Liquid crystal sealing compound and liquid crystal display unit using the liquid crystal sealing compound
A technology of liquid crystal display unit and liquid crystal sealant, which is applied in the directions of adhesive additives, polymer adhesive additives, non-polymer adhesive additives, etc. Realization and other problems, to achieve the effect of low liquid crystal pollution and excellent general characteristics
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[0118] Hereinafter, the present invention will be described in further detail through examples, but the present invention is not limited to the examples. In addition, unless otherwise stated, "part" and "%" herein are mass basis.
Synthetic example 1
[0119] [Synthesis Example 1: Synthesis of full acryloyl compound of bisphenol A epoxy resin]
[0120] 282.5g bisphenol A type epoxy resin (product name: YD-8125, Nippon Steel Chemical Co., Ltd. manufacture) is dissolved in 266.8g toluene, adds 0.8g therein as the dibutyl hydroxytoluene of polymerization inhibitor, and The temperature was raised to 60°C. Then, 117.5 g of 100% equivalent of epoxy group acrylic acid was added, the temperature was further raised to 80° C., 0.6 g of trimethylammonium chloride was added as a reaction catalyst, and stirred at 98° C. for about 30 hours to obtain a reaction liquid. This reaction liquid was washed with water, and toluene was distilled off to obtain 395 g of the target bisphenol A type epoxy acrylate.
Synthetic example 2
[0121] [Synthesis Example 2: Synthesis of Partial Acryloyl Compound of Bisphenol A-type Epoxy Resin]
[0122] 836 g of bisphenol A epoxy resin (RE-310S manufactured by Nippon Kayaku Co., Ltd.) was dissolved in 1000 g of toluene, 3 g of dibutylhydroxytoluene was added as a polymerization inhibitor, and the temperature was raised to 60°C. Then, 165 g of acrylic acid (manufactured by Nippon Shokubai Co., Ltd.) and 5 g of a 40% aqueous solution of tripropylammonium hydroxide as a reaction catalyst were added with 50% equivalents of epoxy groups, and stirred at 98° C. for about 10 hours to obtain The reaction solution. This reaction liquid was washed with water, and toluene was distilled off to obtain 995 g of the intended partially acryloylated bisphenol A epoxy resin.
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Abstract
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