Electrolysis solution and electrolytic capacitor using the same
A technology of electrolyte and electrolyte, which is applied in the direction of electrolytic capacitors, capacitors, circuits, etc., and can solve problems such as open circuits of capacitors
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manufacture example 1
[0078] [Manufacture of 1,2,3,4-tetramethylimidazolinium 4-methylphthalate (A-1)]
[0079] In a 1 L stirred autoclave made of SUS, 270.0 g of dimethyl carbonate and 98-0 g of 1,2,4-trimethylimidazoline were filled and reacted at a reaction temperature of 130° C. for 24 hours. After the reaction, the autoclave was cooled, and the reaction solution was analyzed by liquid chromatography. The conversion rate of 1,2,4-trimethylimidazoline was 95.0%. Unreacted materials and by-product methanol produced during the reaction were distilled off to obtain 180 g of 1,2,3,4-tetramethylimidazolinium methyl carbonate (a-1). Next, 30.0 g of the obtained 1,2,3,4-tetramethylimidazolinium methyl carbonate was dissolved in 200.0 g of methanol, and 78.6 g of 4-methylphthalic acid was slowly added, and the reaction was violent, resulting in carbon dioxide gas. Deaeration was performed at 80° C. / 20 mmHg to remove methanol to obtain 48.0 g of 1,2,3,4-tetramethylimidazolinium·4-methylphthalate (A-1)....
manufacture example 2
[0081] [Manufacture of 1,2,3,4-tetramethylimidazolinium 4-ethylphthalate (A-2)]
[0082] Except that 84.7 g of 4-ethylphthalic acid was used instead of 78.6 g of 4-methylphthalic acid, the same procedure as in Production Example 1 was carried out to obtain 1,2,3,4-tetramethylimidazolinium 4- 50.2 g of ethyl phthalate (A-2).
manufacture example 3
[0084] [Manufacture of 1,2,3,4-tetramethylimidazolinium 4-methoxyphthalate (A-3)]
[0085] Except that 85.6 g of 4-methoxyphthalic acid was used instead of 78.6 g of 4-methylphthalic acid, 1,2,3,4-tetramethylimidazolinium 4 was obtained in the same manner as in Production Example 1. - 50.5 g of methoxyphthalate (A-3).
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