JPH0353768B2 - - Google Patents

Info

Publication number: JPH0353768B2
Authority: JP; Japan
Prior art keywords: tetraalkylammonium; electrolytic; salt; tetramethylammonium; hydroxide
Prior art date: 1986-11-07
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.): Expired

Application number

JP26406086A

Other languages

English (en)

Japanese (ja)

Other versions

JPS63119214A (ja

Priority date (The priority date 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 date listed.)

1986-11-07

Filing date

1986-11-07

Publication date

1991-08-16

1986-11-07 Application filed filed Critical

1986-11-07 Priority to JP26406086A priority Critical patent/JPS63119214A/ja

1988-05-23 Publication of JPS63119214A publication Critical patent/JPS63119214A/ja

1991-08-16 Publication of JPH0353768B2 publication Critical patent/JPH0353768B2/ja

Status Granted legal-status Critical Current

Links

239000003990 capacitor Substances 0.000 claims description 14
239000003792 electrolyte Substances 0.000 claims description 8
239000008151 electrolyte solution Substances 0.000 claims description 8
150000005621 tetraalkylammonium salts Chemical class 0.000 claims description 8
239000012528 membrane Substances 0.000 claims description 5
125000005207 tetraalkylammonium group Chemical group 0.000 claims description 5
238000005341 cation exchange Methods 0.000 claims description 4
238000006243 chemical reaction Methods 0.000 claims description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
150000002989 phenols Chemical class 0.000 claims description 3
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
150000001875 compounds Chemical class 0.000 claims description 2
150000007524 organic acids Chemical class 0.000 claims description 2
235000005985 organic acids Nutrition 0.000 claims description 2
150000003839 salts Chemical group 0.000 claims description 2
238000000034 method Methods 0.000 description 9
229910052736 halogen Inorganic materials 0.000 description 7
150000002367 halogens Chemical group 0.000 description 7
239000007864 aqueous solution Substances 0.000 description 6
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 6
238000005260 corrosion Methods 0.000 description 4
230000007797 corrosion Effects 0.000 description 4
-1 phenols Chemical class 0.000 description 4
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
RJXMRBDKMJQPTH-UHFFFAOYSA-M tetramethylazanium;phenoxide Chemical compound C[N+](C)(C)C.[O-]C1=CC=CC=C1 RJXMRBDKMJQPTH-UHFFFAOYSA-M 0.000 description 4
WDJHALXBUFZDSR-UHFFFAOYSA-N Acetoacetic acid Natural products CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 3
239000001715 Ammonium malate Substances 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
235000019292 ammonium malate Nutrition 0.000 description 3
150000001450 anions Chemical class 0.000 description 3
WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 description 3
IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 3
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
239000011976 maleic acid Substances 0.000 description 3
235000019260 propionic acid Nutrition 0.000 description 3
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
238000001953 recrystallisation Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical compound CC[N+](C)(CC)CC SEACXNRNJAXIBM-UHFFFAOYSA-N 0.000 description 3
HSNJERRVXUNQLS-UHFFFAOYSA-N 1-(4-tert-butylphenyl)propan-2-one Chemical compound CC(=O)CC1=CC=C(C(C)(C)C)C=C1 HSNJERRVXUNQLS-UHFFFAOYSA-N 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
238000005349 anion exchange Methods 0.000 description 2
230000006378 damage Effects 0.000 description 2
KVFVBPYVNUCWJX-UHFFFAOYSA-M ethyl(trimethyl)azanium;hydroxide Chemical compound [OH-].CC[N+](C)(C)C KVFVBPYVNUCWJX-UHFFFAOYSA-M 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
KTDMLSMSWDJKGA-UHFFFAOYSA-M methyl(tripropyl)azanium;hydroxide Chemical compound [OH-].CCC[N+](C)(CCC)CCC KTDMLSMSWDJKGA-UHFFFAOYSA-M 0.000 description 2
TYGMXGLQEONTHA-UHFFFAOYSA-M methyl(tripropyl)azanium;propanoate Chemical compound CCC([O-])=O.CCC[N+](C)(CCC)CCC TYGMXGLQEONTHA-UHFFFAOYSA-M 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000002994 raw material Substances 0.000 description 2
238000007789 sealing Methods 0.000 description 2
NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
229920000557 Nafion® Polymers 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
229910001413 alkali metal ion Inorganic materials 0.000 description 1
125000005210 alkyl ammonium group Chemical group 0.000 description 1
239000003957 anion exchange resin Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000011109 contamination Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000005868 electrolysis reaction Methods 0.000 description 1
235000019441 ethanol Nutrition 0.000 description 1
GOALBGSIDOWJHL-UHFFFAOYSA-L ethyl(trimethyl)azanium;carbonate Chemical compound [O-]C([O-])=O.CC[N+](C)(C)C.CC[N+](C)(C)C GOALBGSIDOWJHL-UHFFFAOYSA-L 0.000 description 1
UXYBXUYUKHUNOM-UHFFFAOYSA-M ethyl(trimethyl)azanium;chloride Chemical compound [Cl-].CC[N+](C)(C)C UXYBXUYUKHUNOM-UHFFFAOYSA-M 0.000 description 1
238000001914 filtration Methods 0.000 description 1
238000007429 general method Methods 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
239000010439 graphite Substances 0.000 description 1
229910052811 halogen oxide Inorganic materials 0.000 description 1
239000012535 impurity Substances 0.000 description 1
DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
229910001923 silver oxide Inorganic materials 0.000 description 1
229910001415 sodium ion Inorganic materials 0.000 description 1
239000000243 solution Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
WJZPIORVERXPPR-UHFFFAOYSA-L tetramethylazanium;carbonate Chemical compound [O-]C([O-])=O.C[N+](C)(C)C.C[N+](C)(C)C WJZPIORVERXPPR-UHFFFAOYSA-L 0.000 description 1
IPILPUZVTYHGIL-UHFFFAOYSA-M tributyl(methyl)azanium;chloride Chemical compound [Cl-].CCCC[N+](C)(CCCC)CCCC IPILPUZVTYHGIL-UHFFFAOYSA-M 0.000 description 1
YYDDABGTOBAXAR-UHFFFAOYSA-L triethyl(methyl)azanium;carbonate Chemical compound [O-]C([O-])=O.CC[N+](C)(CC)CC.CC[N+](C)(CC)CC YYDDABGTOBAXAR-UHFFFAOYSA-L 0.000 description 1
NIUZJTWSUGSWJI-UHFFFAOYSA-M triethyl(methyl)azanium;chloride Chemical compound [Cl-].CC[N+](C)(CC)CC NIUZJTWSUGSWJI-UHFFFAOYSA-M 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1

Landscapes

Oscillators With Electromechanical Resonators (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP26406086A 1986-11-07 1986-11-07 電解コンデンサ用電解液 Granted JPS63119214A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP26406086A JPS63119214A (ja)	1986-11-07	1986-11-07	電解コンデンサ用電解液

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP26406086A JPS63119214A (ja)	1986-11-07	1986-11-07	電解コンデンサ用電解液

Publications (2)

Publication Number	Publication Date
JPS63119214A JPS63119214A (ja)	1988-05-23
JPH0353768B2 true JPH0353768B2 (fr)	1991-08-16

Family

ID=17397975

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP26406086A Granted JPS63119214A (ja)	1986-11-07	1986-11-07	電解コンデンサ用電解液

Country Status (1)

Country	Link
JP (1)	JPS63119214A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4892944A (en) *	1987-05-13	1990-01-09	Mitsubishi Petrochemical Co., Ltd.	Process for producing quaternary salts

1986
- 1986-11-07 JP JP26406086A patent/JPS63119214A/ja active Granted

Also Published As

Publication number	Publication date
JPS63119214A (ja)	1988-05-23

Publication	Publication Date	Title
US4714530A (en)	1987-12-22	Method for producing high purity quaternary ammonium hydroxides
CA1335973C (fr)	1995-06-20	Methode de preparation d'hydroxydes d'ammonium quaternaire
US4572769A (en)	1986-02-25	Method of manufacturing tetramethyl ammonium hydroxide
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JPH0353768B2 (fr)	1991-08-16
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