CN107331514B - - 40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind and preparation method thereof - Google Patents
- 40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind and preparation method thereof Download PDFInfo
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- CN107331514B CN107331514B CN201710525590.3A CN201710525590A CN107331514B CN 107331514 B CN107331514 B CN 107331514B CN 201710525590 A CN201710525590 A CN 201710525590A CN 107331514 B CN107331514 B CN 107331514B
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- 238000005868 electrolysis reaction Methods 0.000 title claims abstract description 37
- 239000007788 liquid Substances 0.000 title claims abstract description 37
- 238000002360 preparation method Methods 0.000 title abstract description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 120
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 48
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 32
- 238000004078 waterproofing Methods 0.000 claims abstract description 31
- FLDCSPABIQBYKP-UHFFFAOYSA-N 5-chloro-1,2-dimethylbenzimidazole Chemical compound ClC1=CC=C2N(C)C(C)=NC2=C1 FLDCSPABIQBYKP-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000001741 Ammonium adipate Substances 0.000 claims abstract description 27
- 235000019293 ammonium adipate Nutrition 0.000 claims abstract description 27
- VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000002994 raw material Substances 0.000 claims abstract description 23
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 22
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims abstract description 20
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000000908 ammonium hydroxide Substances 0.000 claims abstract description 20
- 239000008367 deionised water Substances 0.000 claims abstract description 20
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 20
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims abstract description 20
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims description 66
- 239000000654 additive Substances 0.000 claims description 56
- 230000000996 additive effect Effects 0.000 claims description 56
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 239000001257 hydrogen Substances 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 15
- 239000003381 stabilizer Substances 0.000 claims description 15
- 229920001451 polypropylene glycol Polymers 0.000 claims description 13
- 150000007942 carboxylates Chemical class 0.000 claims description 10
- 230000032050 esterification Effects 0.000 claims description 10
- 238000005886 esterification reaction Methods 0.000 claims description 10
- 102000004160 Phosphoric Monoester Hydrolases Human genes 0.000 claims description 9
- 108090000608 Phosphoric Monoester Hydrolases Proteins 0.000 claims description 9
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 9
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 claims description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 7
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 7
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 7
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 7
- 238000007664 blowing Methods 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 7
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 7
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 7
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 7
- 238000004321 preservation Methods 0.000 claims description 7
- 229950000244 sulfanilic acid Drugs 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- 238000005303 weighing Methods 0.000 claims 6
- 239000003990 capacitor Substances 0.000 abstract description 21
- 239000003792 electrolyte Substances 0.000 abstract description 16
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 11
- 229910052782 aluminium Inorganic materials 0.000 abstract description 11
- 238000004519 manufacturing process Methods 0.000 abstract description 10
- -1 2- butyl -2- ethyl Chemical group 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 7
- CFBYEGUGFPZCNF-UHFFFAOYSA-N 2-nitroanisole Chemical compound COC1=CC=CC=C1[N+]([O-])=O CFBYEGUGFPZCNF-UHFFFAOYSA-N 0.000 description 6
- OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 description 6
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 6
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 6
- BVPWNLKBGNMZRI-UHFFFAOYSA-N decanedioic acid;2,2-dimethylpropane-1,3-diol Chemical compound OCC(C)(C)CO.OC(=O)CCCCCCCCC(O)=O BVPWNLKBGNMZRI-UHFFFAOYSA-N 0.000 description 6
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 6
- 229960001484 edetic acid Drugs 0.000 description 6
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical class OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 6
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- QRDZFPUVLYEQTA-UHFFFAOYSA-N quinoline-8-carboxylic acid Chemical compound C1=CN=C2C(C(=O)O)=CC=CC2=C1 QRDZFPUVLYEQTA-UHFFFAOYSA-N 0.000 description 6
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 239000004411 aluminium Substances 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 238000013329 compounding Methods 0.000 description 5
- 230000005611 electricity Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 230000000887 hydrating effect Effects 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- OARDBPIZDHVTCK-UHFFFAOYSA-N 2-butyloctanoic acid Chemical compound CCCCCCC(C(O)=O)CCCC OARDBPIZDHVTCK-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 206010054949 Metaplasia Diseases 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- OTRAYOBSWCVTIN-UHFFFAOYSA-N OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O.N.N.N.N.N.N.N.N.N.N.N.N.N.N.N Chemical compound OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O.N.N.N.N.N.N.N.N.N.N.N.N.N.N.N OTRAYOBSWCVTIN-UHFFFAOYSA-N 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000001535 kindling effect Effects 0.000 description 1
- 230000015689 metaplastic ossification Effects 0.000 description 1
- 230000000452 restraining effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/022—Electrolytes; Absorbents
- H01G9/035—Liquid electrolytes, e.g. impregnating materials
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/145—Liquid electrolytic capacitors
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The present invention relates to technical field of electrolyte, more particularly to a kind of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid and preparation method thereof, which includes the raw material of following parts by weight: 8-12 parts of glycol monoethyl ether, 7-11 parts of ammonium adipate, 6-10 parts of ethylene glycol, 6-10 parts of waterproofing agent, 1-3 parts of ammonium formate, phosphoric acid 0.5-1.5,0.5-1.5 parts of p-nitrophenyl first ammonium, 0.5-1.5 parts of ammonium hydroxide, 40-80 parts of deionized water.Electrolyte flash over voltage of the invention can achieve 105V, conductivity can achieve 40ms/cm, and -40 DEG C of condenser capacity decaying are less than 20%, have good electrochemical properties, have the advantages that high conductivity, Low ESR and low pressure, can be applied to the manufacture of low-voltage aluminum electrolytic capacitor.
Description
Technical field
The present invention relates to technical field of electrolyte, and in particular to -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind and its system
Preparation Method.
Background technique
Aluminium electrolutic capacitor is one of base components of electronic product.With the continuous improvement of Quality of electronic products and aluminium electricity
The expansion of electrolysis condenser application range puts forward higher requirements its performance.The electronic products such as Switching Power Supply, energy-saving lamp are to high pressure
The security performance of electrolytic capacitor requires very high.In filter circuit, capacitor bears high voltage, high ripple current, if feed
Unstable or application overvoltage, that is, can lead to the accidents such as the destruction, kindling, burning of capacitor.Aluminum electrolytic capacitor electrolyte is electricity
Practical cathode in container whole work process, has a major impact the performance of capacitor, in which: use temperature range, work
Service life, reliability, leakage current, loss, volume change etc. play a decisive role to electrical property.
At present it is known that or medium-high voltage aluminum electrolytic capacitor Working electrolyte, have passed through following development
Process: one, using ethylene glycol as main solvent, the inorganic compounds such as boric acid or ammonium pentaborate are main solute.The work electricity prepared in this way
Solution liquid has that conductivity is low, and boric acid and its salt easily occur esterification with ethylene glycol at high temperature and generates a large amount of
Condensation water, cause the moisture content inside electrolyte to increase, the vapour pressure of electrolyte increases, and capacitor internal pressure increases and causes
The failure of capacitor valve opening;Two, using ethylene glycol as main solvent, using the direct-connected hydrocarbon saturation two such as azelaic acid, decanedioic acid or 12 diacid
Carboxylic acid and its salt are electrolyte solution, although this kind of electrolyte avoids a part of esterification, but due to this
Solubility of a kind of linear paraffin in ethylene glycol is smaller, causes the impedance of product larger, is easy fever under big ripple and makes
Solvent volatilization causes capacitor withered and fails, while amide easily occurs at high temperature for linear paraffin to generate vicious circle
Change side reaction and generate water, also easily causes capacitor initial failure;Three, using some branched acid or its salt, 1 such as reported,
6-DDA and its salt and 2- butyl octanoic acid and its salt, this kind of branched carboxylic acid and its salt compare straight chain to the solubility of solvent
Alkane increases, thus produces effect to a certain extent, but simultaneously, and this kind of acid or its salt rely primarily on import, because forming
This height and restraining factors are more.
Summary of the invention
In order to overcome shortcoming and defect existing in the prior art, the purpose of the present invention is to provide a kind of -40 DEG C of overclockings
Low ESR low-voltage electrolysis liquid, the electrolyte flash over voltage can achieve 105V, and conductivity can achieve 40ms/cm, -40 DEG C of capacitors
Device capacity attenuation is less than 20%, has good electrochemical properties, has the advantages that high conductivity, Low ESR and low pressure, can apply
In the manufacture of low-voltage aluminum electrolytic capacitor.
Another object of the present invention is to provide a kind of preparation method of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid, the systems
Preparation Method simple process, convenient operation and control, quality are stablized, and high production efficiency, production cost is low, can large-scale industry metaplasia
It produces.
The purpose of the invention is achieved by the following technical solution: a kind of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid, including such as
The raw material of lower parts by weight:
8-12 parts of glycol monoethyl ether
7-11 parts of ammonium adipate
6-10 parts of ethylene glycol
6-10 parts of waterproofing agent
1-3 parts of ammonium formate
0.5-1.5 parts of phosphoric acid
0.5-1.5 parts of p-nitrophenyl first ammonium
0.5-1.5 parts of ammonium hydroxide
40-80 parts of deionized water.
Electrolyte of the invention is by using the interaction between above-mentioned raw materials, and the weight of each raw material of strict control is matched
Than electrolyte flash over voltage obtained can achieve 105V, and conductivity can achieve 40ms/cm, -40 DEG C of condenser capacity decaying
Less than 20%, there are good electrochemical properties, have the advantages that high conductivity, Low ESR and low pressure, can be applied to low pressure aluminium electricity
The manufacture of electrolysis condenser.
Preferably, the raw material including following parts by weight:
8-10 parts of glycol monoethyl ether
7-9 parts of ammonium adipate
6-8 parts of ethylene glycol
6-8 parts of waterproofing agent
1-2 parts of ammonium formate
0.5-1.0 parts of phosphoric acid
0.5-1.0 parts of p-nitrophenyl first ammonium
0.5-1.0 parts of ammonium hydroxide
40-60 parts of deionized water.
Preferably, the raw material including following parts by weight:
9-11 parts of glycol monoethyl ether
8-10 parts of ammonium adipate
7-9 parts of ethylene glycol
7-9 parts of waterproofing agent
1.5-2.5 parts of ammonium formate
0.8-1.2 parts of phosphoric acid
0.8-1.2 parts of p-nitrophenyl first ammonium
0.8-1.2 parts of ammonium hydroxide
50-70 parts of deionized water.
Preferably, the raw material including following parts by weight:
10-12 parts of glycol monoethyl ether
9-11 parts of ammonium adipate
8-10 parts of ethylene glycol
8-10 parts of waterproofing agent
2-3 parts of ammonium formate
.0-1.5 parts of phosphatase 11
1.0-1.5 parts of p-nitrophenyl first ammonium
1.0-1.5 parts of ammonium hydroxide
60-80 parts of deionized water.
Preferably, the raw material including following parts by weight:
9 parts of glycol monoethyl ether
8 parts of ammonium adipate
7 parts of ethylene glycol
7 parts of waterproofing agent
1.5 parts of ammonium formate
0.8 part of phosphoric acid
0.8 part of p-nitrophenyl first ammonium
0.8 part of ammonium hydroxide
50 parts of deionized water.
Preferably, the raw material including following parts by weight:
10 parts of glycol monoethyl ether
9 parts of ammonium adipate
8 parts of ethylene glycol
8 parts of waterproofing agent
2 parts of ammonium formate
.0 parts of phosphatase 11
1.0 parts of p-nitrophenyl first ammonium
1.0 parts of ammonium hydroxide
60 parts of deionized water.
Preferably, the raw material including following parts by weight:
11 parts of glycol monoethyl ether
10 parts of ammonium adipate
9 parts of ethylene glycol
9 parts of waterproofing agent
2.5 parts of ammonium formate
.2 parts of phosphatase 11
1.2 parts of p-nitrophenyl first ammonium
1.2 parts of ammonium hydroxide
70 parts of deionized water.
Preferably, the waterproofing agent be by ethylene glycol, hydroxycarboxylic acid and phosphide by weight 5-7:1.5-2.5:1 in
Esterification 3-4h is made at a temperature of 120-170 DEG C.
Preferably, the waterproofing agent is by weight 6:2:1 by ethylene glycol, hydroxycarboxylic acid and phosphide in 145 DEG C of temperature
Lower esterification 3.5h is made.
Further include 3-5 parts of high polymer additive, hinder 2-4 parts of carboxylate agent, 1-3 parts of high-temperature stabilizer, anti-corrosion addition
1-2 parts of agent, 1-2 parts of scintillation additive and disappear 0.5-1.5 parts of hydrogen additive.
The high polymer additive is by polyvinyl alcohol, polypropylene glycol and ethylene oxide and propylene oxide copolymers with weight
Than the mixture of 0.4-0.8:0.8-1.2:1 composition.The present invention passes through the type of strict control high polymer additive, compounds and match
Than that can shield extra electric field, protect the dielectric properties of deielectric-coating, because of both or two or more organic big point to dissolve each other
The viscosity of electrolyte solution is adjusted in sub- collective effect, reduces the saturated vapour pressure of capacitor internal, improves flash over voltage, improves
Stability.
The obstruction carboxylate agent is by 2- butyl -2- ethyl -1,3-PD, 2- butyl -2- methyl-1,3- third
The mixture that two pure and mild neopentyl glycols are formed with weight ratio 1:0.4-0.8:0.2-0.6.The present invention hinders carboxylic by strict control
Type, compounding and the proportion of acid esters agent, can hinder carboxylic esterification.
The high-temperature stabilizer is by polyvinyl acetal, polyvinylpyrrolidone and p-aminobenzene sulfonic acid with weight ratio
The mixture of 0.5-1.5:1:1.5-2.5 composition.The present invention passes through type, compounding and the proportion of strict control high-temperature stabilizer,
The high temperature resistant service life of electrolyte can be improved.
The anticorrosive additive is by ethylenediamine tetra-acetic acid, 8- carboxyl quinoline and metasilicic acid ammonium with weight ratio 1:0.8-1.2:
1.5-2.5 the mixture of composition.The present invention passes through type, compounding and the proportion of strict control anticorrosive additive, it is possible to reduce electricity
Solve corrosion of the liquid to capacitor.
The scintillation additive is selected from poly- 1,4- succinate, poly- neopentyl glycol sebacate, POLYPROPYLENE GLYCOL and polyethylene
The mixture that butyral is formed with weight ratio 1:1.4-1.8:1.5-2.5.The present invention passes through strict control scintillation additive kind
The flash over voltage of electrolyte can be improved to enhance the effect of aluminium electrolutic capacitor voltage endurance capability in class, compounding and proportion.
The hydrogen additive that disappears is by ortho-nitroanisole, paranitrobenzoic acid ammonium and 2,4,6- trinitrophenol with weight
Than the mixture of 0.4-0.8:0.8-1.2:1 composition.The present invention is disappeared hydrogen additive types, compounding and proportion by strict control,
Electrolyte can be improved disappears Hydrogen Energy power to reduce aluminium electrolutic capacitor production gas and play drum failure phenomenon.
Another object of the present invention is achieved through the following technical solutions: -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind
Preparation method, by ammonium formate, ammonium adipate, ethylene glycol and waterproofing agent Hybrid Heating to 120-130 DEG C of heat preservation 25-35min, then plus
Enter surplus stock, 55-65 DEG C of constant temperature 12-18min, -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid are made in blowing.
The beneficial effects of the present invention are: electrolyte flash over voltage of the invention can achieve 105V, and conductivity can reach
To 40ms/cm, -40 DEG C of condenser capacity decaying are less than 20%, have good electrochemical properties, have high conductivity, Low ESR
And the advantages of low pressure, it can be applied to the manufacture of low-voltage aluminum electrolytic capacitor.
Preparation method simple process of the invention, convenient operation and control, quality are stablized, and high production efficiency, production cost is low,
It can large-scale industrial production.
Specific embodiment
For the ease of the understanding of those skilled in the art, below with reference to embodiment, the present invention is further illustrated, real
The content that the mode of applying refers to not is limitation of the invention.
Embodiment 1
A kind of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid, the raw material including following parts by weight:
8 parts of glycol monoethyl ether
7 parts of ammonium adipate
6 parts of ethylene glycol
6 parts of waterproofing agent
1 part of ammonium formate
0.5 part of phosphoric acid
0.5 part of p-nitrophenyl first ammonium
0.5 part of ammonium hydroxide
40 parts of deionized water.
The waterproofing agent be by ethylene glycol, hydroxycarboxylic acid and phosphide by weight 5-7:1.5:1 the rouge at a temperature of 120 DEG C
Change 3h to be made.
A kind of preparation method of -40 DEG C of overclockings Low ESR low-voltage electrolysis liquid by ammonium formate, ammonium adipate, ethylene glycol and is prevented
Aqua Hybrid Heating adds surplus stock, 55 DEG C of constant temperature 12min to 120 DEG C of heat preservation 25min, and -40 DEG C of overclockings are made in blowing
Low ESR low-voltage electrolysis liquid.
Embodiment 2
A kind of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid, the raw material including following parts by weight:
9 parts of glycol monoethyl ether
8 parts of ammonium adipate
7 parts of ethylene glycol
7 parts of waterproofing agent
1.5 parts of ammonium formate
0.8 part of phosphoric acid
0.8- parts of p-nitrophenyl first ammonium
0.8 part of ammonium hydroxide
50 parts of deionized water.
The waterproofing agent be by ethylene glycol, hydroxycarboxylic acid and phosphide by weight 5-7:1.8:1 the rouge at a temperature of 130 DEG C
Change 3.5h to be made.
A kind of preparation method of -40 DEG C of overclockings Low ESR low-voltage electrolysis liquid by ammonium formate, ammonium adipate, ethylene glycol and is prevented
Aqua Hybrid Heating adds surplus stock, 58 DEG C of constant temperature 14min to 122 DEG C of heat preservation 28min, and -40 DEG C of overclockings are made in blowing
Low ESR low-voltage electrolysis liquid.
Embodiment 3
A kind of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid, the raw material including following parts by weight:
10 parts of glycol monoethyl ether
9 parts of ammonium adipate
8 parts of ethylene glycol
8 parts of waterproofing agent
2 parts of ammonium formate
.0 parts of phosphatase 11
1.0 parts of p-nitrophenyl first ammonium
1.0 parts of ammonium hydroxide
60 parts of deionized water.
The waterproofing agent is esterified at a temperature of 145 DEG C by weight 6:2:1 by ethylene glycol, hydroxycarboxylic acid and phosphide
3.5h being made.
A kind of preparation method of -40 DEG C of overclockings Low ESR low-voltage electrolysis liquid by ammonium formate, ammonium adipate, ethylene glycol and is prevented
Aqua Hybrid Heating adds surplus stock, 60 DEG C of constant temperature 15min to 125 DEG C of heat preservation 30min, and -40 DEG C of overclockings are made in blowing
Low ESR low-voltage electrolysis liquid.
Embodiment 4
A kind of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid, the raw material including following parts by weight:
11 parts of glycol monoethyl ether
10 parts of ammonium adipate
9 parts of ethylene glycol
9 parts of waterproofing agent
2.5 parts of ammonium formate
.2 parts of phosphatase 11
1.2 parts of p-nitrophenyl first ammonium
1.2 parts of ammonium hydroxide
70 parts of deionized water.
The waterproofing agent be by ethylene glycol, hydroxycarboxylic acid and phosphide by weight 5-7:2.2:1 the rouge at a temperature of 160 DEG C
Change 3.5h to be made.
A kind of preparation method of -40 DEG C of overclockings Low ESR low-voltage electrolysis liquid by ammonium formate, ammonium adipate, ethylene glycol and is prevented
Aqua Hybrid Heating adds surplus stock, 62 DEG C of constant temperature 16min to 128 DEG C of heat preservation 32min, and -40 DEG C of overclockings are made in blowing
Low ESR low-voltage electrolysis liquid.
Embodiment 5
A kind of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid, the raw material including following parts by weight:
12 parts of glycol monoethyl ether
11 parts of ammonium adipate
10 parts of ethylene glycol
10 parts of waterproofing agent
3 parts of ammonium formate
.5 parts of phosphatase 11
1.5 parts of p-nitrophenyl first ammonium
1.5 parts of ammonium hydroxide
80 parts of deionized water.
The waterproofing agent be by ethylene glycol, hydroxycarboxylic acid and phosphide by weight 5-7:2.5:1 at a temperature of 170 DEG C
Esterified 4h is made.
A kind of preparation method of -40 DEG C of overclockings Low ESR low-voltage electrolysis liquid by ammonium formate, ammonium adipate, ethylene glycol and is prevented
Aqua Hybrid Heating adds surplus stock, 65 DEG C of constant temperature 18min to 130 DEG C of heat preservation 35min, and -40 DEG C of overclockings are made in blowing
Low ESR low-voltage electrolysis liquid.
Embodiment 6
The present embodiment and above-described embodiment the difference is that: further include 3 parts of high polymer additive, hinder carboxylic esterification
2 parts of agent, 1 part of high-temperature stabilizer, 1 part of anticorrosive additive, 1 part of scintillation additive, disappear 0.5 part of hydrogen additive and 1 part of waterproof mixture.
The high polymer additive is by polyvinyl alcohol, polypropylene glycol and ethylene oxide and propylene oxide copolymers with weight
Than the mixture of 0.4:0.8:1 composition.
The obstruction carboxylate agent is the 3- the third two by 2- butyl -2- ethyl -1,3-PD, 2- butyl -2- methyl-1
The mixture that pure and mild neopentyl glycol is formed with weight ratio 1:0.4:0.2.
The high-temperature stabilizer is by polyvinyl acetal, polyvinylpyrrolidone and p-aminobenzene sulfonic acid with weight ratio
The mixture of 0.5-1.5:1:1.5-2.5 composition.
The anticorrosive additive is by ethylenediamine tetra-acetic acid, 8- carboxyl quinoline and metasilicic acid ammonium with weight ratio 1:0.8:1.5
The mixture of composition.
The scintillation additive is selected from poly- 1,4- succinate, poly- neopentyl glycol sebacate, POLYPROPYLENE GLYCOL and polyethylene
The mixture that butyral is formed with weight ratio 1:1.4:1.5.
The hydrogen additive that disappears is by ortho-nitroanisole, paranitrobenzoic acid ammonium and 2,4,6- trinitrophenol with weight
Than the mixture of 0.4:0.8:1 composition.
Embodiment 7
The present embodiment and above-described embodiment the difference is that: further include 3.5 parts of high polymer additive, hinder carboxylate
2.5 parts of agent, 1.5 parts of high-temperature stabilizer, 1.2 parts of anticorrosive additive, 1.2 parts of scintillation additive, disappear 0.8 part of hydrogen additive and anti-
1.2 parts of hydrating agents.
The high polymer additive is by polyvinyl alcohol, polypropylene glycol and ethylene oxide and propylene oxide copolymers with weight
Than the mixture of 0.5:0.9:1 composition.
The obstruction carboxylate agent is the 3- the third two by 2- butyl -2- ethyl -1,3-PD, 2- butyl -2- methyl-1
The mixture that pure and mild neopentyl glycol is formed with weight ratio 1:0.5:0.3.
The high-temperature stabilizer is by polyvinyl acetal, polyvinylpyrrolidone and p-aminobenzene sulfonic acid with weight ratio
The mixture of 0.5-1.5:1:1.5-2.5 composition.
The anticorrosive additive is by ethylenediamine tetra-acetic acid, 8- carboxyl quinoline and metasilicic acid ammonium with weight ratio 1:0.9:1.8
The mixture of composition.
The scintillation additive is selected from poly- 1,4- succinate, poly- neopentyl glycol sebacate, POLYPROPYLENE GLYCOL and polyethylene
The mixture that butyral is formed with weight ratio 1:1.5:1.8.
The hydrogen additive that disappears is by ortho-nitroanisole, paranitrobenzoic acid ammonium and 2,4,6- trinitrophenol with weight
Than the mixture of 0.5:0.9:1 composition.
Embodiment 8
The present embodiment and above-described embodiment the difference is that: further include 4 parts of high polymer additive, hinder carboxylic esterification
3 parts of agent, 2 parts of high-temperature stabilizer, 1.5 parts of anticorrosive additive, 1.5 parts of scintillation additive, disappear 1 part of hydrogen additive and waterproof mixture
1.5 part.
The high polymer additive is by polyvinyl alcohol, polypropylene glycol and ethylene oxide and propylene oxide copolymers with weight
Than the mixture of 0.6:1:1 composition.
The obstruction carboxylate agent is the 3- the third two by 2- butyl -2- ethyl -1,3-PD, 2- butyl -2- methyl-1
The mixture that pure and mild neopentyl glycol is formed with weight ratio 1:0.6:0.4.
The high-temperature stabilizer is by polyvinyl acetal, polyvinylpyrrolidone and p-aminobenzene sulfonic acid with weight ratio
The mixture of 1:1:2 composition.
The anticorrosive additive is made of ethylenediamine tetra-acetic acid, 8- carboxyl quinoline and metasilicic acid ammonium with weight ratio 1:1:2
Mixture.
The scintillation additive is selected from poly- 1,4- succinate, poly- neopentyl glycol sebacate, POLYPROPYLENE GLYCOL and polyethylene
The mixture that butyral is formed with weight ratio 1:1.6:2.
The hydrogen additive that disappears is by ortho-nitroanisole, paranitrobenzoic acid ammonium and 2,4,6- trinitrophenol with weight
Than the mixture of 0.6:1:1 composition.
Embodiment 9
The present embodiment and above-described embodiment the difference is that: further include 4.5 parts of high polymer additive, hinder carboxylate
3.5 parts of agent, 2.5 parts of high-temperature stabilizer, 1.8 parts of anticorrosive additive, 1.8 parts of scintillation additive, disappear 1.2 parts of hydrogen additive and anti-
1.8 parts of hydrating agents.
The high polymer additive is by polyvinyl alcohol, polypropylene glycol and ethylene oxide and propylene oxide copolymers with weight
Than the mixture of 0.7:1.1:1 composition.
The obstruction carboxylate agent is the 3- the third two by 2- butyl -2- ethyl -1,3-PD, 2- butyl -2- methyl-1
The mixture that pure and mild neopentyl glycol is formed with weight ratio 1:0.7:0.5.
The high-temperature stabilizer is by polyvinyl acetal, polyvinylpyrrolidone and p-aminobenzene sulfonic acid with weight ratio
1.2:1:2.2 the mixture of composition.
The anticorrosive additive is by ethylenediamine tetra-acetic acid, 8- carboxyl quinoline and metasilicic acid ammonium with weight ratio 1:1.1:2.2
The mixture of composition.
The scintillation additive is selected from poly- 1,4- succinate, poly- neopentyl glycol sebacate, POLYPROPYLENE GLYCOL and polyethylene
The mixture that butyral is formed with weight ratio 1:1.7:2.2.
The hydrogen additive that disappears is by ortho-nitroanisole, paranitrobenzoic acid ammonium and 2,4,6- trinitrophenol with weight
Than the mixture of 0.7:1.1:1 composition.
Embodiment 10
The present embodiment and above-described embodiment the difference is that: further include 5 parts of high polymer additive, hinder carboxylic esterification
4 parts of agent, 3 parts of high-temperature stabilizer, 2 parts of anticorrosive additive, 2 parts of scintillation additive, disappear 1.5 parts of hydrogen additive and 2 parts of waterproof mixture.
The high polymer additive is by polyvinyl alcohol, polypropylene glycol and ethylene oxide and propylene oxide copolymers with weight
Than the mixture of 0.8:1.2:1 composition.
The obstruction carboxylate agent is the 3- the third two by 2- butyl -2- ethyl -1,3-PD, 2- butyl -2- methyl-1
The mixture that pure and mild neopentyl glycol is formed with weight ratio 1:0.8:0.6.
The high-temperature stabilizer is by polyvinyl acetal, polyvinylpyrrolidone and p-aminobenzene sulfonic acid with weight ratio
1.5:1:2.5 the mixture of composition.
The anticorrosive additive is by ethylenediamine tetra-acetic acid, 8- carboxyl quinoline and metasilicic acid ammonium with weight ratio 1:1.2:2.5
The mixture of composition.
The scintillation additive is selected from poly- 1,4- succinate, poly- neopentyl glycol sebacate, POLYPROPYLENE GLYCOL and polyethylene
The mixture that butyral is formed with weight ratio 1:1.8:2.5.
The hydrogen additive that disappears is by ortho-nitroanisole, paranitrobenzoic acid ammonium and 2,4,6- trinitrophenol with weight
Than the mixture of 0.8:1.2:1 composition.
Electrolyte flash over voltage of the invention can achieve 105V, and conductivity can achieve 40ms/cm, -40 DEG C of capacitors
Capacity attenuation is less than 20%, has good electrochemical properties, has the advantages that high conductivity, Low ESR and low pressure, can be applied to
The manufacture of low-voltage aluminum electrolytic capacitor.
Above-described embodiment is the preferable implementation of the present invention, and in addition to this, the present invention can be realized with other way,
Do not depart under the premise of present inventive concept it is any obviously replace it is within the scope of the present invention.
Claims (9)
1. a kind of -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid, it is characterised in that: the raw material including following parts by weight:
8-12 parts of glycol monoethyl ether
7-11 parts of ammonium adipate
6-10 parts of ethylene glycol
6-10 parts of waterproofing agent
1-3 parts of ammonium formate
0.5-1.5 parts of phosphoric acid
0.5-1.5 parts of p-nitrophenyl first ammonium
0.5-1.5 parts of ammonium hydroxide
40-80 parts of deionized water;
Further include 3-5 parts of high polymer additive, hinder 2-4 parts of carboxylate agent, 1-3 parts of high-temperature stabilizer, anticorrosive additive 1-2
Part, 1-2 parts of scintillation additive and disappear 0.5-1.5 parts of hydrogen additive;
The high polymer additive is by polyvinyl alcohol, polypropylene glycol and ethylene oxide and propylene oxide copolymers with weight ratio
The mixture of 0.4-0.8:0.8-1.2:1 composition;
The high-temperature stabilizer is by polyvinyl acetal, polyvinylpyrrolidone and p-aminobenzene sulfonic acid with weight ratio 0.5-
1.5:1:1.5-2.5 the mixture of composition;
- 40 DEG C of overclockings Low ESR low-voltage electrolysis liquid is made by following steps:
By ammonium formate, ammonium adipate, ethylene glycol and waterproofing agent Hybrid Heating to 120-130 DEG C of heat preservation 25-35min, add surplus
- 40 DEG C of overclocking Low ESR low-voltage electrolysis liquid are made in remaining raw material, 55-65 DEG C of constant temperature 12-18min, blowing.
2. -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind according to claim 1, it is characterised in that: including weighing as follows
Measure the raw material of part:
8-10 parts of glycol monoethyl ether
7-9 parts of ammonium adipate
6-8 parts of ethylene glycol
6-8 parts of waterproofing agent
1-2 parts of ammonium formate
0.5-1.0 parts of phosphoric acid
0.5-1.0 parts of p-nitrophenyl first ammonium
0.5-1.0 parts of ammonium hydroxide
40-60 parts of deionized water.
3. -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind according to claim 1, it is characterised in that: including weighing as follows
Measure the raw material of part:
9-11 parts of glycol monoethyl ether
8-10 parts of ammonium adipate
7-9 parts of ethylene glycol
7-9 parts of waterproofing agent
1.5-2.5 parts of ammonium formate
0.8-1.2 parts of phosphoric acid
0.8-1.2 parts of p-nitrophenyl first ammonium
0.8-1.2 parts of ammonium hydroxide
50-70 parts of deionized water.
4. -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind according to claim 1, it is characterised in that: including weighing as follows
Measure the raw material of part:
10-12 parts of glycol monoethyl ether
9-11 parts of ammonium adipate
8-10 parts of ethylene glycol
8-10 parts of waterproofing agent
2-3 parts of ammonium formate
.0-1.5 parts of phosphatase 11
1.0-1.5 parts of p-nitrophenyl first ammonium
1.0-1.5 parts of ammonium hydroxide
60-80 parts of deionized water.
5. -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind according to claim 1, it is characterised in that: including weighing as follows
Measure the raw material of part:
9 parts of glycol monoethyl ether
8 parts of ammonium adipate
7 parts of ethylene glycol
7 parts of waterproofing agent
1.5 parts of ammonium formate
0.8 part of phosphoric acid
0.8 part of p-nitrophenyl first ammonium
0.8 part of ammonium hydroxide
50 parts of deionized water.
6. -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind according to claim 1, it is characterised in that: including weighing as follows
Measure the raw material of part:
10 parts of glycol monoethyl ether
9 parts of ammonium adipate
8 parts of ethylene glycol
8 parts of waterproofing agent
2 parts of ammonium formate
.0 parts of phosphatase 11
1.0 parts of p-nitrophenyl first ammonium
1.0 parts of ammonium hydroxide
60 parts of deionized water.
7. -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind according to claim 1, it is characterised in that: including weighing as follows
Measure the raw material of part:
11 parts of glycol monoethyl ether
10 parts of ammonium adipate
9 parts of ethylene glycol
9 parts of waterproofing agent
2.5 parts of ammonium formate
.2 parts of phosphatase 11
1.2 parts of p-nitrophenyl first ammonium
1.2 parts of ammonium hydroxide
70 parts of deionized water.
8. -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind according to claim 1, it is characterised in that: the waterproofing agent
Be by ethylene glycol, hydroxycarboxylic acid and phosphide by weight 5-7:1.5-2.5:1 the esterification 3-4h system at a temperature of 120-170 DEG C
?.
9. -40 DEG C of overclocking Low ESR low-voltage electrolysis liquid of one kind according to claim 1, it is characterised in that: the waterproofing agent
It is that by weight 6:2:1, the esterification 3.5h at a temperature of 145 DEG C is made by ethylene glycol, hydroxycarboxylic acid and phosphide.
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CN101477899B (en) * | 2008-12-29 | 2010-12-29 | 南通江海电容器股份有限公司 | Aluminum electrolysis capacitor working electrolyte for energy saving lamp and preparation thereof |
CN105513799B (en) * | 2015-12-22 | 2018-08-21 | 东莞市久制电子有限公司 | A kind of high water system Al Electrolytic Capacitors with Low Impedance at High Frequency electrolyte and preparation method thereof |
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