Microcapsule for electrophoretic display device, process for manufacturing the same and use thereof
An electrophoretic display and microcapsule technology, which is applied in microcapsule preparations, microsphere preparation, instruments, etc., can solve problems such as contrast reduction, and achieve the effect of inhibiting subsequent contrast reduction.
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[0122] The second method of the present invention for preparing microcapsules for electrophoretic display elements (hereinafter referred to as the second preparation method of the present invention), as described above, comprises causing microcapsules for electrophoretic display elements and ion exchange resins to dissolve in an aqueous medium. Coexisting step (A) is a method as a basic step, wherein the microcapsule includes electrophoretic particles and a solvent, both of which are encapsulated in a shell. In detail, the above-mentioned step (A) is to cause microcapsules for electrophoretic display elements (wherein the microcapsules are obtained by the step of microencapsulating (to be the core substance) dispersion liquid for electrophoretic display elements) and ion exchange resin in an aqueous medium Coexistence steps.
[0123] The second production method of the present invention is not limited except that step (A) is included as a basic step, and all methods (such as v...
Embodiment 1-1
[0204] Into a 300 ml detachable flask, 14.5 g of polyethyleneimine (product name: Epomin SP006 (Mw=600), manufactured by Nippon Shokubai Co., Ltd.) and 43.5 g of water were initially introduced, and after that, the mixture was stirred for 10 minutes. 97.2 g of an aqueous solution of an epoxy compound (lauryl polyoxyethylene (n=22) glycidyl ester, solubility in water: 100%) prepared in advance 97.2 g was added dropwise.
[0205] While maintaining the temperature of the liquid in the flask at 25°C or lower, dropwise addition was performed, stirring was continued for 30 minutes after the addition was complete, and then the temperature was raised to 70°C and kept at this temperature for 2 hours, and it was Cooling to normal temperature afforded compound (A1) having a dispersity of 25% by weight of solid component content.
Embodiment 1-2
[0207] According to the same method as in Synthesis Example 1-1, the difference is that after the initial charge in Synthesis Example 1-1, 130.4 g of 25wt% which had been prepared in advance was added dropwise within 10 minutes under stirring An aqueous solution of an epoxy compound (lauryl polyoxyethylene (n=44) glycidyl ester, solubility in water: 100%) obtained compound (A2) having a dispersity of 25 wt% solid component content.
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