CN101383227B - Electrolysis solution for electrolytic capacitors - Google Patents
Electrolysis solution for electrolytic capacitors Download PDFInfo
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- CN101383227B CN101383227B CN 200810169404 CN200810169404A CN101383227B CN 101383227 B CN101383227 B CN 101383227B CN 200810169404 CN200810169404 CN 200810169404 CN 200810169404 A CN200810169404 A CN 200810169404A CN 101383227 B CN101383227 B CN 101383227B
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Abstract
An electrolysis solution for electrolytic capacitors comprising an aqueous organic solvent consisting of water and a water-compatible organic solvent and 1,6-decanedicarboxylic acid or a salt thereof dissolved therein, which solution further contains one or more additives selected from the group consisting of dinitriles, pivalic acid and salts thereof, diesters, alkylated lactones, cyanoalkanoic esters, monocarboxylic acids each having a C3-7 alkyl chain and being substituted with two C1-4 alkyl groups at the beta -position to the carboxyl group and salts thereof, monocarboxylic acids each having a C3-7 alkyl chain and being substituted with one ethyl group at the alpha -position to the carboxyl group and salts thereof, and monocarboxylic acids derived from cyclic saturated compounds eachhaving five or six ring-constituting carbon atoms and salts thereof. When one or more compounds selected from among dinitriles, diesters, alkylated lactones and cyanoalkanoic esters are used as the additives, the 1,6-decanedicarboxylic acid may be replaced by other carboxylic acid.
Description
The application be that January 15, application number in 2002 are 02805883.6 the applying date, denomination of invention divides an application for the application of " electrolyte for electrolytic capacitor ".
Technical field
The present invention relates to electrolyte for electrolytic capacitor, that is, the driving electrolytic solution of electrolytic capacitor particularly relates to the electrolyte composition of the driving electrolytic solution that can be advantageously used for medium-high voltage aluminum electrolytic capacitor.
Background technology
In the past, as the driving electrolytic solution of mesohigh with aluminium electrolytic capacitor, can obtain higher sparking voltage (that is, using the proof voltage height), so the electrolyte that is dissolved in the water-containing organic solvent that is made of the ethylene glycol that contains low amounts of water as solute with boric acid or ammonium borate is employed widely.Yet, electrolyte for such composition, because conductivity is low, and because the esterification of ethylene glycol and boric acid generates a large amount of water, this moisture with react as the alumite of electrode, make this film deterioration, or under the high temperature more than 100 ℃, cause water evaporates, thereby press problems such as liter in taking place, therefore use at high temperature is difficult.
As the electrolyte that addresses the above problem, once propose to adopt organic dicarboxylic acid such as hexanedioic acid, decanedioic acid and azelaic acid or their salt to replace the electrolyte of boric acid or ammonium borate, they are also using in practice. still, because organic dicarboxylic acid is low for the solubility of water-containing organic solvent, so separate out crystallization at low temperatures easily, and because the problem of low-temperature characteristics deterioration of generation capacitor and so on, so use is had any problem at low temperatures.
Disclosed electrolyte for electrolytic capacitor is to add the butyl suberic acid (promptly in the special public clear 60-13293 communique, 1, the 6-decane dicarboxylic acid) or its salt as the electrolyte of solute. disclosedly in this communique contain 1, the electrolyte of 6-decane dicarboxylic acid or its salt, its aim is, improves sparking voltage and conductivity, and, solubility is also high, separates out problem so eliminated crystallization at low temperatures.
It is to add trimethylace tonitric (promptly that the spy opens in the clear 61-116815 communique disclosed electrolyte for electrolytic capacitor, neopentanoic acid) etc. uncle's monocarboxylic acid or its salt are as the electrolyte of solute. and disclosed aim is in this communique, by using uncle's monocarboxylic acid or its salt, realized the decline of the internal resistance of electrolytic capacitor, the rising of working voltage, the expansion of serviceability temperature scope.
The spy opens disclosed electrolyte for electrolytic capacitor in the clear 62-241322 communique, be with total carbon atom numbers such as isobutyric acid or trimethylace tonitric be 4～8 and side chain have the monoacid of alkyl or its salt as solute, be dissolved in the electrolyte of the excellent in temperature characteristic in the solution that contains ethylene glycol.
Disclosed electrolyte in the Te Kaiping 6-275472 communique, it is uncle's monocarboxylic acid and 2 with trimethylace tonitric and so on, the secondary dicarboxylic acids of 9-dimethyl decanedioic acid and so on combines, add the electrolyte that obtains in the solution that contains ethylene glycol to, the sparking voltage of this electrolyte and conductivity height, and it is good to change () one-tenth (film) property.
Disclosed electrolyte in the Te Kaiping 6-302475 communique, be uncle's monocarboxylic acid or its salt and 2 with trimethylace tonitric and so on, secondary dicarboxylic acids or its salt of 9-dimethyl decanedioic acid and so on combine, add the electrolyte of modulating in the solution that contains ethylene glycol to, the sparking voltage of this electrolyte and conductivity height, and it is good to change () one-tenth (film) property.
Yet, recently, adopt the various e-machines of rectifier power source in general family, to be extensive use of, so the requirement for the tight security of the electrolytic capacitor that is used for such e-machine is stronger. in order to improve the fail safe of electrolytic capacitor, then must improve the sparking voltage (use proof voltage) of electrolyte for electrolytic capacitor, but the voltage-resistent characteristic of hitherto known electrolytic capacitor can't be said so and can fully be satisfied.
Therefore, main purpose of the present invention is to provide a kind of electrolyte for electrolytic capacitor, this electrolyte is aspect conductivity and changing into property (form on the surface as the metal materials such as aluminium foil of electrolytic capacitor anode insulating properties oxide film thereon make the operability of dielectric good), reached the level that can fully meet the demands on practical, and the sparking voltage (use proof voltage) of gained level is compared with in the past electrolyte for electrolytic capacitor the time, demonstrates higher use proof voltage.
Summary of the invention
The present invention relates to a kind of electrolyte, it is characterized in that, this electrolyte is with 1,6-decane dicarboxylic acid or its salt are dissolved in and show by water with water and to constitute in the aqueous organic solvent that the organic solvent of intermiscibility constitutes, and, also contain and be selected from dinitrile compound, trimethylace tonitric or its salt, diester compound, lactone compound with alkyl, cyano group alkanoate compound, have the alkyl chain of 3～7 of carbon numbers and monocarboxylic acid or its salt of the alkyl of two carbon numbers 1～4 are arranged in the β position of carboxyl, have the alkyl chain of 3～7 of carbon numbers and monocarboxylic acid or its salt of an ethyl are arranged in the α position of carboxyl, and to become the ring carbon atom number be 5 or 6 ring-type saturated compounds monocarboxylic acid or more than one the adding ingredient in its salt.
The invention still further relates to a kind of electrolyte, it is characterized in that, this electrolyte is carboxylic acid or its salt to be dissolved in show in the aqueous organic solvent that the organic solvent of intermiscibility constitutes by water with water and to constitute, and, also contain and be selected from dinitrile compound, diester compound, have the lactone compound of alkyl and more than one the adding ingredient in the cyano group alkanoate compound.
The invention still further relates to a kind of electrolytic capacitor, this electrolytic capacitor is in closed container, contain the metal material that forms oxide-film from the teeth outwards and the electrolytic capacitor of electrolyte, it is characterized in that, as electrolyte, use above-mentioned any electrolyte. can preferably use aluminium foil as metal material.
Use the electrolytic capacitor of electrolyte of the present invention, compare with electrolytic capacitor of the same race in the past, demonstrate the changing into property and the conductance of par, on the other hand, its sparking voltage (proof voltage) is up to more than the 470V, and the selection and the combination of the adding ingredient by changing electrolyte, can reach more than the 480V, also can reach more than the 490V, also can also reach the above sparking voltage of 500V.
The embodiment of invention
Electrolyte of the present invention is characterized in that, is showing in the aqueous organic solvent that the organic solvent of intermiscibility constitutes dissolving as 1 of the 1st adding ingredient by water with water, 6-decane dicarboxylic acid or its salt, but also dissolve one or more the 2nd adding ingredients.
At first, for as the organic solvent of electrolyte of the present invention, and show that with water the organic solvent of intermiscibility describes. the electrolyte of electrolytic capacitor, in the past, be to use by water with water always and show that aqueous organic solvent (water-containing organic solvent) that the organic solvent of intermiscibility constitutes is as solvent, and show the organic solvent of intermiscibility with water as what use among the present invention, can use well-known various organic solvents in this purposes. as such organic solvent, can enumerate, the alcohols of polyalcohols or unary alcohol etc., the diester class, cyano group alkanoate class, lactone, the sulfoxide class of dimethyl sulfoxide (DMSO) and so on is preferred. and, organic solvent, it also can be the mixture of two or more organic solvent, so long as show with water and also can mix the organic solvent of intermiscibility with the organic solvent that in water, does not show intermiscibility.
As polyalcohols, can enumerate, ethylene glycol, diethylene glycol (DEG), propylene glycol, DPG, 1, ammediol, 1,2-butanediol, 1,3-butanediol, 2,3-butanediol, 1,5-pentanediol, 2-methyl isophthalic acid, ammediol, 2,2-dimethyl-1, ammediol, tetramethylenthanediol, 2-methyl-2,4-pentanediol, 2-ethyl-1,3-hexylene glycol, 3-methyl isophthalic acid, 5-pentanediol, glycerol, 1,2,4-butantriol, trimethylolethane, sweet mellow wine, D-sorbite, galactitol, polyvinyl alcohol etc.
As unary alcohol, can enumerate 2-methyl cellosolve, cellosolvo, 2-propoxyl group ethanol, 2-isopropoxide ethanol, butoxy ethanol, 3-methyl-3-methoxyl group-1-butanols, 3-methoxyl group-1-butanols, 1-methoxyl group-2-propyl alcohol, 1-ethyoxyl-2-propyl alcohol, 1-methoxyl group-2-butanols etc.
As lactone, can enumerate gamma-butyrolacton, δ-Wu Neizhi, ε-caprolactone etc.
Particularly preferably be the mixture of ethylene glycol and ethylene glycol and lactone.
Water content in the water-containing organic solvent, as amount with respect to whole electrolyte, normally below the 5 weight %, preferably 0.1 weight % above, below the 4 weight %.
The first adding ingredient person as electrolyte of the present invention, be 1,6-decane dicarboxylic acid or its salt are (for example, salt with organic bases such as ammonium salt, methyl amine salt, dimethyl amine salt, trismethylamine salt, ethyl amine salt, diethyl amine salt, triethyl amine salt, quaternary ammonium salts). and, the preferable range of the pH of electrolyte of the present invention is 5～7, in particular for reaching about 6, preferably with 1,6-decane dicarboxylic acid or its salt, use combines after the ratio of adjusting them, or with 1, the 6-decane dicarboxylic acid is made salify separately and is used.
In addition, research by the inventor is confirmed, common available 1, be mixed with from 1 of its manufacture method in 6-decane dicarboxylic acid or its salt, 10-decane dicarboxylic acid and/or its salt is as impurity .1, the 10-decane dicarboxylic acid, its fusing point is than higher, be 130 ℃ (1, the fusing point of 6-decane dicarboxylic acid is 65 ℃), so it contains sometimes in a large number as impurity, separate out easily at low temperatures, capacitor specific characteristics under the low temperature is descended, in addition, cause easily with electrolyte in the glycol ester exchange, thereby make the capacitor specific characteristics deteriorations such as conductivity generation deterioration under the high temperature easily. therefore, 1,1 in 6-decane dicarboxylic acid or its salt, the mixing amount of 10-decane dicarboxylic acid and/or its salt, with respect to 1, the weight of 6-decane dicarboxylic acid or its salt preferably becomes below the 3 weight %, more preferably below the 1 weight %.
And, commercially available 1, in 6-decane dicarboxylic acid or its salt as impurity contain 1,10-decane dicarboxylic acid and/or its salt, in refining step, be difficult to be removed fully, when making with extra care according to common crystallization, 1, mix in 6-decane dicarboxylic acid or its salt and have 1 about 5～8 weight %, 10-decane dicarboxylic acid and/or its salt.
As reducing 1, in 6-decane dicarboxylic acid or its salt as impurity contain 1, the method for the combined amount of 10-decane dicarboxylic acid and/or its salt is preferably carried out process for purification as described below.
Will be as 1, impurity contains in the 6-decane dicarboxylic acid 1, after the esterification of 10-decane dicarboxylic acid, by separated 1,6-decane dicarboxylic acid ester, it remains untouched and directly is hydrolyzed, remake into carboxylic acid method (below, be called the way of distillation) be preferred. distillation condition, preferred reflux ratio 0.01～100. more preferably 0.1～30. theoretical cam curve are preferred 2～90, and more preferably 5～50.For distillation, get final product decompression distillation, also but there is no particular limitation in air-distillation, but preferably under 0.1～200mm Hg, particularly preferably in distilling under 0.5～30mm Hg. the kind of ester has no particular limits, but can enumerate, the propyl ester of methyl esters, ethyl ester, straight or branched, the butyl ester of straight or branched etc. and the advantage of this distillating method is, can remove the butyric acid of the carboxylic acid of the low-molecular-weight (low boiling) that usually contains as impurity in the 6-decane dicarboxylic acid or acid etc. simultaneously 1.
In the electrolyte 1, the content of 6-decane dicarboxylic acid or its salt, for obtaining good electrical conductivity and proof voltage, preferred range is 0.1～50 weight %.In order to obtain better characteristic, amount that can preferred 1～40 weight % scope particularly preferably is the amount of 1～20 weight % (wherein, 1～15 weight % also has 3～10 weight %) scope.
In addition, as second adding ingredient of the present invention, when using dinitrile compound, diester compound, lactone compound or cyano group alkanoate compound with alkyl, as first adding ingredient, can use as the known carboxylic acid of the adding ingredient of electrolyte for electrolytic capacitor or its salt and replace 1,6-decane dicarboxylic acid or its salt. can use following carboxylic acid or its salt as such carboxylic acid or its salt.
5, the 6-decane dicarboxylic acid, decanedioic acid, adipic acid, 3-lauryl hexanedioic acid, 2, the 9-decanedioic acid, azelaic acid, 1,7-octane dicarboxylic acids, benzoic acid, 3, the 3-acid dimethyl, 2,2-diisopropyl propionic acid, the 2-methyl nonanoic acid, 2,4-dimethyl-4-methoxycarbonyl 11 (carbon) docosandioic acid, 2,4,6-trimethyl-4,6-dimethoxy carbonyl 13 (carbon) docosandioic acid, 8,9-dimethyl-8,9-dimethoxy carbonyl 16 (carbon) docosandioic acid, 11-cyano group 11 (carbon) alkanoic acid, 7-cyano group 11 (carbon) alkanoic acid, 2-butyl-7-cyano group enanthic acid, the ammonium salt of these carboxylic acids, the methyl amine salt, the dimethyl amine salt, trismethylamine salt, the ethyl amine salt, the diethyl amine salt, triethyl amine salt, the salt of quaternary ammonium salt etc. and organic base.
The content of these carboxylic acids or its salt in the electrolyte, for obtaining good electrical conductivity and proof voltage, preferred range is that 0.1～50 weight %. is in order to obtain better characteristic, amount that can preferred 1～40 weight % scope, particularly preferably be 1～20 weight % (wherein, 1～15 weight %) amount of scope.
In the electrolyte of the present invention, adding as second adding ingredient, is in the following adding ingredient any, and these adding ingredients can dissolve one or more in electrolyte.
Dinitrile compound, trimethylace tonitric or its salt, diester compound, the lactone compound with alkyl, cyano group alkanoate compound, have the alkyl chain of 3～7 of carbon numbers and have in the β position of carboxyl the alkyl of two carbon numbers 1～4 monocarboxylic acid or its salt, have the alkyl chain of 3～7 of carbon numbers and the monocarboxylic acid of an ethyl arranged or its salt and to become the ring carbon atom number be 5 or 6 ring-type saturated compounds monocarboxylic acid or its salt in the α position of carboxyl.
Below, these second adding ingredients are described in detail.
[dinitrile compound]
As dinitrile compound, preferably on the alkylidene chain of 1～12 of carbon number with the dinitrile compound of two cyano group. alkylidene chain, it can be the straight chain shape, prop up any of chain. as the concrete example of dinitrile compound, can enumerate as the straight chain dinitrile compound, succinonitrile, glutaronitrile, adiponitrile, 1,5-dicyano pentane, 1,6-dicyano hexane, 1,7-dicyano heptane, 1,8-dicyano octane, 1,9-dicyano nonane, 1,10-dicyano decane, 1,12-dicyano 12 (carbon) alkane. as dividing dendritic dinitrile compound to enumerate, the tetramethyl succinonitrile, the 2-methyl cellosolve acetate glutaronitrile, 2,4-dimethyl-penten dintrile, 2,2,4,4-tetramethyl glutaronitrile, 1,4-dicyano pentane, 2,5-dimethyl-2,5-hexane dintrile, 2,6-dicyano heptane, 2,7-dicyano octane, 2,8 dicyano nonanes, 1,6-dicyano decane.Particularly preferably be adiponitrile.
The tret (content) of nitrile compound in electrolyte, with respect to the total amount of electrolyte, common scope is the preferably scope of 1～40 weight % of 0.1～50 weight %., particularly preferably is 1～20 weight %.
[trimethylace tonitric or its salt]
Trimethylace tonitric also is called pivalic, is with (CH
3)
3The compound of COOH chemical formulation. as its salt (pivalate), can enumerate the salt of trimethylace tonitric and above-mentioned organic base.
The trimethylace tonitric of electrolyte or the content of its salt, with respect to the total amount of electrolyte, the amount of preferred 1～20 weight % scope of trimethylace tonitric or its salt particularly preferably is the amount of 3～15 weight % scopes.
In addition, as with respect to first adding ingredient 1, the amount of 6-decane dicarboxylic acid or its salt, with trimethylace tonitric or its salt: 1, the weight ratio that 6-decane dicarboxylic acid or its salt are represented preferably becomes the amount of 25:75～90:10 scope. in addition, as trimethylace tonitric or its salt and 1, the total amount of 6-decane dicarboxylic acid or its salt, the scope of 2～30 weight % of electrolyte total amount preferably particularly preferably is the scope of 6～25 weight %.
In addition, trimethylace tonitric or its salt, it is preferred being contained in the electrolyte with above-mentioned nitrile compound.
[diester compound]
Diester compound, the diester compound that preferably has the alkylidene of carbon number 2～18 (particularly 4～12). alkylidene can be the straight chain shape also can be any of a chain. as the concrete example of diester compound, can enumerate the amber dimethyl succinate of straight chain shape, dimethyl glutarate, dimethyl adipate, Dimethyl 1,7-heptanedioate, the suberic acid dimethyl ester, dimethyl azelate, 1,9-decane dicarboxylic acid dimethyl ester, 1,10-decane dicarboxylic acid dimethyl ester. in addition, also can use the dendritic tetramethyl dimethyl succinate of branch, 2-methylglutaric acid dimethyl ester, 2,4-dimethylated pentanedioic acid dimethyl ester, 22,4,4-tetramethyl 4-dimethylated pentanedioic acid dimethyl ester, 1,6-decane dicarboxylic acid dimethyl ester etc. and, diester compound, be not limited to only have the methyl ester of methyl at two ends of these strands, and can be ethyl ester, propyl diester, phenylester. these diester compounds are with respect to the addition (content) of electrolyte total amount, the amount of 0.01～50 weight % scope normally. the scope of 0.1～40 weight % preferably particularly preferably is the amount of 1～20 weight %.
When in electrolyte, adding above-mentioned diester compound, preferably also contain trimethylace tonitric or its salt of 1～20 weight %.
[lactone compound] with alkyl
As lactone compound with alkyl, preferably have 1 above methyl, ethyl, propyl group, butyl, amyl group, carbon numbers such as base, heptyl, octyl group reach the lactone compound of 1～12 alkyl. alkyl also can be the alkyl of the band branch of isopropyl or isobutyl group and so on. in these lactone compounds, particularly preferably be, have the lactone compound that carbon number reaches 4～8 alkyl chain.
Concrete example as preferred lactone compound, can enumerate the nonyl lactone with a straight chain shape amyl group, γ-11 (carbon) lactone etc. with a straight chain shape heptyl. also can be delta-lactone compound or ε-lactone compound with alkyl. the content of lactone compound, with respect to the electrolyte total amount, 0.1～50 weight % normally, 1～20 weight % preferably particularly preferably is the amount of 1～10 weight % scope.
[cyano group alkanoate compound]
Cyano group alkanoate compound, the compound that preferably has the alkylidene of carbon number 2～18 (particularly 4～12). alkylidene can be the straight chain shape or divide dendritic any one. as the concrete example of cyano group alkanoate derivative, can enumerate the 3-cyanopropionic acid methyl esters of straight chain shape, 4-cyano butyric acid methyl esters, 5-cyanopentanoic acid methyl esters, the sour methyl esters of 6-cyano group, 7-cyano group enanthic acid dimethyl methyl esters, 8-cyano group methyl caprylate, 9-cyano group methyl pelargonate, 10-cyano group methyl caprate, the sour methyl esters of 11-cyano group 11 (carbon), 12-cyano group methyl laurate etc. in addition, can enumerate the dendritic sour methyl esters of 7-cyano group 11 (carbon) of branch, 2-butyl-7-cyano group methyl heptanoate etc. but be not limited to above-mentioned methyl ester, it also can be ethyl ester, propyl diester, phenylester. the content of cyano group alkanoate derivative, with respect to the electrolyte total amount, the amount of 0.01～50 weight % scope normally, 0.1～40 weight % preferably particularly preferably is the amount of 1～20 weight % scope.
[have the alkyl chain of 3～7 of carbon numbers and monocarboxylic acid or its salt of the alkyl of two carbon numbers 1～4 arranged in the β position of carboxyl]
This monocarboxylic acid is to use formula: (R
1) (R
2) (R
3) CH
2COOH[R
1, R
2, and R
3The alkyl of representing carbon number 1～4 respectively independently] expression compound.
The R of the monocarboxylic acid of representing with above-mentioned formula
1, R
2, R
3Expression independently respectively, the alkyl of carbon numbers 1～4 such as methyl, ethyl, n-pro-pyl, isopropyl, normal-butyl, sec-butyl, the tert-butyl group.Preferable methyl or ethyl.
The concrete example of the monocarboxylic acid of above-mentioned general formula can be enumerated, and 3,3-acid dimethyl (R
1=R
2=R
3=methyl), 3,3-dimethyl valeric acid (R
1=R
2=methyl, R
3=ethyl), 3,3-diethyl butyric acid (R
1=R
2=ethyl, R
3=methyl), 3,3-diethyl valeric acid (R
1=R
2=R
3=ethyl), 3,3,4-trimethyl valeric acid (R
1=R
2=methyl, R
3=isopropyl) etc.As the salt of above-mentioned monocarboxylic acid, can enumerate the salt of this monocarboxylic acid and above-mentioned organic base.
The content of above-mentioned monocarboxylic acid or its salt, with the electrolyte total amount as benchmark, 0.1～50 weight % normally, 1～40 weight % preferably particularly preferably is the amount of 1～20 weight % scope.
[have the alkyl chain of 3～7 of carbon numbers and monocarboxylic acid or its salt of an ethyl arranged in the α position of carboxyl]
As the concrete example of this monocarboxylic acid, can enumerate 2 Ethylbutanoic acid, 2-ethyl valeric acid, 2-ethyl acid and 2-ethyl enanthic acid etc.As the salt of these monocarboxylic acids, can enumerate the salt of this monocarboxylic acid and above-mentioned organic base.
The content of this monocarboxylic acid as benchmark, becomes the amount of 0.1～50 weight % scope with the electrolyte total amount usually, and 1～40 weight % preferably particularly preferably is the amount of 1～20 weight % scope.
[one-tenth ring carbon atom number is 5 or 6 ring-type saturated compounds monocarboxylic acid or its salt]
As the concrete example of this monocarboxylic acid, can enumerate pentamethylene dicarboxylic acids and cyclohexane dicarboxylic acid etc. as the salt of these monocarboxylic acids, can enumerate the salt of this monocarboxylic acid and above-mentioned organic base.
The content of this monocarboxylic acid as benchmark, becomes the amount of 0.1～50 weight % scope with the electrolyte total amount usually, and 1～40 weight % preferably particularly preferably is the amount of 1～20 weight % scope.
[adding ingredients of other that can add arbitrarily]
In the electrolyte that electrolytic capacitor of the present invention is used, in preferred interpolation acidic alkyl phosphoric acid ester, phosphoric acid, the phosphorous acid one or more, the hydration deterioration of the anodic oxide coating that takes place in the time of can suppressing the long preservation capacitor, the rising of the leakage current of all right suppression capacitor.The addition of acidic alkyl phosphoric acid ester, phosphoric acid or phosphorous acid as benchmark, is preferably the amount of 0.02～4 weight % scope with the electrolyte total amount.
Can also add have internal pressure rising function that the inner hydrogen that takes place of suppression capacitor causes, in the aromatic nitro compounds such as o-nitrophenol, m-nitrophenol, p-nitrophenol, m-nitro-acetophenone one or more. the addition of aromatic nitro compound, as benchmark, be preferably the amount of 0.02～6 weight % scope with the electrolyte total amount.
Below, enumerate embodiment and specifically describe the present invention. and, in the following embodiments, in the water-containing organic solvent that ethylene glycol (the perhaps composition of ethylene glycol and gamma-butyrolacton) and water constitute, the electrolyte of the adding ingredient that has dissolved one or more is added in modulation. then, aluminium foil is immersed in this electrolyte, and is determined at 10mA/cm
2Current density under when changing into constant current sparking voltage (V), reach conductivity under time of advent (changing into the time: divide) of voltage 400V and 20 ℃ (than conductivity: mS/cm). these measured values are put down in writing in the lump.
For the electrolyte of known representational cooperation, also implement same mensuration, these measured values are record in the lump also.
[comparative example 1]
1,6-decane dicarboxylic acid ammonium (15 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 430V, change into the time: 4.8 minutes, conductivity: 2.1mS/cm
[comparative example 2]
Trimethylace tonitric ammonium (15 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 440V, change into the time: 5.6 minutes, conductivity: 2.2mS/cm
[embodiment 1]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 475V, change into the time: 5.4 minutes, conductivity: 1.7mS/cm
[embodiment 2]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (52 weight %)
Adiponitrile (30 weight %)
Water (3 weight %)
Sparking voltage: 520V, change into the time: 5.6 minutes, conductivity: 1.6mS/cm
[embodiment 3]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (81 weight %)
Adiponitrile (1 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 5.2 minutes, conductivity: 1.7mS/cm
[embodiment 4]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (72 weight %)
Adiponitrile (10 weight %)
Water (3 weight %)
Sparking voltage: 510V, change into the time: 5.4 minutes, conductivity: 1.7mS/cm
[embodiment 5]
1,6-decane dicarboxylic acid ammonium (7.5 weight %)
Trimethylace tonitric ammonium (7.5 weight %)
Ethylene glycol (72 weight %)
Adiponitrile (10 weight %)
Water (3 weight %)
Sparking voltage: 495V, change into the time: 5.1 minutes, conductivity: 1.7mS/cm
[embodiment 6]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Trimethylace tonitric ammonium (5 weight %)
Ethylene glycol (72 weight %)
Adiponitrile (10 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 4.8 minutes, conductivity: 1.7mS/cm
[embodiment 7]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (60 weight %)
1,5-pentanediol (12 weight %)
Adiponitrile (10 weight %)
Water (3 weight %)
Sparking voltage: 500V, change into the time: 5.6 minutes, conductivity: 1.4mS/cm
[embodiment 8]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (60 weight %)
1,2,4-butantriol (12 weight %)
Adiponitrile (10 weight %)
Water (3 weight %)
Sparking voltage: 500V, change into the time: 5.4 minutes, conductivity: 1.3mS/cm
[embodiment 9]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (60 weight %)
1,2-butanediol (12 weight %)
1,6-dicyano decane (10 weight %)
Water (3 weight %)
Sparking voltage: 495V, change into the time: 5.5 minutes, conductivity: 1.5mS/cm
[embodiment 10]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (60 weight %)
Diethylene glycol (12 weight %)
1,6-dicyano decane (10 weight %)
Water (3 weight %)
Sparking voltage: 510V, change into the time: 5.4 minutes, conductivity: 1.3mS/cm
[embodiment 11]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (60 weight %)
Tetramethylenthanediol (12 weight %)
Own dicyan (10 weight %)
Water (3 weight %)
Sparking voltage: 515V, change into the time: 6.2 minutes, conductivity: 1.1mS/cm
[embodiment 12]
1,6-decane dicarboxylic acid ammonium (2.5 weight %)
Trimethylace tonitric ammonium (7.5 weight %)
Ethylene glycol (70 weight %)
Own dicyan (17 weight %)
Water (3 weight %)
Sparking voltage: 560V, change into the time: 6.1 minutes, conductivity: 0.8mS/cm
[embodiment 13]
1,6-decane dicarboxylic acid ammonium (2.5 weight %)
Trimethylace tonitric ammonium (7.5 weight %)
Ethylene glycol (22 weight %)
Gamma-butyrolacton (50 weight %)
Own dicyan (15 weight %)
Water (3 weight %)
Sparking voltage: 560V, change into the time: 6.0 minutes, conductivity: 0.9mS/cm
[embodiment 14]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Ethylene glycol (73 weight %)
Own dicyan (15 weight %)
Water (2 weight %)
Sparking voltage: 500V, change into the time: 4.6 minutes, conductivity: 1.4mS/cm
[embodiment 15]
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (73 weight %)
Own dicyan (15 weight %)
Water (2 weight %)
Sparking voltage: 510V, change into the time: 5.4 minutes, conductivity: 2.0mS/cm
Comparing embodiment 1～15 and comparative example 1～2 as a result the time as can be known, according to the present invention, by adding 1,6-decane dicarboxylic acid ammonium (or trimethylace tonitric ammonium) and nitrile compound be as the electrolyte of adding ingredient, and only adds 1, and the electrolyte of 6-decane dicarboxylic acid ammonium is compared, about the time of changing into and conductivity do not have big variation, but sparking voltage but obviously improves. in addition, about with 1, the electrolyte that 6-decane dicarboxylic acid ammonium adds the trimethylace tonitric ammonium together more also is same.
Secondly, shown embodiment also shows, as 1 of adding ingredient, 6-decane dicarboxylic acid ammonium uses 1 of common industrial products, and 6-decane dicarboxylic acid ammonium is (as impurity, contain 1 of 6 weight %, 10-decane dicarboxylic acid ammonium) time, and as high-purity 1,6-decane dicarboxylic acid ammonium (1, the mixing amount of 10-decane dicarboxylic acid ammonium: the difference between the performance of electrolyte 0.1 weight %). and, high-purity 1,1 of 6-decane dicarboxylic acid ammonium, 6-decane dicarboxylic acid ammonium, available following method obtains.
" high-purity 1, the method for making of 6-decane dicarboxylic acid "
To obtain as industrial products 1, the 6-decane dicarboxylic acid is (as impurity, contain 1 of 6 weight %, the 10-decane dicarboxylic acid) carry out esterification after, by in reflux ratio be 1, theoretical cam curve is to carry out rectifying under 20 the condition, from 1,6-decane dicarboxylic acid methyl esters (boiling point: 156 ℃/separate 1 in 10mmHg), 10-decane dicarboxylic acid methyl esters (boiling point: 165 ℃/10mmHg).Then, make 1, the hydrolysis of 6-decane dicarboxylic acid methyl esters obtains high-purity 1, and the 6-decane dicarboxylic acid (1, the mixing amount of 10-decane dicarboxylic acid: 0.1 weight %).
In addition, in the following embodiments, in the water-containing organic solvent that is made of ethylene glycol and water, the electrolyte of the adding ingredient that dissolves one or more is added in modulation, and aluminium foil is immersed in this electrolyte, and is determined at 10mA/cm
2Current density under when changing into constant current sparking voltage (V), reach the following conductivity of time of advent (changing into the time: divide) of voltage 400V and 20 ℃ (than conductivity: mS/cm). and measure again electrolyte at 105 ℃ of maintenance conductivity rates of descent (%) after 720 hours down. these measured values are also put down in writing in the lump.
[comparative example 3]
1,6-decane dicarboxylic acid ammonium is (industrial: 15 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 430V, change into the time: 4.8 minutes, conductivity: 2.1mS/cm
Conductivity rate of descent: 31%
[embodiment 16]
1,6-decane dicarboxylic acid ammonium is (industrial: 5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 475V, change into the time: 5.4 minutes, conductivity: 1.7mS/cm
Conductivity rate of descent: 18%
[embodiment 17]
1,6-decane dicarboxylic acid ammonium (high-purity: 5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 5.3 minutes, conductivity: 1.7mS/cm
Conductivity rate of descent: 17%
[embodiment 18]
1,6-decane dicarboxylic acid ammonium is (industrial: 7.5 weight %)
Trimethylace tonitric ammonium (7.5 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 5.0 minutes, conductivity: 1.8mS/cm
Conductivity rate of descent: 21%
[embodiment 19]
1,6-decane dicarboxylic acid ammonium (high-purity: 7.5 weight %)
Trimethylace tonitric ammonium (7.5 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 485V, change into the time: 4.9 minutes, conductivity: 1.8mS/cm
Conductivity rate of descent: 19%
[embodiment 20]
1,6-decane dicarboxylic acid ammonium is (industrial: 10 weight %)
Trimethylace tonitric ammonium (5 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 470V, change into the time: 4.7 minutes, conductivity: 1.7mS/cm
Conductivity rate of descent: 26%
[embodiment 21]
1,6-decane dicarboxylic acid ammonium (high-purity: 10 weight %)
Trimethylace tonitric ammonium (5 weight %)
Ethylene glycol (82 weight %)
Water (3 weight %)
Sparking voltage: 475V, change into the time: 4.6 minutes, conductivity: 1.8mS/cm
Conductivity rate of descent: 22%
[embodiment 22]
1,6-decane dicarboxylic acid ammonium (high-purity: 5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (70 weight %)
1,5-pentanediol (12 weight %)
Water (3 weight %)
Sparking voltage: 475V, change into the time: 5.3 minutes, conductivity: 1.4mS/cm
Conductivity rate of descent: 17%
[embodiment 23]
1,6-decane dicarboxylic acid ammonium (high-purity: 5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (70 weight %)
1,2,4-butantriol (12 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 4.8 minutes, conductivity: 1.3mS/cm
Conductivity rate of descent: 16%
[embodiment 24]
1,6-decane dicarboxylic acid ammonium (high-purity: 5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (70 weight %)
1,2-butanediol (12 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 5.2 minutes, conductivity: 1.5mS/cm
Conductivity rate of descent: 16%
[embodiment 25]
1,6-decane dicarboxylic acid ammonium (high-purity: 5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (70 weight %)
Diethylene glycol (12 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 4.7 minutes, conductivity: 1.5mS/cm
Conductivity rate of descent: 16%
[embodiment 26]
1,6-decane dicarboxylic acid ammonium (high-purity: 5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (70 weight %)
Tetramethylenthanediol (12 weight %)
Water (3 weight %)
Sparking voltage: 485V, change into the time: 5.9 minutes, conductivity: 1.1mS/cm
Conductivity rate of descent: 14%
From comparative example 3, with the result of embodiment 16～26 as can be known, as 1,6-decane dicarboxylic acid ammonium, by using highly purified 1,6-decane dicarboxylic acid ammonium (be common industrial products to be made with extra care make 1, the mixing amount of 10-decane dicarboxylic acid ammonium has reduced), can reach higher sparking voltage and conductivity rate of descent still less.
Below, in the water-containing organic solvent that is made of ethylene glycol and water, modulation is except 1, beyond the 6-decane dicarboxylic acid ammonium, also add the electrolyte of dissolving diester compound, lactone compound or cyano group alkanisation compound, and aluminium foil is immersed in this electrolyte, and be determined at 10mA/cm with alkyl
2Current density under when changing into constant current sparking voltage (V), reach the following conductivity of time of advent (changing into the time: divide) of voltage 400V and 20 ℃ (than conductivity: mS/cm). these measured values are also put down in writing in the lump.
[comparative example 4]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 440V, change into the time: 5.4 minutes, conductivity: 1.4mS/cm
[embodiment 27]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Ethylene glycol (77 weight %)
Dimethyl adipate (10 weight %)
Water (3 weight %)
Sparking voltage: 470V, change into the time: 4.6 minutes, conductivity: 1.4mS/cm
[embodiment 28]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Ethylene glycol (84 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 4.5 minutes, conductivity: 1.4mS/cm
[embodiment 29]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Ethylene glycol (77 weight %)
11-cyano group 11 (carbon) alkanoic acid methyl esters (10 weight %)
Water (3 weight %)
Sparking voltage: 475V, change into the time: 4.7 minutes, conductivity: 1.3mS/cm
[embodiment 30]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Ethylene glycol (82 weight %)
Nonyl lactone (5 weight %)
Water (3 weight %)
Sparking voltage: 465V, change into the time: 4.7 minutes, conductivity: 1.4mS/cm
[embodiment 31]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Ethylene glycol (74 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Own dicyan (10 weight %)
Water (3 weight %)
Sparking voltage: 500V, change into the time: 4.7 minutes, conductivity: 1.3mS/cm
[embodiment 32]
1,6-decane dicarboxylic acid ammonium (5 weight %)
11-cyano group 11 (carbon) alkanoic acid ammonium (5 weight %)
Ethylene glycol (84 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 500V, change into the time: 8.8 minutes, conductivity: 1.4mS/cm
[embodiment 33]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Trimethylace tonitric ammonium (5 weight %)
Ethylene glycol (79 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 485V, change into the time: 4.8 minutes, conductivity: 1.6mS/cm
[embodiment 34]
1,6-decane dicarboxylic acid ammonium (7.5 weight %)
Trimethylace tonitric ammonium (7.5 weight %)
Ethylene glycol (79 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 500V, change into the time: 5.1 minutes, conductivity: 1.7mS/cm
[embodiment 35]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (79 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 505V, change into the time: 5.2 minutes, conductivity: 1.7mS/cm
[embodiment 36]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (54 weight %)
Gamma-butyrolacton (25 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 505V, change into the time: 4.9 minutes, conductivity: 1.7mS/cm
[embodiment 37]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (69 weight %)
11-cyano group 11 (carbon) alkanoic acid methyl esters (10 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 495V, change into the time: 4.9 minutes, conductivity: 1.6mS/cm
[embodiment 38]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Trimethylace tonitric ammonium (10 weight %)
Ethylene glycol (69 weight %)
Own dicyan (10 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 510V, change into the time: 5.0 minutes, conductivity: 1.7mS/cm
[embodiment 39]
1,6-decane dicarboxylic acid ammonium (5 weight %)
2,2-diisopropyl propionic acid ammonium (10 weight %)
Ethylene glycol (39 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Gamma-butyrolacton (25 weight %)
Own dicyan (15 weight %)
Water (3 weight %)
Sparking voltage: 510V, change into the time: 4.9 minutes, conductivity: 1.8mS/cm
The result of comparing embodiment 27～39 and comparative example 4 as a result the time as can be known, according to the present invention, add 1,6-decane dicarboxylic acid ammonium and diester compound, the lactone compound with alkyl or cyano group alkanisation compound are (as required, also nitrile compound can be arranged) as the electrolyte of adding ingredient, and only add 1, the electrolyte of 6-decane dicarboxylic acid ammonium is compared, changing into time and conductivity does not have big change, but sparking voltage has improved significantly.
Below, in the water-containing organic solvent that constitutes by ethylene glycol (or ethylene glycol and gamma-butyrolacton) and water, modulation is except 1, beyond the 6-decane dicarboxylic acid ammonium, also adding dissolving has the alkyl chain of 3～7 of carbon numbers and the monocarboxylic acid of alkyl of two carbon numbers 1～4 or the electrolyte of its salt is arranged in the β position of carboxyl, and aluminium foil is immersed in this electrolyte, and be determined at 10mA/cm
2Current density under when changing into constant current sparking voltage (V), reach the following conductivity of time of advent (changing into the time: divide) of voltage 400V and 20 ℃ (than conductivity: mS/cm). these measured values are also put down in writing in the lump.
[embodiment 40]
1,6-decane dicarboxylic acid ammonium (7.5 weight %)
3,3-acid dimethyl ammonium (2.5 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 5.7 minutes, conductivity: 1.5mS/cm
[embodiment 41]
1,6-decane dicarboxylic acid ammonium (5 weight %)
3,3-acid dimethyl ammonium (5 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 500V, change into the time: 6.0 minutes, conductivity: 1.5mS/cm
[embodiment 42]
1,6-decane dicarboxylic acid ammonium (2.5 weight %)
3,3-acid dimethyl ammonium (7.5 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 510V, change into the time: 6.2 minutes, conductivity: 1.6mS/cm
[embodiment 43]
1,6-decane dicarboxylic acid ammonium (2.5 weight %)
3,3-acid dimethyl ammonium (7.5 weight %)
Ethylene glycol (70 weight %)
Adiponitrile (17 weight %)
Water (3 weight %)
Sparking voltage: 550V, change into the time: 6.1 minutes, conductivity: 1.4mS/cm
[embodiment 44]
1,6-decane dicarboxylic acid ammonium (2.5 weight %)
3,3-acid dimethyl ammonium (7.5 weight %)
Ethylene glycol (22 weight %)
Gamma-butyrolacton (50 weight %)
Adiponitrile (15 weight %)
Water (3 weight %)
Sparking voltage: 560V, change into the time: 5.8 minutes, conductivity: 1.5mS/cm
[embodiment 45]
1,6-decane dicarboxylic acid ammonium (2.5 weight %)
3,3-acid dimethyl ammonium (7.5 weight %)
Ethylene glycol (17 weight %)
Gamma-butyrolacton (50 weight %)
γ-11 (carbon) alkanoic acid lactone (5 weight %)
Adiponitrile (15 weight %)
Water (3 weight %)
Sparking voltage: 560V, change into the time: 5.3 minutes, conductivity: 1.5mS/cm
The result of comparing embodiment 40～45 and comparative example 4 as a result the time as can be known, according to the present invention, add 1,6-decane dicarboxylic acid ammonium and have the alkyl chain of 3～7 of carbon numbers and the monocarboxylic acid of alkyl of two carbon numbers 1～4 is arranged in the β position of carboxyl or its salt (according to circumstances, also nitrile compound can be arranged) as the electrolyte of adding ingredient, and only add 1, the electrolyte of 6-decane dicarboxylic acid ammonium is compared, changing into time and conductivity does not have big change, but sparking voltage has improved significantly.
Below, in the water-containing organic solvent that constitutes by ethylene glycol and water, modulation is except 1, beyond the 6-decane dicarboxylic acid ammonium, also adding monocarboxylic acid or its salt that there is an ethyl α position be dissolved in carboxyl or becoming the ring carbon atom number is 5 or 6 the ring-type saturated compounds monocarboxylic acid or the electrolyte of its salt, and aluminium foil is immersed in this electrolyte, and be determined at 10mA/cm
2Current density under when changing into constant current sparking voltage (V), reach the following conductivity of time of advent (changing into the time: divide) of voltage 400V and 20 ℃ (than conductivity: mS/cm). these measured values are also put down in writing in the lump.
[comparative example 5]
1,6-decane dicarboxylic acid ammonium (10 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 440V, change into the time: 5.7 minutes, conductivity: 1.4mS/cm
[comparative example 6]
2 Ethylbutanoic acid ammonium (10 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 330V, change into the time: 9.2 minutes, conductivity: 1.6mS/cm
[comparative example 7]
2-ethyl acid ammonium (10 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 355V, change into the time: 12.2 minutes, conductivity: 1.0mS/cm
[comparative example 8]
Ring ammonium valerate (10 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 405V, change into the time: 13.2 minutes, conductivity: 1.6mS/cm
[comparative example 9]
Cyclohexylpentanoic acid ammonium (10 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 480V, change into the time: 18.9 minutes, conductivity: 1.5mS/cm
[embodiment 46]
1,6-decane dicarboxylic acid ammonium (5 weight %)
2 Ethylbutanoic acid ammonium (5 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 490V, change into the time: 5.6 minutes, conductivity: 1.4mS/cm
[embodiment 47]
1,6-decane dicarboxylic acid ammonium (5 weight %)
2-ethyl acid ammonium (5 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 520V, change into the time: 6.5 minutes, conductivity: 1.3mS/cm
[embodiment 48]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Ring ammonium valerate (5 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 495V, change into the time: 6.2 minutes, conductivity: 1.5mS/cm
[embodiment 49]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Cyclohexylpentanoic acid ammonium (5 weight %)
Ethylene glycol (87 weight %)
Water (3 weight %)
Sparking voltage: 495V, change into the time: 6.0 minutes, conductivity: 1.4mS/cm
[embodiment 50]
1,6-decane dicarboxylic acid ammonium (5 weight %)
2-ethyl acid ammonium (5 weight %)
Ethylene glycol (77 weight %)
Adiponitrile (10 weight %)
Water (3 weight %)
Sparking voltage: 520V, change into the time: 5.9 minutes, conductivity: 1.5mS/cm
[embodiment 51]
1,6-decane dicarboxylic acid ammonium (5 weight %)
2-ethyl acid ammonium (5 weight %)
Ethylene glycol (74 weight %)
Adiponitrile (10 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 530V, change into the time: 5.9 minutes, conductivity: 1.5mS/cm
[embodiment 52]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Cyclohexylpentanoic acid ammonium (5 weight %)
Ethylene glycol (77 weight %)
Adiponitrile (10 weight %)
Water (3 weight %)
Sparking voltage: 510V, change into the time: 5.9 minutes, conductivity: 1.6mS/cm
[embodiment 53]
1,6-decane dicarboxylic acid ammonium (5 weight %)
Cyclohexylpentanoic acid ammonium (5 weight %)
Ethylene glycol (74 weight %)
Adiponitrile (10 weight %)
γ-11 (carbon) alkanoic acid lactone (3 weight %)
Water (3 weight %)
Sparking voltage: 520V, change into the time: 5.9 minutes, conductivity: 1.6mS/cm
The result of comparing embodiment 46～53 and comparative example 4～9 as a result the time as can be known, according to the present invention, add 1,6-decane dicarboxylic acid ammonium with α position monocarboxylic acid or its salt of an ethyl is arranged at carboxyl or become the ring carbon atom number be 5 or 6 ring-type saturated compounds monocarboxylic acid or its salt (according to circumstances, also nitrile compound can be arranged) as the electrolyte of adding ingredient, with only add 1, the electrolyte of 6-decane dicarboxylic acid ammonium is compared, changing into time and conductivity does not have big change, but sparking voltage has improved significantly.
Industrial applicibility
Electrolyte in the time of this and electrolytic capacitor can be easily used as air conditioner, freezer, high frequency electronics heating of food device, washing machine, illumination apparatus, elevator, robot, NC working machine, electric car, also have the driving power of solar power generation, differential locomotive, electric vapour automobile etc.
Claims (4)
1. decane dicarboxylic acid composition, it is made of following compositions:
1,6-decane dicarboxylic acid or its salt and
1,10-decane dicarboxylic acid and/or its salt,
Wherein, 1, the mixing amount of 10-decane dicarboxylic acid and/or its salt is with respect to 1, and the weight of 6-decane dicarboxylic acid or its salt is below the 3 weight %.
2. the described decane dicarboxylic acid composition of claim 1, wherein, 1, the mixing amount of 10-decane dicarboxylic acid and/or its salt is with respect to 1, and the weight of 6-decane dicarboxylic acid or its salt is below the 1 weight %.
3. the described decane dicarboxylic acid preparation of compositions of claim 1 method, it may further comprise the steps:
To comprise 1,6-decane dicarboxylic acid and 1, the composition esterification of 10-decane dicarboxylic acid is to obtain comprising 1, the ester of 6-decane dicarboxylic acid and 1, the ester composition of the ester of 10-decane dicarboxylic acid;
Distill this ester composition and comprise 1, the distillate of the ester of 6-decane dicarboxylic acid with recovery; With
1 of recovery, the ester of 6-decane dicarboxylic acid are somebody's turn to do in hydrolysis.
4. the described method of claim 3, wherein, described ester composition is the composition of methyl ester, the composition of ethyl ester, the composition of straight or branched propyl diester or the composition of straight or branched butyl ester.
Applications Claiming Priority (18)
| Application Number | Priority Date | Filing Date | Title |
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| JP2001006204 | 2001-01-15 | ||
| JP2001006204 | 2001-01-15 | ||
| JP2001-006204 | 2001-01-15 | ||
| JP2001211729 | 2001-07-12 | ||
| JP2001211729 | 2001-07-12 | ||
| JP2001-211729 | 2001-07-12 | ||
| JP2001213227A JP4517544B2 (en) | 2001-01-15 | 2001-07-13 | Electrolytic solution for electrolytic capacitor and electrolytic capacitor using the same |
| JP2001-213227 | 2001-07-13 | ||
| JP2001213227 | 2001-07-13 | ||
| JP2001219525 | 2001-07-19 | ||
| JP2001219525 | 2001-07-19 | ||
| JP2001-219525 | 2001-07-19 | ||
| JP2001235865 | 2001-08-03 | ||
| JP2001235865 | 2001-08-03 | ||
| JP2001-235865 | 2001-08-03 | ||
| JP2001268524 | 2001-09-05 | ||
| JP2001-268524 | 2001-09-05 | ||
| JP2001268524 | 2001-09-05 |
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| CNB028058836A Division CN100440397C (en) | 2001-01-15 | 2002-01-15 | Electrolysis solution for electrolytic capacitors |
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| CN1230001A (en) * | 1998-03-23 | 1999-09-29 | 松下电器产业株式会社 | Aluminium electrolysis capacitor |
| CN1261720A (en) * | 1998-12-01 | 2000-08-02 | 如碧空株式会社 | Electrolyte solution and electrolyte capacitor using said electrolyte solution |
| CN1275239A (en) * | 1998-12-01 | 2000-11-29 | 如碧空株式会社 | Electrolyte for driving electrolytic capacitor and electrolytic capacitor |
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| JPS6085509A (en) * | 1983-10-17 | 1985-05-15 | 岡村製油株式会社 | Electrolyte for driving electrolytic condenser |
| JP3780703B2 (en) * | 1997-06-20 | 2006-05-31 | 宇部興産株式会社 | Method for producing 2-butyloctanedioic acid |
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|---|---|---|---|---|
| CN1230001A (en) * | 1998-03-23 | 1999-09-29 | 松下电器产业株式会社 | Aluminium electrolysis capacitor |
| CN1261720A (en) * | 1998-12-01 | 2000-08-02 | 如碧空株式会社 | Electrolyte solution and electrolyte capacitor using said electrolyte solution |
| CN1275239A (en) * | 1998-12-01 | 2000-11-29 | 如碧空株式会社 | Electrolyte for driving electrolytic capacitor and electrolytic capacitor |
Non-Patent Citations (2)
| Title |
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| JP特开2000-348982A 2000.12.15 |
| JP特开平8-8147A 1996.01.12 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101383227A (en) | 2009-03-11 |
| JP2010004084A (en) | 2010-01-07 |
| JP4947117B2 (en) | 2012-06-06 |
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