Curing resin composition and sealants and end-sealing materials for displays
a technology of resin composition and sealant, applied in the direction of instruments, non-linear optics, other chemical processes, etc., can solve the problem of inferior humidity resistance, and achieve the effect of excellent storage stability
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example 2
[0156] A sealant was obtained in the same manner as Example 1, except that partly acrylated propyleneoxide product obtained as (B) 20 parts by weight was used in place of the urethane-modified partly acylated product obtained as (C) 20 parts by weight and a hydrazide type curing agent (NDH, produced by Japan Hydrazine Co., Inc.) 15 parts by weight was used in place of the hydrazide type curing agent (Amicure VDH, produced by Ajinomoto Fine Techno Co., Inc.) 15 parts by weight and using the sealant, a liquid crystal display cell was fabricated.
example 3
(Synthesis of Benzoin Ether Compound A)
[0174] Potassium hydroxide 0.4 g was dissolved in ethanol 5 mL and dimethyl sulfoxide 200 mL was further added to obtain a solution. Benzoin methyl ether 30 g (0.13 mol) was dissolved in the solution and paraformaldehyde 5 g (0.16 mol) was added and reacted at 40° C. for 3 hours under nitrogen current. After that, the reaction product was cooled to a room temperature and neutralized with a dilute hydrochloric acid and then saturated salt water 120 mL was added. The solution was extracted by ethyl acetate and the extracted liquid was washed with saturated salt water three times. The washed product was dried and concentrated by anhydrous magnesium sulfate and recrystallized by diethyl ether. α-methylol benzoin methyl ether (MBME) was obtained in such a manner.
[0175] The obtained MBME was reacted with an equimolar amount of tolylene diisocyanate at 60° C. for 1 hour in the presence of dibutyl tin dilauryl in a catalytic amount and then 2-hydrox...
example 4
(Synthesis of Benzoin Ether Compound B)
[0176]α-2-carboxyethyl-benzoine methyl ether (BAE-CO2H) was obtained in the same manner as that for production of the benzoin ether compound A, except that acrylic acid was used in place of the paraformaldehyde. Glycidyl methacrylate in an amount equivalent by mole and trimethylamine in a catalytic amount were added to the obtained BAE-CO2H and reaction was carried out at 80° C. for 4 hours to obtain a benzoin ether compound B shown as follows.
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