JP2910073B2 - Electrolyte for driving electrolytic capacitors - Google Patents

Description

Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrolytic solution for driving an electrolytic capacitor used for an electrolytic capacitor for medium and high pressures.

2. Description of the Related Art As a conventional electrolytic solution for driving an electrolytic capacitor, particularly as a medium-to-high pressure electrolytic solution, as shown in Japanese Patent Publication No. 60-13293, an example using butyloctane diacid as a solute, As shown in Japanese Patent No. 15738, there are many cases in which 5,6-decanedicarboxylic acid is used as a solute, but it is necessary to improve the specific resistance change of the driving electrolyte at a high temperature. In order to solve such a drawback, the main solvent is γ-butyrolactone, and by using these dibasic acids or salts thereof, there is no esterification reaction even at a high temperature, and the driving resistance hardly changes in specific resistance. It becomes an electrolyte.

Problems to be Solved by the Invention However, by using these dibasic acids or salts thereof in a solvent mainly composed of γ-butyrolactone, it was good in that the change in specific resistance was difficult, but it was good for constant current formation. There is a disadvantage that the formation / discharge characteristics (hereinafter referred to as spark generation voltage) at the time are not sufficient.

SUMMARY OF THE INVENTION An object of the present invention is to provide an electrolytic solution for driving an electrolytic capacitor that solves such problems.

Means for Solving the Problems To solve the above problems, the electrolytic solution for driving an electrolytic capacitor of the present invention comprises a solvent mainly composed of γ-butyrolactone, 1-methyl-1,7-heptanedicarboxylic acid, 1,7 -Dimethyl-1,7-heptanedicarboxylic acid, 1,3-dimethyl-
1,3,9-nonanetricarboxylic acid, 1,3-dimethyl-3-carbomethoxy-1,9-nonanedicarboxylic acid, 1,3-dimethyl-1,7-heptanedicarboxylic acid, 1-methyl-3-ethyl -1,7-heptanedicarboxylic acid, 7-ethyl-1,16
-Hexadecanedicarboxylic acid, 7,8,11,12-tetramethyl-1,18-octadecanedicarboxylic acid, 7,8-dimethyl-1,14-tetradecanedicarboxylic acid, 1-methyl-1,6
-Hexanedicarboxylic acid, 1,3-dimethyl-3-carbomethoxy-1,8-octanedicarboxylic acid, 1,3-dimethyl-1,3,8-octanetricarboxylic acid, 1-methyl-1,8-
Octanedicarboxylic acid, 1,3-dimethyl-3-carbomethoxy-1,10-decanedicarboxylic acid, 1,3-dimethyl-
1,3,10-decanetricarboxylic acid, 7-phenyl-7-methoxy-1-octanecarboxylic acid, 6-phenyl-6-
An acid selected from methoxy-heptanecarboxylic acid and 6-ethyl-1,14-tetradecanedicarboxylic acid, or one or more of its salts dissolved as a main solute.

Examples of the above salts include secondary amine salts, tertiary amine salts, and quaternary ammonium salts. Specific examples of the secondary amine salts include dimethylamine salt, diethylamine salt, dipropylamine salt, and dibutylamine. Salt, methylethylamine salt, methylpropylamine salt, methylbutylamine salt, ethylpropylamine salt, ethylbutylamine salt, propylbutylamine salt. Specific examples of the tertiary amine salt include trimethylamine salt, dimethylethylamine salt, dimethylpropylamine salt, dimethylbutylamine salt, diethylmethylamine salt, methylethylpropylamine salt, methylethylbutylamine salt, dipropylmethylamine salt, methyl Propylbutylamine salt, dibutylmethylamine salt, triethylamine salt, diethylpropylamine salt, diethylbutylamine salt, dipropylethylamine salt, ethylpropylbutylamine salt, dibutylethylamine salt, tripropylamine salt, dipropylbutylamine salt, dibutylpropylamine salt, Tributylamine salts. Specific examples of the quaternary ammonium salt include tetramethylammonium salt, trimethylethylammonium salt, trimethylpropylammonium salt, trimethylbutylammonium salt, dimethyldiethylammonium salt, dimethylethylpropylammonium salt, dimethylethylbutylammonium salt, and dimethylethylammonium salt. Dipropyl ammonium salt, dimethylpropyl butyl ammonium salt, dimethyl dibutyl ammonium salt, triethyl methyl ammonium salt, diethyl methyl propyl ammonium salt, diethyl methyl butyl ammonium salt, dipropyl methyl ethyl ammonium salt, methyl ethyl propyl butyl ammonium salt, dibutyl methyl ethyl Ammonium salt, tripropylmethylammonium salt, dipropylmethylbutylammonium Umushio, dibutyl methylpropyl ammonium salt, tributyl ammonium salt, tetraethyl ammonium salt, triethyl propyl ammonium salt,
Triethylbutylammonium salt, diethyldipropylammonium salt, diethylpropylbutylammonium salt, diethyldibutylammonium salt, tripropylethylammonium salt, dipropylethylbutylammonium salt, dibutylethylpropylammonium salt, tributylethylammonium salt, tetrapropylammonium salt , Tripropylbutylammonium salt, dipropyldibutylammonium salt and tributylpropylammonium salt.

As the solvent, BLG alone or a mixture thereof is used. Examples of the solvent to be mixed include ethylene glycol, diethylene glycol, and NN-dimethylformamide, and ethylene glycol is particularly preferable.

The structural formula of the acid used in the present invention is as follows.

Action The acid used in the electrolytic solution for driving an electrolytic capacitor of the present invention described above is superior in chemical conversion property as compared with butyloctane diacid and 5,6-decanedicarboxylic acid, and thus can increase the spark generation voltage. it can.

Examples Hereinafter, examples of the present invention will be described. First, Table 1 shows a comparison of characteristics of the composition and the specific resistance, the spark generation voltage, and the water content between the conventional example and the example of the present invention.

Among the electrolytes shown in Table 1, Conventional Examples 2 and 3 and Examples
Electrolytic capacitors using 1,16,23 electrolytes (rated 400V2
Table 2 shows the results of a rated voltage application test performed at a temperature of 105 ° C. for 2000 hours for each of 20 pieces of 70 μF). Product aging is at 450V for 4 hours.

As is clear from Table 1, the electrolytes of Examples 1 to 23 of the present invention have the feature that the spark generation voltage is higher than those of the electrolytes of Conventional Examples 2 and 3, and therefore the products shown in Table 2 In the tests, the conventional examples 2 and 3 show a short circuit during aging, but the examples 1, 16 and 21 show no electrolytic solution during aging and no short circuit during the test, and have extremely excellent short-circuit resistance. It can be seen that it is. It should be noted that a highly reliable electrolytic capacitor can be obtained with little change in any of the characteristics such as the rate of change in capacitance, the change in tan δ, and the change in appearance.

FIG. 1 shows the formation and discharge characteristics of the present invention and the conventional electrolytic solution for driving an electrolytic capacitor at the time of constant current formation. In this comparison, the present invention is also superior. it is obvious.

Advantages of the Invention As is apparent from the above description of the embodiment, according to the present invention, it is possible to obtain an electrolytic solution for driving an electrolytic capacitor for medium and high pressures with a high spark generation voltage.

In addition, since γ-butyrolactone can be used as the main solvent, it is possible to provide an extremely reliable medium-to-high pressure electrolytic capacitor with little change in characteristics.

[Brief description of the drawings]

FIG. 1 is a characteristic diagram showing a comparison of formation / discharge characteristics during constant current formation between an electrolytic solution for driving an electrolytic capacitor according to an embodiment of the present invention and an electrolytic solution for driving an electrolytic capacitor according to a conventional example.

──────────────────────────────────────────────────の Continued on the front page (72) Inventor Keiji Mori 1006 Kazuma Kadoma, Osaka Prefecture Matsushita Electric Industrial Co., Ltd. (56) References JP-A-62-254416 (JP, A) JP-A-57-27013 (JP, A) (58) Fields investigated (Int. Cl. ⁶ , DB name) H01G 9/035

Claims (9)

(57) [Claims] (1) a solvent mainly composed of γ-butyrolactone,
1-methyl-1,7-heptanedicarboxylic acid, 1,7-dimethyl-1,7-heptanedicarboxylic acid, 1,3-dimethyl-1,3,
9-nonanetricarboxylic acid, 1,3-dimethyl-3-carbomethoxy-1,9-nonanedicarboxylic acid, 1,3-dimethyl-
1,7-heptanedicarboxylic acid, 1-methyl-3-ethyl-1,7-heptanedicarboxylic acid, 7-ethyl-1,16-hexadecanedicarboxylic acid, 7,8,11,12-tetramethyl-
1,18-octadecanedicarboxylic acid, 7,8-dimethyl-1,1
4-tetradecanedicarboxylic acid, 1-methyl-1,6-hexanedicarboxylic acid, 1,3-dimethyl-3-carbomethoxy-1,8-octanedicarboxylic acid, 1,3-dimethyl-1,3,
8-octanetricarboxylic acid, 1-methyl-1,8-octanedicarboxylic acid, 1,3-dimethyl-3-carbomethoxy-1,10-decanedicarboxylic acid, 1,3-dimethyl-1,3,10
An acid selected from -decanetricarboxylic acid, 7-phenyl-7-methoxy-1-octanecarboxylic acid, 6-phenyl-6-methoxy-heptanecarboxylic acid, 6-ethyl-1,14-tetradecanedicarboxylic acid, or An electrolytic solution for driving an electrolytic capacitor in which one or more of the salts are dissolved as a main solute. 2. The electrolytic solution for driving an electrolytic capacitor according to claim 1, wherein the salt is an ammonium salt. 3. The electrolytic solution for driving an electrolytic capacitor according to claim 1, wherein the salt is a secondary amine salt. 4. The electrolytic solution for driving an electrolytic capacitor according to claim 1, wherein the salt is a tertiary amine salt. 5. The electrolytic solution for driving an electrolytic capacitor according to claim 1, wherein the salt is a quaternary ammonium salt. 6. The electrolytic solution for driving an electrolytic capacitor according to claim 3, wherein the substituent of the secondary amine salt is one or two selected from a methyl group, an ethyl group, a propyl group, and a butyl group. 7. The electrolytic solution for driving an electrolytic capacitor according to claim 4, wherein the substituent of the tertiary amine salt is one or more selected from a methyl group, an ethyl group, a propyl group and a butyl group. 8. The electrolytic solution for driving an electrolytic capacitor according to claim 5, wherein the substituent of the quaternary ammonium salt is one or more selected from a methyl group, an ethyl group, a propyl group and a butyl group. 9. The electrolytic solution for driving an electrolytic capacitor according to claim 1, wherein ethylene glycol is used as a solvent to be mixed with γ-butyrolactone.