and charge control agent Bontron E 89 ( Orient Chemical Co., Ltd.) (2 parts by weight) was added, kneaded, and then pulverized and classified by a jet mill to produce a mixture. Fabricated particles Group B was a group of positively chargeable white particles having an average particle diameter of 7. Om and having macroscopic irregularities on the surface. The evaluation results are shown in Table 5 below.
- An image display panel was manufactured according to the above-described method for manufacturing an image display panel, and the display function described above was evaluated.
- the particle group A and the particle group B used in Comparative Example 52 were prepared as follows. '
- Particle group A is composed of 0.5 parts by weight of AIBN (styrene) and 5 parts by weight of a metal-containing azo-based compound (Bontron S34: manufactured by Orient Chemical Co., Ltd.) as a charge control agent for negative charges. And 3 parts by weight of carbon black (MA100: manufactured by Mitsubishi Chemical Corporation) as a black pigment were dispersed in a 10-fold amount of 0.5% surfactant (sodium lauryl sulfate). After suspending in an aqueous solution, polymerizing, filtering, and drying, it was prepared using a classifier (MDS-2: manufactured by Japan-Umatic Co., Ltd.). The prepared particle group A was negatively chargeable spherical black particles having an average particle diameter of 8.9 ⁇ and no macroscopic irregularities on the surface.
- AIBN styrene
- a metal-containing azo-based compound Bontron S34: manufactured by Orient Chemical Co., Ltd.
- surfactant sodium lauryl sulfate
- Particle group ⁇ dissolves 0.5 parts by weight of AIBN (azobisisobutyl mouth-tolyl) in 80 parts by weight of tertiary butyl methacrylate monomer and 20 parts by weight of methacrylic acid 2- (getinoleamino) ethyl monomer, and provides a coupling agent.
- a liquid obtained by dispersing 20 parts by weight of the lipophilic titanium oxide by treatment is suspended and polymerized in 10 times the amount of a 0.5% aqueous solution of a surfactant (sodium lauryl sulfate), followed by filtration. After drying, it was prepared using a classifier (MD S-2: manufactured by Japan-Umatic Co., Ltd.).
- the produced particle group B was a positively charged spherical white particle having an average particle diameter of 8.5 ⁇ and having no macroscopic unevenness on the surface.
- Table 5 The evaluation results are shown in Table 5 below. Table 5
- one particle was a particle with macroscopic irregularities on the surface, and the other particle was a particle without macroscopic irregularities on the surface and particles were electrostatically attached to the surface.
- Comparative Example 51 in which no fine particles to be electrostatically attached were used, and all the particles were macroscopically uneven, and none of the particles had macroscopic unevenness. It can be seen that, at any point in time, the contrast ratio was higher than that of Comparative Example 52 in which the particles were used. It can be seen that the image display panel according to the second embodiment of the fifth invention of the present invention has excellent durability even in repeated use.
- Example 6 1 (white particles)>
- titanium oxide as a white pigment Ishihara 100 parts by weight, 200 parts by weight or 300 parts by weight of Taipeta CR95 (manufactured by Sangyo Co., Ltd.) and hollow particles: SX866 (A) ( ⁇ 0. 3 ⁇ (primary particles), inner diameter 0.2 ⁇ Cross-linked styrene-acrylic acid 10 to 60 parts by weight, other CCA and various fillers (in each case, the same amount) are added, kneaded, and then jet-milled.
- PMMA Delpet 8 ONH, specific gravity 1.19, manufactured by Asahi Kasei Corp.
- the white reflectance (whiteness) of the obtained white particles of the present invention and comparative examples was measured.
- the white reflectance was measured from the outside of the glass plate with a transparent electrode body made of 1.1 mm thick ITO, with the particles being evenly spread on the substrate glass surface. It was calculated as a rate.
- the volume filling rate was determined as ⁇ (volume of titanium oxide + volume of hollow particles) / (volume of whole particles (resin + titanium oxide + hollow particles)) ⁇ X100. The results are shown in Table 6 below.
- Example No. 3 of the present invention in Example 1 200 parts by weight of titanium oxide, 30 parts by weight of hollow particles
- An external additive A sica ⁇ [2000 4, manufactured by Picker
- an external additive B sica SS20, manufactured by Nippon Silica
- the whiteness of the obtained white powder of the present invention was measured in the same manner as in Example 61. As a result, the whiteness showed a good value of 45% or more.
- thermosetting resin Polyester resin (for PCM powder coating) + block isocyanate-based upica coat GV-570 (manufactured by Nippon Upika Co., Ltd.), cross-linking agent: Vestagon B1530 (manufactured by Degussa), and , Curing catalyst: Neostan U-100 (manufactured by Nitto Kasei Co., Ltd.), titanium oxide: Taipeta CR-95 (manufactured by Ishihara Sangyo Co., Ltd.), CCA: Bontron E-84 (manufactured by Orient Chemical Co., Ltd.) The mixture was kneaded with a twin-screw kneader to obtain a compound.
- the kneading temperature was 120 ° C.
- the obtained compound was 200.
- CX was hot pressed for 10 minutes, and the thermosetting resin as the base resin was crosslinked and cured by heating. Then, it was pulverized by a jet mill to obtain particles of Examples Nos. 1 to 4 of the present invention.
- Example Test Nos. 1 to 4 A curing reaction was carried out on the obtained particles of Example Test Nos. 1 to 4 and the particles of Comparative Example Test No. 1 using a sheet monoredo of 15 OmmX15 OmmX2.5 mm. Thereafter, the temperature was gradually increased, and the temperature at which the deformation of the particles started and the temperature at which the particles began to fuse to the glass substrate were measured. The results are shown in Table 7 below.
- Example Test Nos. 1 to 4 of the present invention in which the thermosetting resin was cured by heat crosslinking were compared with the particles of Comparative Example Test No. 1 using the thermoplastic resin. It can be seen that the heat resistance was greatly improved without deformation and fusion to high temperatures.
- a substrate with electrodes (7 cmX 7 cmD) was prepared, and ribs having a height of 400 ⁇ were formed on the substrate to form striped partition walls.
- the formation of the lip proceeded as follows. First paste, S i o 2 as the inorganic powder, A 1 2 0 3, the ⁇ 2 0 3, B i 2 0 3 and ⁇ mixtures Ita_ ⁇ , melting, cooling, and pulverized glass powder, the resin A thermosetting epoxy resin was prepared, and a paste was prepared with a solvent so as to have a viscosity of 12000 cps. Next, the paste was applied on the prepared substrate, cured by heating at 150 ° C, and this coating and curing were repeated to adjust the thickness (corresponding to the height of the partition) to 400 / m. .
- a dry photoresist was used, and a mask was formed by exposure to etching to form a partition pattern of 50 ⁇ m in line, 400 ⁇ m in space, and 250 ⁇ m in pitch.
- an extra portion was removed by sand blasting so as to have a predetermined partition shape, thereby forming a desired striped partition.
- the particle group A is dispersed as a first particle group into the container from the nozzle provided at the upper part of the container, and is dispersed in the cells on the substrate placed at the lower part of the container. Thus, the particle group A was filled.
- the particle group B is dispersed as a second particle group into the container from another nozzle provided at the upper part of the container, and is dispersed in the cell on the substrate placed at the lower part of the container (particularly, the particle group A To the particle group A by spraying.
- the filling amount of the particle group A and the particle group B was set equal to each other by weight, and the volume occupancy of both particle groups combined between the substrates that can be bonded by two substrates was 26 V o 1%. It was adjusted.
- the other substrate was superimposed on the substrate filled with particles in the cell, and the periphery of the substrate was bonded with an epoxy-based adhesive, and the particles were encapsulated to produce an image display panel.
- the black to white display was repeated by applying a voltage of 25 O V to the image display device incorporating the manufactured image display panel and inverting the potential.
- the evaluation of the display function is performed for the contrast ratio and the reflection density at the time of displaying white, and the initial, after repeating 1000 times, and after repeating 1000 times, respectively, using a reflection image densitometer. It was measured.
- the contrast ratio is defined as a contrast ratio: reflection density in black display / reflection density in white display.
- Particle groups (particle group A and particle group B) were prepared as two types of image display media.
- Particle group A is composed of acrylic urethane, EAU53 B (manufactured by Asia Kogyo Co., Ltd.), ZI PD I-based citrus agent Ethacellhard, "I HX (manufactured by Asia Kogyo Co., Ltd.), carbon black (MA100: Mitsubishi Chemical Corporation) Co., Ltd.) 4 parts by weight, 2 parts by weight of the charge control agent Pontron NO 7 (manufactured by Orient Chemical Co., Ltd.), knead the mixture, pulverize with a jet mill, and make the primary particles 140 ° by hot pressing.
- Particle group A is composed of acrylic urethane, EAU53 B (manufactured by Asia Kogyo Co., Ltd.), ZI PD I-based citrus agent Ethacellhard, "I HX (manufactured by Asia Kogyo Co., Ltd.), carbon black (MA
- the sheet was sheeted with C to obtain a sheet having a thickness of 8 ⁇ , which was heated and stretched by a stretching machine to obtain a sheet having a thickness of 8 ⁇ .
- the surface of the crushed pieces was slightly melted at a hot-air temperature of 450 ° C to obtain flat round particles.
- the produced particle group A was negatively charged, Flat round shape with an average particle size of 9.4 ⁇ It was the color particle groups.
- Particle group ⁇ is composed of acrylic urethane resin EAU53 ⁇ (manufactured by Asia Kogyo Co., Ltd.) / ⁇ PD I cross-linking agent Ethacell Hardener ⁇ (manufactured by Asia Kogyo Co., Ltd.), 10 parts by weight of titanium oxide, and Bontron charge control agent ⁇ 89 2 parts by weight (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and then produced in the same manner as in the procedure for producing the particle group.
- the prepared particle group B was a positively charged green raw particle group having a flat round shape and a white particle having an average particle diameter of 9. ⁇ .
- the display function was evaluated using an image display device incorporating an image display panel made of these particle groups. Table 8 shows the results.
- Particle group ⁇ is composed of acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) / 1 PD I-type crosslinker Ethacell Hardener HX (manufactured by Asia Co., Ltd.) and carbon black (MA100: manufactured by Mitsubishi Chemical Corporation) 4 parts by weight and 2 parts by weight of a charge control agent Bontron NO7 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and then pulverized and classified by a jet mill to prepare a mixture.
- the prepared particle group A was a black particle group having negative chargeability and an average particle diameter of 9.0 ⁇ m.
- For the particle group B a flat white particle group having a positive chargeability and an average particle diameter of 9, ⁇ ⁇ ⁇ , which was produced in Example 81, was used.
- the display function was evaluated using an image display device incorporating an image display panel made of these particle groups. Table 8 shows the results.
- Particle group ⁇ is a negatively-charged, average particle diameter of 9.4 nm (a black particle group having a D flat round shape) prepared in Example 81.
- Particle group B is a tertiary butyl methacrylate monomer 80.
- the display function was evaluated using an image display device incorporating an image display panel made of these particle groups. Table 8 shows the results.
- particle group A 0.5 parts by weight of AIBN (azobisisobutyroletrenole) and 5 parts by weight of a metal-containing azo-based compound (Bontron S34: Orient Chemical Co., Ltd.) as a negatively charged charge control agent were added to the styrene monomer. Dissolve and further disperse 3 parts by weight of carbon black (MA100: manufactured by Mitsubishi Chemical Corporation) as a black pigment, suspend 10 times the volume of 0.5% surfactant (sodium lauryl sulfate) 7_R solution. After turbidity, polymerization, filtration and drying, a classifier (MDS-2: Nippon Pneumatic)
- the prepared particle group A has an average particle size of 8.
- Particle group B is composed of 80 parts by weight of tertiary butyl methacrylate monomer and 0.5 parts by weight of AIBN (azobisisobutyronitrile) was dissolved in 20 parts by weight of lylic acid 2- (getylamino) ethyl monomer, and 20 parts by weight of lipophilic titanium oxide was treated with a coupling agent.
- AIBN azobisisobutyronitrile
- the liquid obtained by dispersion is suspended in 10 times the volume of a 0.5% aqueous solution of a surfactant (sodium lauryl sulfate), polymerized, filtered, and dried, and then classified into a classifier (MDS-2: A group of spherical white particles having a positive chargeability and an average particle diameter of 8.5 xm, which was produced using Nippon Yumatic Industrial Co., Ltd.).
- a surfactant sodium lauryl sulfate
- the display function was evaluated using an image display device incorporating an image display panel made of these particle groups. Table 8 shows the results.
- Example 81 and Example 82 in which the particle group A (white) had a flat round shape, the white reflection density was high even at the initial stage, and the white reflection density was reduced even after repeated inversion display. It was found that the decrease in contrast and contrast ⁇ were both small. Further, in Example 83, in which the particle group B (black) was a flat round shape, the initial white reflection density was lower than that in Example 81, Example 82, in which the particle group A (white) was a flat round shape. However, it was found that the decrease in the white reflection density and the decrease in the contrast ratio were small even after repeated inversion display.
- a substrate with electrodes (7 cm ⁇ 7 cm opening) was prepared, and ribs having a height of 400 / m were formed on the substrate to form striped partition walls.
- the ribs were formed as follows. First paste, a mixture of S io 2, A 1 2 0 3 as the inorganic powder, B 2 0 3, B i 2 0 3 and Z nO, melting, cooling, and pulverized glass powder, hot hardness as resin An epoxy resin having a dagger property was prepared, and a paste was prepared with a solvent so as to have a viscosity of 12000 cps. Next, the paste was applied on the prepared substrate, heated and cured at 150 ° C., and the application and curing were repeated to adjust the thickness (corresponding to the height of the partition) to 400 ⁇ .
- a dry photoresist was attached, and a mask was formed by exposure to etching so that a partition pattern having a line of 50 m, a space of 400 / im, and a pitch of 250 ⁇ m was formed.
- an extra portion was removed by sandblasting so as to have a predetermined partition shape, thereby forming a desired striped partition.
- particle group A and particle group B Prepare two types of image display media (particle group A and particle group B) with different colors and charging characteristics, and transfer the substrate with ribs (counter substrate) into a dry container with a humidity of 40% RH or less.
- the particle group A was filled by dispersing the particle group A as a first particle group from a nozzle provided in the upper part of the container into a cell on a substrate placed at the lower part of the container. .
- the particle group B was set as a second particle group, and another nozzle provided at the upper part in the container was used. Then, the particles were dispersed into the container and sprayed into the cells on the substrate placed at the bottom of the container (particle group A was already filled), so that particles were overlaid on particle group A.
- the filling amount of the particle group A and the particle group B is set to be the same weight, and the volume occupancy of both particle groups combined between the substrates that can be bonded by two substrates is 25 V o 1%. It was adjusted. ⁇
- the other substrate was superimposed on the substrate filled with particles in the cell, and the periphery of the substrate was bonded with an epoxy-based adhesive, and the particles were encapsulated to produce an image display panel.
- the black to white display was repeated by applying a voltage of 25 O V to the image display device incorporating the manufactured image display panel and inverting the potential.
- the evaluation of the display function is performed for the contrast ratio and the reflection density at the time of displaying white, and the initial, after repeating 1000 times, and after repeating 1000 times, respectively, using a reflection image densitometer. It was measured.
- Particle groups (particle group A and particle group B) were prepared as two types of image display media.
- Particle group A is composed of acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) ZIPDI crosslinker Exelnodnor HX (manufactured by Asia Kogyo Co., Ltd.) and carbon black (MA100: Mitsubishi Chemical Co., Ltd.) 4 parts by weight) and 2 parts by weight of the charge control agent Bontron NO7 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and pulverized and classified by a jet mill.
- the prepared particle group A was a negatively chargeable black particle group having an average particle diameter of 8.1 ⁇ m. Furthermore, when a part of the sample was sampled and observed under a microscope, particles having a particle size exceeding 10 ⁇ m were observed.
- Particle group B was obtained by adding acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) / ⁇ PDI crosslinker Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.) to titanium dioxide 10 parts by weight and 2 parts by weight of a charge control agent Bontron E 89 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and then pulverized and classified by a jet mill.
- the produced particle group B was a positively chargeable white particle group having an average particle diameter of 9.7 ⁇ . Further, when a part of the sample was sampled and observed under a microscope, particles having a particle size of less than 8 xm were observed. '
- the display function was evaluated using an image display device incorporating an image display panel using these particles as an image display medium. Table 9 shows the results.
- Particle group A is composed of acrylic urethane resin EAU53 B (manufactured by Asia Kogyo Co., Ltd.) Zl PD I-based cross-linking agent Ethacel Nodner HX (manufactured by Asia Co., Ltd.) and carbon black (MA100: manufactured by Mitsubishi Chemical Corporation) ) 4 parts by weight, 2 parts by weight of the charge control agent Pontron NO 7 (manufactured by Orient Chemical Co., Ltd.) are added, kneaded, pulverized and classified by a jet mill, and further classified into a classifier (MDS-2: Yomoto-U). Particles having a particle size of 10 zm or more were classified by over-force classification using Matic Industrial Co., Ltd.).
- the prepared particle group A was a black particle group having a negative chargeability and an average particle diameter of 7.4 m. Further, when a part of the sample was sampled and observed under a microscope, particles having a particle size exceeding ⁇ ⁇ were not observed.
- Particle group ⁇ is composed of acrylic urethane resin EAU53 ⁇ (manufactured by Asia Kogyo Co., Ltd.) / 1 PD I-based cross-linking agent Ethacernodonor ⁇ (manufactured by Asia Co., Ltd.), 10 parts by weight of titanium dioxide, and pontron, a charge control agent No. 89 (manufactured by Orient Chemical Co., Ltd.) 2 parts by weight are added, kneaded, and then pulverized and classified by a jet mill, and then a classifier having a particle diameter of 8 ⁇ m or less (MDS-2: Japan-Umatic The product was produced by undercut classification using Kogyo Co., Ltd.).
- the prepared particle group B was a positively chargeable white particle group having an average particle diameter of 9.8 m. Further, when a part of the sample was sampled and observed under a microscope, particles having a particle size of less than 8 xm were not observed. An image display panel manufactured using these particles as an image display medium was incorporated. The display function was evaluated using an image display device. Table 9 shows the results.
- the particle group A a black particle group having an average particle diameter of 7.4 ⁇ m, obtained by classifying the negatively chargeable particles having a particle diameter of 10 m or more and produced in Example 92, was used.
- Particle group B is composed of 80 parts by weight of tertiary butyl methacrylate monomer and 20 parts by weight of methacrylic acid 2- (getylamino) ethyl monomer, and 0.5 part by weight of A
- Dissolve BN (azobis isopuchi mouth-tolyl), disperse 20 parts by weight of lipophilic titanium dioxide by treating with a coupling agent, and add 10 times the amount of 0.5% surfactant (lauryl) (Sodium sulfate)
- a classifier MDS-2: manufactured by S-Pneumatic Industrial Co., Ltd.
- the prepared particle group B was a group of positively chargeable spherical white particles having an average particle diameter of 9.6 m. Further, when a part was sampled and observed under a microscope, particles having a particle diameter of less than 8 zm were not observed.
- the display function was evaluated using an image display device incorporating an image display panel fabricated using these particles as an image display medium. Table 9 shows the results.
- Particle group A consists of acrylic urethane resin EAU53B (manufactured by Asia Kogyo Co., Ltd.) / ⁇ PD I crosslinker Ethacell Hardener HX (manufactured by Asia Co., Ltd.) and carbon black (MA100: manufactured by Mitsubishi Chemical Corporation). 4 parts by weight and 2 parts by weight of the charge control agent Bontron NO7 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and then pulverized and classified by a jet mill. The prepared particle group A is negatively charged and has an average particle size of 5.
- Particle group B is composed of the acrylic urethane resin EAU53 B (manufactured by Asia Kogyo Co., Ltd.) / 1 PD I-based cross-linking agent Ethacell Hardener HX (manufactured by Asia Kogyo Co., Ltd.), 10 parts by weight of titanium dioxide, and Bontron charge control agent.
- E 89 made by Orient Chemical Co., Ltd. 2 weight was added and kneaded, followed by pulverization and classification using a jet mill.
- the produced particle group B was a group of white particles having a positive charge property and an average particle diameter of 11.3 ⁇ .
- the display function was evaluated using an image display device incorporating an image display panel fabricated using these particles as an image display medium. Table 9 shows the results.
- Particle group ⁇ is composed of acrylic urethane resin EAU53 B (manufactured by Asia Kogyo Co., Ltd.) / 1 PD I-based crosslinker Exel Hardener HX (manufactured by Asia Kogyo Co., Ltd.) and carbon black (MA100: 'Mitsubishi Chemical Corporation) 4 parts by weight) and 2 parts by weight of the charge control agent Bontron NO7 (manufactured by Orient Chemical Co., Ltd.) were added, kneaded, and pulverized and classified by a jet mill.
- the prepared particle group A was a black particle group having negative chargeability and an average particle diameter of 9.5 ⁇ .
- '' Particle group ⁇ is composed of acrylic urethane resin EAU53 ⁇ (manufactured by Asia Kogyo Co., Ltd.) / 1 PD I-type cross-linking agent Ethacell Hardener ⁇ (manufactured by Asia Kogyo Co., Ltd.), 10 parts by weight of titanium dioxide, and Bontron charge control agent No. 89 (manufactured by Orient Chemical Co., Ltd.) was added, kneaded, kneaded, and pulverized and classified with a jet mill.
- the prepared particle group ⁇ was a positively chargeable white particle group having an average particle diameter of 8.2 m.
- the display function was evaluated using an image display device incorporating an image display panel fabricated using these particles as an image display medium. Table 9 shows the results.
- Example 9 1 was Ddark rather Dbright
- Example 9 2 in Examples 9 3 and Example 9 4
- white reflection density is higher in the initial odor
- a classifier MD S-2: manufactured by Nippon Pneumatic Industries Co., Ltd.
- MD S-2 manufactured by Nippon Pneumatic Industries Co., Ltd.
- the overcut classification and the undercut classification were performed in Examples 92 and 93. It can be seen that the initial white reflection density was higher than that of Example 91 in which the white reflection density was not performed, and the reduction in the white reflection density and the reduction in the contrast ratio were small even after repeated inversion display.
- Example 94 since Dbright / Ddark> 2 in relation to the average particle diameter, the comparison was made between the initial white reflection density, the decrease in white reflection density after repeated inversion display, and the decrease in contrast ratio. Although the results are better than Example 91, the results are slightly inferior to the results of Examples 91 to 93 that satisfy the relationship of DbrightZDdark2. Furthermore, in Comparative Example 91 which is not Dbright and Dbright in relation to the average particle diameter, the initial white reflection density is low, and the reduction in white reflection density and the reduction in contrast ratio after repeated inversion display are large. You can see that.
- the blending ratio is such that PBT (“Toraycon 1401 X31” manufactured by Toray Industries, Inc.) as a base resin and magnesium stearate as a fatty acid metal salt ( According to a method similar to the method described above, the present invention is made from a reagent grade manufactured by Nippon Yushi Co., Ltd.) and CZB as a pigment ( ⁇ -660 ”manufactured by Asahi Carbon Co., Ltd.). The particles of Example 102 were obtained.
- the particle diameter of the particles was measured according to the method described above, and the blow-off charge of the particles was measured by the method described below. did.
- the results are shown in Table 10.
- the blow-off charge was measured as follows. That is, the principle and method of the blow-off measurement are as follows. In the blow-off method, a mixture of powder (also referred to as a particle group) and a carrier is placed in a cylindrical container having nets at both ends, and high-pressure gas is blown from one end to separate the powder and the carrier, thereby forming a net. Blow off (blow off) only the powder from the openings.
- blow-off powder charge amount measuring device TB-200 manufactured by Toshiba Chemical Corporation was used.
- F963-2535 manufactured by Powdertech Co., Ltd. is used as the carrier, and the charge density per unit weight of the particles (unit: is measured first, and the surface charge density (unit: / CZm 2 ) is determined from the average diameter and specific gravity separately obtained.
- the average diameter was calculated by the method described above, specifically, using a Mastersizer2000 (Malvern Instruments Ltd.) measuring instrument to put the particles in a nitrogen stream, and using the attached analysis software (volume using Mie theory).
- the specific gravity was measured using a Shimadzu Corp. hydrometer (trade name: Manole Tivoli Volume Densitometer H135).
- the charge amount was large, and as a result, a high reversing performance was obtained by manufacturing an f-image display panel using an image display medium using these particles. I understand.
- the white portion has a total reflectance of 70% or more at the interface between the center portion and the outer layer portion
- the outer layer is composed of at least one or more low-refractive-index materials mixed with fine particles of a high-refractive-index material. Since it is composed of the embedded resin layer, it is possible to improve the white luminance factor by having a central portion exhibiting high total reflectance. The same effect can be obtained with a white powder fluid using the white particles according to the first invention of the present invention.
- a particle group consisting of three types of particles obtained by adding a third particle to two types of substantially spherical particles having different charging characteristics is displayed as an image. Since the image display panel is enclosed between two substrates as a medium, particles are less likely to aggregate and adhere to each other, improving the durability of image display.
- particles made of a low-dielectric insulating material having a specific permittivity ⁇ r of preferably ⁇ r ⁇ 5.0 are used. Therefore, even if the particles are of the same polarity, generation of agglomerates of the particles can be eliminated, and good image display can be performed.
- a white pigment preferably a titanium oxide pigment, whose surface is coated with a binder, is agglomerated or granulated, and a large number of microbubbles are introduced into the inside.
- the hiding power (reflectance) of the white particles or the white powder fluid using the particles can be greatly improved.
- one of two kinds of particles having different charging characteristics is used for at least two or more kinds of image display media.
- one particle for example, a crushed particle
- the other one a substantially spherical particle (for example, a polymerized particle) having no macroscopic unevenness on the surface
- the two particles have different surface states (first embodiment).
- one of two kinds of particles having different charging characteristics used for at least two or more kinds of image display media is a particle having a macroscopic four-convex surface (for example, a ground particle), and the other is a substantially spherical shape having no macroscopic unevenness on the surface.
- Particles for example, polymerized particles
- fine particles having a different charge polarity from the particles having no macroscopic irregularities on the surface are attached as third particles (second embodiment), whereby the particles are aggregated and adhered to each other. It becomes difficult The durability of the image display is improved.
- the base tree Since the fat is filled with the white pigment and the hollow particles, the white particles (or powder fluid) can be improved in whiteness (white reflectance) due to the hiding effect of the hollow particles.
- the thermosetting resin subjected to the thermal crosslinking reaction is used as the base resin of the particles, the heat resistance can be improved, and as a result, the image display can be performed. Adhesion to the panel is not observed.
- at least one of the two kinds of particles having different charging characteristics and optical reflectivity used as the image display medium is formed into a flat round shape particle.
- the particles when the particles are moved and arranged on the display substrate surface, the particles are easily arranged without gaps, and the gap between the particles is reduced, so that the contrast of the image is improved.
- the two types of particles having different charging characteristics and optical reflectance used as image display media are flat round shaped particles, the particles are less likely to aggregate and adhere to each other, and at the same time the particles collide when moving. And the durability of image display is improved.
- the relationship between the color used as the image display medium and the particle size of the two types of particles having different charging characteristics is expressed by the particle size of the dark and dark color particles. Since Ddark ⁇ Dbright in Ddark and the particle diameter Dbright of the light- and bright-colored particle group, when Ddark moves in opposite directions according to the direction of the electric field between the substrates and is arranged on the display substrate surface, this The contrast is improved as compared with the case where the relationship between the particle diameters is reversed.
- the base resin of the particles contains metal oxide (MO x) (where M: Metal element, O: oxygen, X: O / M ratio) or fatty acid metal salt compound (C mH n COO) y M z (where M: metal element, m, n, y, z are integers, 4
- the above-described image display devices include a display unit of a mobile device such as a notebook computer, a PDA, a mobile phone, a handy terminal, an electronic book such as an electronic book and an electronic newspaper, a signboard, and a poster. , Blackboards and other bulletin boards, copy machines, rewriter paper instead of printer paper, displays for calculators, home appliances, automotive products, etc., card displays for point cards, IC cards, etc., electronic advertising, electronic POP, electronic It can be suitably used for price tags, electronic music scores, and display units of RF-ID devices.
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Abstract
Description
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US10/552,283 US7236291B2 (en) | 2003-04-02 | 2004-04-02 | Particle use for image display media, image display panel using the particles, and image display device |
JP2005505270A JP4579823B2 (ja) | 2003-04-02 | 2004-04-02 | 画像表示媒体に用いる粒子、それを用いた画像表示用パネル及び画像表示装置 |
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WO2005054933A2 (en) | 2003-11-26 | 2005-06-16 | E Ink Corporation | Electro-optic displays with reduced remnant voltage |
JP2006072283A (ja) * | 2004-08-02 | 2006-03-16 | Bridgestone Corp | 表示媒体用粒子及びそれを用いた情報表示用パネル、情報表示装置 |
JP2006163076A (ja) * | 2004-12-08 | 2006-06-22 | Bridgestone Corp | 表示媒体用粒子の製造方法、表示媒体用粒子及び情報表示用パネル |
WO2006081305A2 (en) | 2005-01-26 | 2006-08-03 | E Ink Corporation | Electrophoretic displays using gaseous fluids |
WO2007104003A2 (en) | 2006-03-08 | 2007-09-13 | E Ink Corporation | Methods for production of electro-optic displays |
JP2007240876A (ja) * | 2006-03-08 | 2007-09-20 | Fuji Xerox Co Ltd | 画像表示媒体 |
WO2008023498A1 (en) * | 2006-08-25 | 2008-02-28 | Brother Kogyo Kabushiki Kaisha | Electrophoretic display medium |
WO2008087794A1 (ja) * | 2007-01-17 | 2008-07-24 | Brother Kogyo Kabushiki Kaisha | 電気泳動表示媒体及び電気泳動表示装置 |
WO2008120510A1 (ja) * | 2007-03-29 | 2008-10-09 | Brother Kogyo Kabushiki Kaisha | 電気泳動表示媒体 |
EP2309322A1 (en) | 2006-09-22 | 2011-04-13 | E-Ink Corporation | Electro-optic display and materials for use therein |
JP2012042519A (ja) * | 2010-08-12 | 2012-03-01 | Hitachi Chem Co Ltd | 調光フィルム |
EP2487540A1 (en) | 2006-09-18 | 2012-08-15 | E-Ink Corporation | Color electro-optic displays |
EP2487674A2 (en) | 2003-11-05 | 2012-08-15 | E-Ink Corporation | Electro-optic displays |
EP2546693A2 (en) | 2006-12-19 | 2013-01-16 | E Ink Corporation | Electro-optic display with edge seal |
EP2555182A1 (en) | 2007-02-02 | 2013-02-06 | E Ink Corporation | Electrophoretic displays having transparent electrode and conductor connected thereto |
EP2711770A2 (en) | 2005-10-18 | 2014-03-26 | E Ink Corporation | Components for electro-optic displays |
US8928562B2 (en) | 2003-11-25 | 2015-01-06 | E Ink Corporation | Electro-optic displays, and methods for driving same |
JP2016520209A (ja) * | 2013-05-14 | 2016-07-11 | イー インク コーポレイション | 着色電気泳動ディスプレイ |
EP3067744A2 (en) | 2004-03-23 | 2016-09-14 | E Ink Corporation | Light modulators |
WO2017049020A1 (en) | 2015-09-16 | 2017-03-23 | E Ink Corporation | Apparatus and methods for driving displays |
EP3220383A1 (en) | 2012-02-01 | 2017-09-20 | E Ink Corporation | Methods for driving electro-optic displays |
US9966018B2 (en) | 2002-06-13 | 2018-05-08 | E Ink Corporation | Methods for driving electro-optic displays |
EP3505585A1 (en) | 2007-11-14 | 2019-07-03 | E Ink Corporation | Adhesives and binders for use in electro-optic assemblies |
WO2020005676A1 (en) | 2018-06-28 | 2020-01-02 | E Ink Corporation | Driving methods for variable transmission electro-phoretic media |
EP4156164A1 (en) | 2013-07-31 | 2023-03-29 | E Ink Corporation | Methods for driving electro-optic displays |
WO2023164078A1 (en) | 2022-02-25 | 2023-08-31 | E Ink Corporation | Electro-optic displays with edge seal components and methods of making the same |
WO2023200859A1 (en) | 2022-04-13 | 2023-10-19 | E Ink Corporation | Display material including patterned areas of encapsulated electrophoretic media |
WO2023211699A1 (en) | 2022-04-27 | 2023-11-02 | E Ink Corporation | Electro-optic display stacks with segmented electrodes and methods of making the same |
Families Citing this family (236)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7848006B2 (en) | 1995-07-20 | 2010-12-07 | E Ink Corporation | Electrophoretic displays with controlled amounts of pigment |
US7583251B2 (en) | 1995-07-20 | 2009-09-01 | E Ink Corporation | Dielectrophoretic displays |
US7999787B2 (en) | 1995-07-20 | 2011-08-16 | E Ink Corporation | Methods for driving electrophoretic displays using dielectrophoretic forces |
US8040594B2 (en) | 1997-08-28 | 2011-10-18 | E Ink Corporation | Multi-color electrophoretic displays |
DE69920228T2 (de) | 1998-07-08 | 2005-01-27 | E-Ink Corp., Cambridge | Verfahren zur verbesserung der farbwiedergabe in elektrophoretischen vorrichtungen, welche mikrokapseln verwenden |
US8115729B2 (en) | 1999-05-03 | 2012-02-14 | E Ink Corporation | Electrophoretic display element with filler particles |
AU2002250304A1 (en) | 2001-03-13 | 2002-09-24 | E Ink Corporation | Apparatus for displaying drawings |
US7679814B2 (en) | 2001-04-02 | 2010-03-16 | E Ink Corporation | Materials for use in electrophoretic displays |
US8390918B2 (en) | 2001-04-02 | 2013-03-05 | E Ink Corporation | Electrophoretic displays with controlled amounts of pigment |
US8582196B2 (en) * | 2001-05-15 | 2013-11-12 | E Ink Corporation | Electrophoretic particles and processes for the production thereof |
US7535624B2 (en) | 2001-07-09 | 2009-05-19 | E Ink Corporation | Electro-optic display and materials for use therein |
US9530363B2 (en) | 2001-11-20 | 2016-12-27 | E Ink Corporation | Methods and apparatus for driving electro-optic displays |
US8558783B2 (en) | 2001-11-20 | 2013-10-15 | E Ink Corporation | Electro-optic displays with reduced remnant voltage |
US8593396B2 (en) | 2001-11-20 | 2013-11-26 | E Ink Corporation | Methods and apparatus for driving electro-optic displays |
US9412314B2 (en) | 2001-11-20 | 2016-08-09 | E Ink Corporation | Methods for driving electro-optic displays |
US7223672B2 (en) | 2002-04-24 | 2007-05-29 | E Ink Corporation | Processes for forming backplanes for electro-optic displays |
US9470950B2 (en) | 2002-06-10 | 2016-10-18 | E Ink Corporation | Electro-optic displays, and processes for the production thereof |
US8049947B2 (en) | 2002-06-10 | 2011-11-01 | E Ink Corporation | Components and methods for use in electro-optic displays |
US8363299B2 (en) | 2002-06-10 | 2013-01-29 | E Ink Corporation | Electro-optic displays, and processes for the production thereof |
US7843621B2 (en) | 2002-06-10 | 2010-11-30 | E Ink Corporation | Components and testing methods for use in the production of electro-optic displays |
EP3056941B1 (en) | 2002-09-03 | 2019-01-09 | E Ink Corporation | Electro-phoretic medium |
US7839564B2 (en) | 2002-09-03 | 2010-11-23 | E Ink Corporation | Components and methods for use in electro-optic displays |
US20130063333A1 (en) | 2002-10-16 | 2013-03-14 | E Ink Corporation | Electrophoretic displays |
US7910175B2 (en) | 2003-03-25 | 2011-03-22 | E Ink Corporation | Processes for the production of electrophoretic displays |
US10726798B2 (en) | 2003-03-31 | 2020-07-28 | E Ink Corporation | Methods for operating electro-optic displays |
US20110164301A1 (en) | 2003-11-05 | 2011-07-07 | E Ink Corporation | Electro-optic displays, and materials for use therein |
US8177942B2 (en) | 2003-11-05 | 2012-05-15 | E Ink Corporation | Electro-optic displays, and materials for use therein |
US7672040B2 (en) | 2003-11-05 | 2010-03-02 | E Ink Corporation | Electro-optic displays, and materials for use therein |
US8289250B2 (en) * | 2004-03-31 | 2012-10-16 | E Ink Corporation | Methods for driving electro-optic displays |
US11250794B2 (en) | 2004-07-27 | 2022-02-15 | E Ink Corporation | Methods for driving electrophoretic displays using dielectrophoretic forces |
KR100700523B1 (ko) * | 2005-02-11 | 2007-03-29 | 엘지전자 주식회사 | 충돌 대전형 전자종이 표시소자 및 그 제조 방법 |
US7700984B2 (en) * | 2005-05-20 | 2010-04-20 | Semiconductor Energy Laboratory Co., Ltd | Semiconductor device including memory cell |
ATE493686T1 (de) * | 2005-05-27 | 2011-01-15 | Koninkl Philips Electronics Nv | Stabiles multipartikelsystem für elektrophoretische farbanzeigen mit sehr niedrigen antriebsspannungen und mit geringem elektrolytgehalt |
WO2007002452A2 (en) | 2005-06-23 | 2007-01-04 | E Ink Corporation | Edge seals and processes for electro-optic displays |
US20080043318A1 (en) | 2005-10-18 | 2008-02-21 | E Ink Corporation | Color electro-optic displays, and processes for the production thereof |
US7843624B2 (en) | 2006-03-08 | 2010-11-30 | E Ink Corporation | Electro-optic displays, and materials and methods for production thereof |
US8390301B2 (en) | 2006-03-08 | 2013-03-05 | E Ink Corporation | Electro-optic displays, and materials and methods for production thereof |
US8610988B2 (en) | 2006-03-09 | 2013-12-17 | E Ink Corporation | Electro-optic display with edge seal |
US7952790B2 (en) | 2006-03-22 | 2011-05-31 | E Ink Corporation | Electro-optic media produced using ink jet printing |
US7903319B2 (en) | 2006-07-11 | 2011-03-08 | E Ink Corporation | Electrophoretic medium and display with improved image stability |
US8018640B2 (en) | 2006-07-13 | 2011-09-13 | E Ink Corporation | Particles for use in electrophoretic displays |
US7986450B2 (en) | 2006-09-22 | 2011-07-26 | E Ink Corporation | Electro-optic display and materials for use therein |
US8144386B2 (en) * | 2006-09-22 | 2012-03-27 | Bridgestone Corporation | Particles for display media and information display panel using same |
US7649666B2 (en) | 2006-12-07 | 2010-01-19 | E Ink Corporation | Components and methods for use in electro-optic displays |
KR101256709B1 (ko) | 2007-01-22 | 2013-04-19 | 이 잉크 코포레이션 | 전기-광학 디스플레이에서 사용하기 위한 다층 시트 |
US7688497B2 (en) | 2007-01-22 | 2010-03-30 | E Ink Corporation | Multi-layer sheet for use in electro-optic displays |
US8074804B2 (en) * | 2007-02-14 | 2011-12-13 | Wisconsin Electric Power Company | Separation of cenospheres from fly ash |
US7826129B2 (en) | 2007-03-06 | 2010-11-02 | E Ink Corporation | Materials for use in electrophoretic displays |
ATE507267T1 (de) * | 2007-04-13 | 2011-05-15 | Asahi Glass Co Ltd | Verfahren zur herstellung einer mit hydrophobiertem siliziumoxid belegter metalloxidpartikel |
KR20130130871A (ko) | 2007-05-21 | 2013-12-02 | 이 잉크 코포레이션 | 비디오 전기 광학 디스플레이를 구동하는 방법 |
US9199441B2 (en) | 2007-06-28 | 2015-12-01 | E Ink Corporation | Processes for the production of electro-optic displays, and color filters for use therein |
US8034209B2 (en) | 2007-06-29 | 2011-10-11 | E Ink Corporation | Electro-optic displays, and materials and methods for production thereof |
US8902153B2 (en) | 2007-08-03 | 2014-12-02 | E Ink Corporation | Electro-optic displays, and processes for their production |
JP5314997B2 (ja) * | 2007-11-19 | 2013-10-16 | セイコーエプソン株式会社 | 表示装置、表示装置の製造方法および電子機器 |
WO2009117730A1 (en) | 2008-03-21 | 2009-09-24 | E Ink Corporation | Electro-optic displays and color filters |
JP2009244551A (ja) * | 2008-03-31 | 2009-10-22 | Konica Minolta Business Technologies Inc | 画像表示装置用表示粒子および画像表示装置 |
EP2277162B1 (en) | 2008-04-11 | 2020-08-26 | E Ink Corporation | Methods for driving electro-optic displays |
WO2009129217A2 (en) | 2008-04-14 | 2009-10-22 | E Ink Corporation | Methods for driving electro-optic displays |
JP2010009956A (ja) * | 2008-06-27 | 2010-01-14 | Panasonic Corp | 導光シート及びこれを用いた可動接点体 |
EP2214053A4 (en) * | 2008-08-05 | 2010-10-27 | Bridgestone Corp | PARTICLE FOR A DISPLAY MEDIUM AND INFORMATION PANEL THEREFORE |
US8517251B2 (en) * | 2008-08-29 | 2013-08-27 | The Invention Science Fund I, Llc | Application control based on flexible interface conformation sequence status |
US9176637B2 (en) * | 2008-08-29 | 2015-11-03 | Invention Science Fund I, Llc | Display control based on bendable interface containing electronic device conformation sequence status |
US8235280B2 (en) * | 2008-08-29 | 2012-08-07 | The Invention Science Fund I, Llc | E-paper display control of classified content based on E-paper conformation |
US8613394B2 (en) * | 2008-08-29 | 2013-12-24 | The Invention Science Fund I, Llc | Bendable electronic interface external control system and method |
US8446357B2 (en) * | 2008-10-07 | 2013-05-21 | The Invention Science Fund I, Llc | E-paper display control based on conformation sequence status |
US8500002B2 (en) | 2008-08-29 | 2013-08-06 | The Invention Science Fund I, Llc | Display control based on bendable display containing electronic device conformation sequence status |
US8466870B2 (en) * | 2008-08-29 | 2013-06-18 | The Invention Science Fund, I, LLC | E-paper application control based on conformation sequence status |
US8596521B2 (en) * | 2008-08-29 | 2013-12-03 | The Invention Science Fund I, Llc | E-paper display control based on conformation sequence status |
US8511563B2 (en) | 2008-08-29 | 2013-08-20 | The Invention Science Fund I, Llc | Display control of classified content based on flexible interface E-paper conformation |
US8462104B2 (en) | 2008-08-29 | 2013-06-11 | The Invention Science Fund I, Llc | E-paper display control based on conformation sequence status |
US8240548B2 (en) * | 2008-08-29 | 2012-08-14 | The Invention Science Fund I, Llc | Display control of classified content based on flexible display containing electronic device conformation |
US8251278B2 (en) * | 2008-08-29 | 2012-08-28 | The Invention Science Fund I, Llc | Display control based on bendable display containing electronic device conformation sequence status |
US8490860B2 (en) * | 2008-08-29 | 2013-07-23 | The Invention Science Fund I, Llc | Display control of classified content based on flexible display containing electronic device conformation |
US8272571B2 (en) * | 2008-08-29 | 2012-09-25 | The Invention Science Fund I, Llc | E-paper display control of classified content based on e-paper conformation |
US8485426B2 (en) * | 2008-08-29 | 2013-07-16 | The Invention Science Fund I, Llc | Bendable electronic device status information system and method |
US8297495B2 (en) * | 2008-08-29 | 2012-10-30 | The Invention Science Fund I, Llc | Application control based on flexible interface conformation sequence status |
US9035870B2 (en) * | 2008-10-07 | 2015-05-19 | The Invention Science Fund I, Llc | E-paper display control based on conformation sequence status |
US8777099B2 (en) * | 2008-08-29 | 2014-07-15 | The Invention Science Fund I, Llc | Bendable electronic device status information system and method |
US20100073334A1 (en) * | 2008-09-25 | 2010-03-25 | Cohen Alexander J | E-paper application control based on conformation sequence status |
US8393531B2 (en) * | 2008-08-29 | 2013-03-12 | The Invention Science Fund I, Llc | Application control based on flexible electronic device conformation sequence status |
US8646693B2 (en) | 2008-08-29 | 2014-02-11 | The Invention Science Fund I, Llc | Application control based on flexible electronic device conformation sequence status |
US8708220B2 (en) * | 2008-08-29 | 2014-04-29 | The Invention Science Fund I, Llc | Display control based on bendable interface containing electronic device conformation sequence status |
US8624833B2 (en) * | 2008-09-11 | 2014-01-07 | The Invention Science Fund I, Llc | E-paper display control of classified content based on e-paper conformation |
US20100073263A1 (en) * | 2008-09-22 | 2010-03-25 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware, | E-Paper application control based on conformation sequence status |
US8866731B2 (en) * | 2008-08-29 | 2014-10-21 | The Invention Science Fund I, Llc | E-paper display control of classified content based on e-paper conformation |
US8584930B2 (en) * | 2008-11-07 | 2013-11-19 | The Invention Science Fund I, Llc | E-paper display control based on conformation sequence status |
US8279199B2 (en) * | 2008-11-14 | 2012-10-02 | The Invention Science Fund I, Llc | E-paper external control system and method |
US8544722B2 (en) * | 2008-08-29 | 2013-10-01 | The Invention Science Fund I, Llc | Bendable electronic interface external control system and method |
US8493336B2 (en) * | 2008-10-10 | 2013-07-23 | The Invention Science Fund I, Llc | E-paper display control based on conformation sequence status |
US8322599B2 (en) * | 2008-08-29 | 2012-12-04 | The Invention Science Fund I, Llc | Display control of classified content based on flexible interface e-paper conformation |
TWI484273B (zh) | 2009-02-09 | 2015-05-11 | E Ink Corp | 電泳粒子 |
US8098418B2 (en) | 2009-03-03 | 2012-01-17 | E. Ink Corporation | Electro-optic displays, and color filters for use therein |
JP5134637B2 (ja) * | 2009-03-13 | 2013-01-30 | 三菱鉛筆株式会社 | 電気泳動表示用液、それを用いた電気泳動表示装置及び電子機器 |
TW201102735A (en) * | 2009-07-02 | 2011-01-16 | Wintek Corp | Display medium and electrophoretic display |
KR101089872B1 (ko) * | 2009-09-18 | 2011-12-05 | 삼성전기주식회사 | 전자종이 디스플레이 장치 및 제조방법 |
US8754859B2 (en) | 2009-10-28 | 2014-06-17 | E Ink Corporation | Electro-optic displays with touch sensors and/or tactile feedback |
US8654436B1 (en) | 2009-10-30 | 2014-02-18 | E Ink Corporation | Particles for use in electrophoretic displays |
US9620066B2 (en) | 2010-02-02 | 2017-04-11 | E Ink Corporation | Method for driving electro-optic displays |
US8446664B2 (en) | 2010-04-02 | 2013-05-21 | E Ink Corporation | Electrophoretic media, and materials for use therein |
WO2011127462A2 (en) | 2010-04-09 | 2011-10-13 | E Ink Corporation | Methods for driving electro-optic displays |
TWI484275B (zh) | 2010-05-21 | 2015-05-11 | E Ink Corp | 光電顯示器及其驅動方法、微型空腔電泳顯示器 |
WO2011153297A2 (en) | 2010-06-02 | 2011-12-08 | E Ink Corporation | Color electro-optic displays |
US8797634B2 (en) | 2010-11-30 | 2014-08-05 | E Ink Corporation | Multi-color electrophoretic displays |
US8873129B2 (en) | 2011-04-07 | 2014-10-28 | E Ink Corporation | Tetrachromatic color filter array for reflective display |
WO2012162095A2 (en) | 2011-05-21 | 2012-11-29 | E Ink Corporation | Electro-optic displays |
US11030936B2 (en) | 2012-02-01 | 2021-06-08 | E Ink Corporation | Methods and apparatus for operating an electro-optic display in white mode |
US10190743B2 (en) | 2012-04-20 | 2019-01-29 | E Ink Corporation | Illumination systems for reflective displays |
US11467466B2 (en) | 2012-04-20 | 2022-10-11 | E Ink Corporation | Illumination systems for reflective displays |
JP5935064B2 (ja) | 2012-05-31 | 2016-06-15 | イー インク コーポレイション | 画像表示媒体の駆動装置、画像表示装置、及び駆動プログラム |
US10282033B2 (en) | 2012-06-01 | 2019-05-07 | E Ink Corporation | Methods for updating electro-optic displays when drawing or writing on the display |
US9513743B2 (en) | 2012-06-01 | 2016-12-06 | E Ink Corporation | Methods for driving electro-optic displays |
CN104583853B (zh) | 2012-07-27 | 2018-01-26 | 伊英克公司 | 用于生产电光显示器的工艺 |
US10037735B2 (en) | 2012-11-16 | 2018-07-31 | E Ink Corporation | Active matrix display with dual driving modes |
US9715155B1 (en) | 2013-01-10 | 2017-07-25 | E Ink Corporation | Electrode structures for electro-optic displays |
WO2014110394A1 (en) | 2013-01-10 | 2014-07-17 | E Ink Corporation | Electro-optic display with controlled electrochemical reactions |
US9436056B2 (en) | 2013-02-06 | 2016-09-06 | E Ink Corporation | Color electro-optic displays |
US9195111B2 (en) | 2013-02-11 | 2015-11-24 | E Ink Corporation | Patterned electro-optic displays and processes for the production thereof |
US9721495B2 (en) | 2013-02-27 | 2017-08-01 | E Ink Corporation | Methods for driving electro-optic displays |
CN110610687B (zh) | 2013-03-01 | 2022-07-12 | 伊英克公司 | 用于驱动电光显示器的方法 |
KR20140131669A (ko) * | 2013-05-06 | 2014-11-14 | 삼성전자주식회사 | 반사형 디스플레이 장치 |
US9620048B2 (en) | 2013-07-30 | 2017-04-11 | E Ink Corporation | Methods for driving electro-optic displays |
JP6205985B2 (ja) * | 2013-08-23 | 2017-10-04 | ソニー株式会社 | 表示装置 |
EP3470915B1 (en) | 2013-10-22 | 2021-08-25 | E Ink Corporation | A wide operating temperature range electrophoretic device |
KR101883582B1 (ko) | 2014-01-17 | 2018-07-30 | 이 잉크 코포레이션 | 2상의 전극층을 갖는 전기광학 디스플레이 |
CN106103600B (zh) | 2014-02-06 | 2019-10-29 | 伊英克公司 | 电泳粒子及其制备方法 |
US10317767B2 (en) | 2014-02-07 | 2019-06-11 | E Ink Corporation | Electro-optic display backplane structure with drive components and pixel electrodes on opposed surfaces |
US9671635B2 (en) | 2014-02-07 | 2017-06-06 | E Ink Corporation | Electro-optic display backplane structures with drive components and pixel electrodes on opposed surfaces |
US10446585B2 (en) | 2014-03-17 | 2019-10-15 | E Ink Corporation | Multi-layer expanding electrode structures for backplane assemblies |
US9953588B1 (en) | 2014-03-25 | 2018-04-24 | E Ink Corporation | Nano-particle based variable transmission devices |
US10657869B2 (en) | 2014-09-10 | 2020-05-19 | E Ink Corporation | Methods for driving color electrophoretic displays |
KR102061435B1 (ko) | 2014-09-10 | 2019-12-31 | 이 잉크 코포레이션 | 착색 전기영동 디스플레이들 |
EP3198861A4 (en) | 2014-09-26 | 2018-04-11 | E Ink Corporation | Color sets for low resolution dithering in reflective color displays |
WO2016073914A1 (en) | 2014-11-07 | 2016-05-12 | E Ink Corporation | Applications of electro-optic displays |
US10197883B2 (en) | 2015-01-05 | 2019-02-05 | E Ink Corporation | Electro-optic displays, and methods for driving same |
EP3243105A4 (en) | 2015-01-05 | 2018-08-08 | E Ink Corporation | Electro-optic displays, and methods for driving same |
US9835925B1 (en) | 2015-01-08 | 2017-12-05 | E Ink Corporation | Electro-optic displays, and processes for the production thereof |
EP3254276A4 (en) | 2015-02-04 | 2018-07-11 | E Ink Corporation | Electro-optic displays with reduced remnant voltage, and related apparatus and methods |
JP6814149B2 (ja) | 2015-02-04 | 2021-01-13 | イー インク コーポレイション | 暗モードおよび明モードで表示する電気光学ディスプレイおよび関連する装置及び方法 |
WO2016133949A1 (en) | 2015-02-17 | 2016-08-25 | E Ink Corporation | Electromagnetic writing apparatus for electro-optic displays |
US9880646B2 (en) | 2015-02-18 | 2018-01-30 | E Ink Corporation | Addressable electro-optic display |
US10040954B2 (en) | 2015-05-28 | 2018-08-07 | E Ink California, Llc | Electrophoretic medium comprising a mixture of charge control agents |
JP6524271B2 (ja) | 2015-06-29 | 2019-06-05 | イー インク コーポレイション | ディスプレイ電極への機械的および電気的接続のための方法 |
ES2974101T3 (es) | 2015-06-30 | 2024-06-25 | E Ink Corp | Pantallas electroforéticas compuestas |
CN107849174B (zh) | 2015-07-23 | 2021-02-02 | 伊英克公司 | 用于电光介质的聚合物制剂 |
US11287718B2 (en) | 2015-08-04 | 2022-03-29 | E Ink Corporation | Reusable display addressable with incident light |
JP6571276B2 (ja) | 2015-08-31 | 2019-09-04 | イー インク コーポレイション | 描画デバイスの電子的な消去 |
US10803813B2 (en) | 2015-09-16 | 2020-10-13 | E Ink Corporation | Apparatus and methods for driving displays |
US11657774B2 (en) | 2015-09-16 | 2023-05-23 | E Ink Corporation | Apparatus and methods for driving displays |
EP3356445B1 (en) | 2015-09-30 | 2021-01-06 | E Ink Corporation | Polyurethane adhesive layers for electro-optic assemblies |
JP6552751B2 (ja) | 2015-10-06 | 2019-07-31 | イー インク コーポレイション | 改良された低温電気泳動媒体 |
ES2848473T3 (es) | 2015-11-11 | 2021-08-09 | E Ink Corp | Pigmentos de quinacridona funcionalizados |
US10795233B2 (en) | 2015-11-18 | 2020-10-06 | E Ink Corporation | Electro-optic displays |
US10061123B2 (en) | 2016-01-17 | 2018-08-28 | E Ink California, Llc | Surfactants for improving electrophoretic media performance |
US9765015B2 (en) | 2016-01-17 | 2017-09-19 | E Ink California, Llc | Branched polyol additives for electrophoretic media |
KR102250635B1 (ko) | 2016-02-08 | 2021-05-10 | 이 잉크 코포레이션 | 화이트 모드에서 전기-광학 디스플레이를 동작시키기 위한 방법들 및 장치들 |
US10254620B1 (en) | 2016-03-08 | 2019-04-09 | E Ink Corporation | Encapsulated photoelectrophoretic display |
EP3427254A4 (en) | 2016-03-09 | 2020-02-26 | E Ink Corporation | METHOD FOR CONTROLLING ELECTRO-OPTICAL DISPLAYS |
US10593272B2 (en) | 2016-03-09 | 2020-03-17 | E Ink Corporation | Drivers providing DC-balanced refresh sequences for color electrophoretic displays |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002139750A (ja) * | 2000-11-02 | 2002-05-17 | Fuji Xerox Co Ltd | 画像表示媒体、画像表示装置及び画像表示方法 |
JP2002236471A (ja) * | 2001-02-07 | 2002-08-23 | Fuji Xerox Co Ltd | 画像表示装置 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5189337A (en) * | 1988-09-09 | 1993-02-23 | Hitachi, Ltd. | Ultrafine particles for use in a cathode ray tube or an image display face plate |
-
2004
- 2004-04-02 JP JP2005505270A patent/JP4579823B2/ja not_active Expired - Fee Related
- 2004-04-02 US US10/552,283 patent/US7236291B2/en not_active Expired - Fee Related
- 2004-04-02 WO PCT/JP2004/004854 patent/WO2004090626A1/ja active Application Filing
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002139750A (ja) * | 2000-11-02 | 2002-05-17 | Fuji Xerox Co Ltd | 画像表示媒体、画像表示装置及び画像表示方法 |
JP2002236471A (ja) * | 2001-02-07 | 2002-08-23 | Fuji Xerox Co Ltd | 画像表示装置 |
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Also Published As
Publication number | Publication date |
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JP4579823B2 (ja) | 2010-11-10 |
JPWO2004090626A1 (ja) | 2006-07-06 |
US20060146394A1 (en) | 2006-07-06 |
US7236291B2 (en) | 2007-06-26 |
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