JPH03225908A - Electrolyte for electrolytic capacitor - Google Patents
Electrolyte for electrolytic capacitorInfo
- Publication number
- JPH03225908A JPH03225908A JP2020636A JP2063690A JPH03225908A JP H03225908 A JPH03225908 A JP H03225908A JP 2020636 A JP2020636 A JP 2020636A JP 2063690 A JP2063690 A JP 2063690A JP H03225908 A JPH03225908 A JP H03225908A
- Authority
- JP
- Japan
- Prior art keywords
- phosphate
- acid
- electrolytic capacitor
- decandicarbonic
- guanylurea
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003990 capacitor Substances 0.000 title claims abstract description 17
- 239000003792 electrolyte Substances 0.000 title abstract description 4
- LWFBRHSTNWMMGN-UHFFFAOYSA-N 4-phenylpyrrolidin-1-ium-2-carboxylic acid;chloride Chemical compound Cl.C1NC(C(=O)O)CC1C1=CC=CC=C1 LWFBRHSTNWMMGN-UHFFFAOYSA-N 0.000 claims abstract description 8
- CEDDGDWODCGBFQ-UHFFFAOYSA-N carbamimidoylazanium;hydron;phosphate Chemical compound NC(N)=N.OP(O)(O)=O CEDDGDWODCGBFQ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims abstract description 4
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 4
- 239000008151 electrolyte solution Substances 0.000 claims description 11
- OWCLRJQYKBAMOL-UHFFFAOYSA-N 2-butyloctanedioic acid Chemical compound CCCCC(C(O)=O)CCCCCC(O)=O OWCLRJQYKBAMOL-UHFFFAOYSA-N 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000654 additive Substances 0.000 abstract description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052782 aluminium Inorganic materials 0.000 abstract description 3
- 230000006866 deterioration Effects 0.000 abstract description 3
- 239000011888 foil Substances 0.000 abstract description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract description 2
- 239000002253 acid Substances 0.000 abstract 3
- 230000000996 additive effect Effects 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- -1 for example Chemical compound 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
【発明の詳細な説明】
(従来の技術)
本発明は高温度で使用できる電解コンデンサ用電解液に
関する。DETAILED DESCRIPTION OF THE INVENTION (Prior Art) The present invention relates to an electrolytic solution for electrolytic capacitors that can be used at high temperatures.
(従来の技術)
電解コンデンサ用電解液は、高温度領域においても使用
できるように、例えば比較的分子量の大き2い有機酸あ
るいはその塩を溶質としている。有機酸系の溶質として
は特公昭60−13293号(1)
の通り1.6−デカンジカルボン酸が公知である。(Prior Art) An electrolytic solution for an electrolytic capacitor uses, for example, an organic acid with a relatively large molecular weight or a salt thereof as a solute so that it can be used even in a high temperature range. As an organic acid solute, 1,6-decanedicarboxylic acid is known as disclosed in Japanese Patent Publication No. 13293/1983 (1).
(発明が解決しようとする課題)
しかし、1.6−デカンジカルボン酸を溶質とする電解
液は、1.6−デカンジカルボン酸がコンデンサ素子を
形成するアルミ箔と反応して錯体を形成するために、コ
ンデンサの初期静電容量値が低く、高温負荷試験や高温
無負荷試験において静電容量が極端に減少し、漏れ電流
が増大する欠点がある。(Problem to be solved by the invention) However, in an electrolytic solution containing 1,6-decanedicarboxylic acid as a solute, 1,6-decanedicarboxylic acid reacts with the aluminum foil forming the capacitor element to form a complex. Another drawback is that the initial capacitance value of the capacitor is low, and the capacitance decreases dramatically during high-temperature load tests and high-temperature no-load tests, and leakage current increases.
これ等の欠点を改良するために、1.6−デカンジカル
ボン酸に、例えばリン酸や硫酸(特開昭58−9220
6号)、マレイン酸(特開昭5892208号)、クエ
ン酸(特開昭59−219920号)等を添加している
。In order to improve these drawbacks, 1,6-decanedicarboxylic acid, for example, phosphoric acid or sulfuric acid (Japanese Patent Application Laid-Open No. 58-9220
6), maleic acid (Japanese Unexamined Patent Publication No. 5892208), citric acid (Japanese Unexamined Patent Publication No. 59-219920), etc.
しかし、これ等の添加剤は熱的な安定性が低く、高温領
域の特性の改善の効果が低い。However, these additives have low thermal stability and are less effective in improving properties in high temperature regions.
本発明は、以上の欠点を改良し、高温領域において安定
で、電解コンデンサの特性を向上しうる電解コンデンサ
用電解液を提供することを目的とする。SUMMARY OF THE INVENTION An object of the present invention is to provide an electrolytic solution for electrolytic capacitors that improves the above-mentioned drawbacks, is stable in high-temperature ranges, and can improve the characteristics of electrolytic capacitors.
(2)
(課題を解決するための手段)
本発明は、上記の目的を達成するために、多価アルコー
ル類を主成分とする溶媒に、1.6−デカンジカルボン
酸またはその塩を溶解した電解コンデンサ用電解液にお
いて、リン酸グアニジンまたはリン酸グアニル尿素の少
なくとも一種類を溶解した電解コンデンサ用電解液を提
供するものである。(2) (Means for Solving the Problem) In order to achieve the above object, the present invention provides a solution in which 1,6-decanedicarboxylic acid or a salt thereof is dissolved in a solvent containing polyhydric alcohol as a main component. The present invention provides an electrolytic solution for electrolytic capacitors in which at least one of guanidine phosphate and guanylurea phosphate is dissolved.
(作用)
リン酸グアニジンやリン酸グアニル尿素は1゜6−デカ
ンジカルボン酸とアルミニウム箔とが反応して錯体を形
成するのを防止できる。そのために錯体を原因としてコ
ンデンサの初期静電容量値が低くなり、高温度領域にお
いて劣化する等を抑制できる。(Function) Guanidine phosphate and guanylurea phosphate can prevent 1°6-decanedicarboxylic acid and aluminum foil from reacting to form a complex. Therefore, the initial capacitance value of the capacitor becomes low due to the complex, and deterioration in a high temperature region can be suppressed.
(実施例) 以下、本発明を実施例に基づいて説明する。(Example) Hereinafter, the present invention will be explained based on examples.
溶媒には、■チレングリコールやジエチレングリコール
等の多価アルコールを用いる。As a solvent, use polyhydric alcohol such as ethylene glycol or diethylene glycol.
溶質には、1.6−デカンジカルボン酸や1゜(3) 6−デカンジカルボン酸アンモニウムを用いる。Solutes include 1,6-decanedicarboxylic acid and 1°(3) Ammonium 6-decanedicarboxylate is used.
そして、添加剤としては、特に、リン酸グアニジンやリ
ン酸グアニル尿素を用い、0.01〜5wt%添加する
。In particular, guanidine phosphate and guanylurea phosphate are used as additives, and are added in an amount of 0.01 to 5 wt%.
他に、PH調整剤としてアンモニア水を、化成性を改良
するために硼酸等を添加する。In addition, aqueous ammonia is added as a pH adjuster, and boric acid and the like are added to improve chemical conversion properties.
次に、本発明の実施例と従来の電解液について、比抵抗
と火花電圧を測定したところ表1の通りの結果が得られ
た。測定時の電解液の温度は、比抵抗が30℃、火花電
圧の場合が85°Cとする。Next, when the specific resistance and spark voltage were measured for the electrolytic solution of the example of the present invention and the conventional electrolyte, the results shown in Table 1 were obtained. The temperature of the electrolytic solution during measurement is 30°C for specific resistance and 85°C for spark voltage.
以下余白。Margin below.
(4)
表1
(5)
(6)
(7)
(8)
(9)
表1から明らかな通り、実施例1〜実施例10によれば
、比抵抗が460〜510Ω・cJ11火花電圧が42
5〜445■となる。そして従来例1〜従来例5は、比
抵抗が570〜600Ω・C11r N火花電圧が41
0〜430Vとなる。両者を比べると、実施例1〜実施
例10による方が従来例1〜従来例5よりも、比抵抗が
低く、約77%〜8(10)
9%となっている。(4) Table 1 (5) (6) (7) (8) (9) As is clear from Table 1, according to Examples 1 to 10, the specific resistance is 460 to 510Ω・cJ11 spark voltage is 42
5 to 445 ■. Conventional examples 1 to 5 have a specific resistance of 570 to 600Ω・C11rN spark voltage of 41
It becomes 0-430V. Comparing the two, Examples 1 to 10 have lower specific resistances than Conventional Examples 1 to 5, about 77% to 8(10)9%.
また、表1の組成の電解液のうち、実施例2、実施例4
〜実施例6、従来例1〜従来例3を含浸した定格400
V1100μFの電解コンデンサを各20個用いて、高
温負荷試験及び高温無負荷試験を行なった。高温負荷試
験条件は、温度105℃、印加電圧400■、放置時間
1000hrとする。また高温無負荷試験条件は、温度
105℃、放置時間1000hrとする。測定結果は表
2の通りとなる。Furthermore, among the electrolytes having the compositions shown in Table 1, Example 2 and Example 4
- Rating 400 impregnated with Example 6, Conventional Examples 1 to 3
A high-temperature load test and a high-temperature no-load test were conducted using 20 electrolytic capacitors each having a voltage of 1100 μF. The high temperature load test conditions are a temperature of 105° C., an applied voltage of 400 cm, and a standing time of 1000 hr. Further, the high temperature no-load test conditions are a temperature of 105° C. and a standing time of 1000 hr. The measurement results are shown in Table 2.
以下余白。Margin below.
(11)
(12)
表2から明らかな通り、初期の静電容量は実施例の電解
液を含浸したNOI〜NO4が105〜111μF、従
来例を含浸したNO5〜NO7が97.1〜98.3μ
Fとなり、前者の方が後者の約1.07〜1.14倍と
なっている。また、高温負荷試験後の特性について、静
電容量変化率は、N01〜NO4が−1,2〜−2,9
%、NO5〜NO7が−7,3〜−10,9となり、前
者は後者の約11%〜27%に抑えられる。tanδも
、初期値に比べて、NO1〜NO4が約1゜02〜1.
22倍、NO5〜NO7が約1.24〜1.45倍とな
り前者の方が劣化が少ない。そして漏れ電流は、NO1
〜NO4が5.1〜5゜9μA、N05〜N07が11
.0〜15.5μAとなり、前者の方が後者の約33%
〜54%に抑えられる。さらに、高温無負荷試験におい
て、静電容量変化率は、NO1〜NO4が−1,1〜−
2,3%、NO5〜NO7が−8,5〜−10゜5%と
なり、前者の方が後者の約10%〜27%となり、変化
が低い。tanδは初期値に比べて、(13)
NO1〜NO4が約0.98〜1.20倍、N。(11) (12) As is clear from Table 2, the initial capacitance was 105 to 111 μF for NOI to NO4 impregnated with the electrolytic solution of the example, and 97.1 to 98 μF for NO5 to NO7 impregnated with the conventional example. 3μ
F, and the former is about 1.07 to 1.14 times the latter. In addition, regarding the characteristics after the high temperature load test, the capacitance change rate is -1, 2 to -2, 9 for N01 to NO4.
%, NO5 to NO7 are -7.3 to -10.9, and the former is suppressed to about 11% to 27% of the latter. Tan δ is also about 1°02 to 1.0° for NO1 to NO4 compared to the initial value.
22 times, NO5 to NO7 about 1.24 to 1.45 times, and the former shows less deterioration. And the leakage current is NO1
~NO4 is 5.1~5゜9μA, N05~N07 is 11
.. 0 to 15.5 μA, the former being about 33% of the latter.
It can be suppressed to ~54%. Furthermore, in the high temperature no-load test, the capacitance change rate was -1 for NO1 to NO4, and 1 to -
2.3%, NO5 to NO7 is -8.5 to -10°5%, and the former is about 10% to 27% of the latter, and the change is low. Tan δ is approximately 0.98 to 1.20 times N for NO1 to NO4 (13) compared to the initial value.
5〜N07が約1.29〜1.59倍となり、前者の方
が低い。漏れ電流はNOI〜NO4が189〜211μ
A、NO5〜NO7が638〜710μAとなり、前者
は後者の約27%〜33%となる。5 to N07 is about 1.29 to 1.59 times, and the former is lower. Leakage current is 189 to 211 μ for NOI to NO4
A, NO5 to NO7 are 638 to 710 μA, and the former is about 27% to 33% of the latter.
(発明の効果)
以上の通り、本発明によれば、リン酸グアニジンやリン
酸グアニル尿素を添加することによって、電解コンデン
サに含浸した場合にその静電容量特性、tanδ特性、
漏れ電流特性を向上しうる電解コンデンサ用電解液が得
られる。(Effects of the Invention) As described above, according to the present invention, by adding guanidine phosphate or guanylurea phosphate, when impregnated into an electrolytic capacitor, the capacitance characteristics, tan δ characteristics,
An electrolytic solution for electrolytic capacitors that can improve leakage current characteristics is obtained.
Claims (1)
カンジカルボン酸またはその塩を溶解した電解コンデン
サ用電解液において、リン酸グアニジンまたはリン酸グ
アニル尿素の少なくとも一種類を溶解した電解コンデン
サ用電解液。(1) An electrolytic capacitor in which at least one type of guanidine phosphate or guanylurea phosphate is dissolved in an electrolytic solution for electrolytic capacitors in which 1,6-decanedicarboxylic acid or its salt is dissolved in a solvent mainly composed of polyhydric alcohol. electrolyte solution.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2020636A JPH03225908A (en) | 1990-01-31 | 1990-01-31 | Electrolyte for electrolytic capacitor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2020636A JPH03225908A (en) | 1990-01-31 | 1990-01-31 | Electrolyte for electrolytic capacitor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03225908A true JPH03225908A (en) | 1991-10-04 |
| JPH0557727B2 JPH0557727B2 (en) | 1993-08-24 |
Family
ID=12032718
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020636A Granted JPH03225908A (en) | 1990-01-31 | 1990-01-31 | Electrolyte for electrolytic capacitor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03225908A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0778731A (en) * | 1993-06-28 | 1995-03-20 | Sanken:Kk | High-conductivity composition for electrolyte |
| JP2007115947A (en) * | 2005-10-21 | 2007-05-10 | Nichicon Corp | Electrolyte for driving electrolytic capacitor |
| JPWO2023276589A1 (en) * | 2021-06-28 | 2023-01-05 |
-
1990
- 1990-01-31 JP JP2020636A patent/JPH03225908A/en active Granted
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0778731A (en) * | 1993-06-28 | 1995-03-20 | Sanken:Kk | High-conductivity composition for electrolyte |
| JP2007115947A (en) * | 2005-10-21 | 2007-05-10 | Nichicon Corp | Electrolyte for driving electrolytic capacitor |
| JPWO2023276589A1 (en) * | 2021-06-28 | 2023-01-05 | ||
| WO2023276589A1 (en) * | 2021-06-28 | 2023-01-05 | 三洋化成工業株式会社 | Electrolyte for electrolytic capacitor and electrolytic capacitor and hybrid electrolytic capacitor using said electrolyte |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0557727B2 (en) | 1993-08-24 |
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