CN101987824B - 超级电容器用高纯度导电盐的制备方法 - Google Patents
超级电容器用高纯度导电盐的制备方法 Download PDFInfo
- Publication number
- CN101987824B CN101987824B CN2009100415530A CN200910041553A CN101987824B CN 101987824 B CN101987824 B CN 101987824B CN 2009100415530 A CN2009100415530 A CN 2009100415530A CN 200910041553 A CN200910041553 A CN 200910041553A CN 101987824 B CN101987824 B CN 101987824B
- Authority
- CN
- China
- Prior art keywords
- boron trifluoride
- preparation
- organic solvent
- solution
- hours
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 27
- 239000003990 capacitor Substances 0.000 title abstract description 7
- 150000003839 salts Chemical class 0.000 title description 15
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 claims abstract description 40
- -1 tetrafluoroborate Chemical compound 0.000 claims abstract description 34
- 229910015900 BF3 Inorganic materials 0.000 claims abstract description 20
- 150000001875 compounds Chemical class 0.000 claims abstract description 19
- 239000003960 organic solvent Substances 0.000 claims abstract description 18
- 239000012265 solid product Substances 0.000 claims abstract description 16
- 150000002148 esters Chemical class 0.000 claims abstract description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 75
- 238000006243 chemical reaction Methods 0.000 claims description 51
- 239000007787 solid Substances 0.000 claims description 41
- 239000002253 acid Substances 0.000 claims description 40
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 26
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 22
- 239000000706 filtrate Substances 0.000 claims description 21
- 238000001035 drying Methods 0.000 claims description 19
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 16
- LDDQLRUQCUTJBB-UHFFFAOYSA-N ammonium fluoride Chemical compound [NH4+].[F-] LDDQLRUQCUTJBB-UHFFFAOYSA-N 0.000 claims description 14
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- 239000002879 Lewis base Substances 0.000 claims description 11
- 150000007527 lewis bases Chemical class 0.000 claims description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 11
- 238000002425 crystallisation Methods 0.000 claims description 10
- 230000008025 crystallization Effects 0.000 claims description 10
- 238000001291 vacuum drying Methods 0.000 claims description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 150000002576 ketones Chemical class 0.000 claims description 6
- 150000002825 nitriles Chemical class 0.000 claims description 6
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000002170 ethers Chemical class 0.000 claims description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 4
- 238000001953 recrystallisation Methods 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 2
- MEMUCXUKCBNISQ-UHFFFAOYSA-N acetonitrile;trifluoroborane Chemical compound CC#N.FB(F)F MEMUCXUKCBNISQ-UHFFFAOYSA-N 0.000 claims description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical class CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims description 2
- VWCIBMAHWVHJJM-UHFFFAOYSA-N butyl acetate trifluoroborane Chemical compound C(C)(=O)OCCCC.B(F)(F)F VWCIBMAHWVHJJM-UHFFFAOYSA-N 0.000 claims description 2
- 150000001733 carboxylic acid esters Chemical class 0.000 claims description 2
- JBXYCUKPDAAYAS-UHFFFAOYSA-N methanol;trifluoroborane Chemical compound OC.FB(F)F JBXYCUKPDAAYAS-UHFFFAOYSA-N 0.000 claims description 2
- OYTBOLVDKAGZLT-UHFFFAOYSA-N methyl hydrogen carbonate trifluoroborane Chemical compound COC(O)=O.B(F)(F)F OYTBOLVDKAGZLT-UHFFFAOYSA-N 0.000 claims description 2
- 239000012046 mixed solvent Substances 0.000 claims description 2
- CHNLPLHJUPMEOI-UHFFFAOYSA-N oxolane;trifluoroborane Chemical compound FB(F)F.C1CCOC1 CHNLPLHJUPMEOI-UHFFFAOYSA-N 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 239000000047 product Substances 0.000 abstract description 25
- 238000000034 method Methods 0.000 abstract description 13
- 229910052736 halogen Inorganic materials 0.000 abstract description 5
- 150000002500 ions Chemical class 0.000 abstract description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract description 3
- 239000003792 electrolyte Substances 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 abstract 3
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 52
- 239000000243 solution Substances 0.000 description 38
- 229910052757 nitrogen Inorganic materials 0.000 description 33
- 238000010992 reflux Methods 0.000 description 23
- 239000002904 solvent Substances 0.000 description 18
- 238000010025 steaming Methods 0.000 description 16
- SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical compound CC[N+](C)(CC)CC SEACXNRNJAXIBM-UHFFFAOYSA-N 0.000 description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000007795 chemical reaction product Substances 0.000 description 11
- 239000007789 gas Substances 0.000 description 11
- 238000003756 stirring Methods 0.000 description 9
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 8
- 238000013019 agitation Methods 0.000 description 8
- 229960000935 dehydrated alcohol Drugs 0.000 description 8
- 238000001514 detection method Methods 0.000 description 8
- CXHHBNMLPJOKQD-UHFFFAOYSA-M methyl carbonate Chemical compound COC([O-])=O CXHHBNMLPJOKQD-UHFFFAOYSA-M 0.000 description 8
- 229910001220 stainless steel Inorganic materials 0.000 description 8
- 239000010935 stainless steel Substances 0.000 description 8
- 230000009466 transformation Effects 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 6
- 239000008151 electrolyte solution Substances 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 4
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 3
- 229910052744 lithium Inorganic materials 0.000 description 3
- 239000011255 nonaqueous electrolyte Substances 0.000 description 3
- 150000003527 tetrahydropyrans Chemical class 0.000 description 3
- ONQBOTKLCMXPOF-UHFFFAOYSA-N 1-ethylpyrrolidine Chemical compound CCN1CCCC1 ONQBOTKLCMXPOF-UHFFFAOYSA-N 0.000 description 2
- 238000004607 11B NMR spectroscopy Methods 0.000 description 2
- 238000004293 19F NMR spectroscopy Methods 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- HTLZVHNRZJPSMI-UHFFFAOYSA-N N-ethylpiperidine Chemical compound CCN1CCCCC1 HTLZVHNRZJPSMI-UHFFFAOYSA-N 0.000 description 2
- 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
- 150000001721 carbon Chemical group 0.000 description 2
- 238000012790 confirmation Methods 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000012916 structural analysis Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000002411 thermogravimetry Methods 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
- RILZRCJGXSFXNE-UHFFFAOYSA-N 2-[4-(trifluoromethoxy)phenyl]ethanol Chemical compound OCCC1=CC=C(OC(F)(F)F)C=C1 RILZRCJGXSFXNE-UHFFFAOYSA-N 0.000 description 1
- NEDAUERTDZGLOW-UHFFFAOYSA-N 2-ethyl-1-methylpiperidine Chemical compound CCC1CCCCN1C NEDAUERTDZGLOW-UHFFFAOYSA-N 0.000 description 1
- IDQXZLKEWHBPCA-UHFFFAOYSA-N 2-ethyl-1-methylpyrrolidine Chemical compound CCC1CCCN1C IDQXZLKEWHBPCA-UHFFFAOYSA-N 0.000 description 1
- RDRURTGSFBSIKX-UHFFFAOYSA-N CCN1COCC1 Chemical compound CCN1COCC1 RDRURTGSFBSIKX-UHFFFAOYSA-N 0.000 description 1
- NWORVTSPNLVHSH-UHFFFAOYSA-N CC[N+]1(C)CCOCC1 Chemical compound CC[N+]1(C)CCOCC1 NWORVTSPNLVHSH-UHFFFAOYSA-N 0.000 description 1
- QRNMBYCPVJHTTJ-UHFFFAOYSA-O CC[NH+](C)CCOCC Chemical compound CC[NH+](C)CCOCC QRNMBYCPVJHTTJ-UHFFFAOYSA-O 0.000 description 1
- ZODVEYQCPISNSD-UHFFFAOYSA-N CC[N]1(C)CCOCC1 Chemical compound CC[N]1(C)CCOCC1 ZODVEYQCPISNSD-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000862969 Stella Species 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000001897 boron-11 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- ZUSFORRWERTRDS-UHFFFAOYSA-N chloromethane;n,n-diethylethanamine Chemical compound ClC.CCN(CC)CC ZUSFORRWERTRDS-UHFFFAOYSA-N 0.000 description 1
- 230000009194 climbing Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000007033 dehydrochlorination reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 1
- BDUPRNVPXOHWIL-UHFFFAOYSA-N dimethyl sulfite Chemical compound COS(=O)OC BDUPRNVPXOHWIL-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000005518 electrochemistry Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 229960004756 ethanol Drugs 0.000 description 1
- 238000000806 fluorine-19 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000002555 ionophore Substances 0.000 description 1
- 230000000236 ionophoric effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- QFUDHWDUKUCCHZ-UHFFFAOYSA-N methyl hydrogen sulfite Chemical compound COS(O)=O QFUDHWDUKUCCHZ-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000007773 negative electrode material Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000003880 polar aprotic solvent Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000007774 positive electrode material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- YMBCJWGVCUEGHA-UHFFFAOYSA-M tetraethylammonium chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC YMBCJWGVCUEGHA-UHFFFAOYSA-M 0.000 description 1
- 238000001757 thermogravimetry curve Methods 0.000 description 1
- FNBGFZLKGXGECX-UHFFFAOYSA-M triethyl(methyl)azanium;formate Chemical compound [O-]C=O.CC[N+](C)(CC)CC FNBGFZLKGXGECX-UHFFFAOYSA-M 0.000 description 1
- 238000004758 underpotential deposition Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/14—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups
- C07C209/20—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups with formation of quaternary ammonium compounds
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/54—Electrolytes
- H01G11/58—Liquid electrolytes
- H01G11/62—Liquid electrolytes characterised by the solute, e.g. salts, anions or cations therein
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/13—Energy storage using capacitors
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
Description
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2009100415530A CN101987824B (zh) | 2009-07-31 | 2009-07-31 | 超级电容器用高纯度导电盐的制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2009100415530A CN101987824B (zh) | 2009-07-31 | 2009-07-31 | 超级电容器用高纯度导电盐的制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101987824A CN101987824A (zh) | 2011-03-23 |
CN101987824B true CN101987824B (zh) | 2013-07-03 |
Family
ID=43744639
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2009100415530A Active CN101987824B (zh) | 2009-07-31 | 2009-07-31 | 超级电容器用高纯度导电盐的制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101987824B (zh) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104576081B (zh) * | 2013-10-24 | 2017-11-14 | 中国科学院长春应用化学研究所 | 防凝固型电解液及超级电容器 |
CN104650095B (zh) * | 2015-02-16 | 2017-06-06 | 衢州康鹏化学有限公司 | 一种四氟硼酸螺环季铵盐的制备方法 |
CN106810499A (zh) * | 2016-11-28 | 2017-06-09 | 佛山市尚好门窗有限责任公司 | 一种离子液体及其制备方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1762979A (zh) * | 2005-09-26 | 2006-04-26 | 陈耀华 | 一种四乙基四氟硼酸铵的制备方法 |
CN101131897A (zh) * | 2006-08-21 | 2008-02-27 | 深圳市新宙邦电子材料科技有限公司 | 铝电解电容器、超级电容器用季铵盐的制备方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101006046A (zh) * | 2004-08-24 | 2007-07-25 | 巴斯福股份公司 | 制备高纯度季铵化合物的方法 |
-
2009
- 2009-07-31 CN CN2009100415530A patent/CN101987824B/zh active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1762979A (zh) * | 2005-09-26 | 2006-04-26 | 陈耀华 | 一种四乙基四氟硼酸铵的制备方法 |
CN101131897A (zh) * | 2006-08-21 | 2008-02-27 | 深圳市新宙邦电子材料科技有限公司 | 铝电解电容器、超级电容器用季铵盐的制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN101987824A (zh) | 2011-03-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1837333B1 (en) | Quaternary ammonium salt, electrolyte, electrolyte solution and electrochemical device | |
JP5279764B2 (ja) | 第4級アンモニウム塩およびその製造方法 | |
EP2062902B1 (en) | Lithium salt | |
EP1698631A1 (en) | Ionic liquid, method for producing same, double layer capacitor comprising same, and lithium battery | |
US5750730A (en) | Fluorine-containing dioxolane compound, electrolytic solution composition, battery and capacitor | |
JP4548592B2 (ja) | 電気二重層キャパシタ | |
US20150303511A1 (en) | Functionalized choline chloride ionic liquid, preparation method thereof and use in electrochemical energy storage device | |
JP4913864B2 (ja) | 電解質、これを用いた電解液及び電気化学素子 | |
EP2203247B1 (en) | Organsilicon amine-based electrolytes for use in electrochemical double-layer capacitors | |
WO2006077895A1 (ja) | 第4級アンモニウム塩、電解質、電解液並びに電気化学デバイス | |
JP4929766B2 (ja) | 電解液 | |
CN101987824B (zh) | 超级电容器用高纯度导电盐的制备方法 | |
JP5101260B2 (ja) | 第4級アンモニウム塩電解質を用いた電解液および電気化学素子 | |
KR102638391B1 (ko) | 다이알칸설포닐 아이소소바이드 화합물의 제조 방법, 리튬이차전지용 전해액 첨가제, 리튬이차전지용 전해액 및 리튬이차전지 | |
CN113632285B (zh) | 电解液用添加剂 | |
CN116589433A (zh) | 一种六元环季铵盐及其制备方法和应用 | |
KR20190086147A (ko) | 이미다졸륨 양이온을 이용한 오늄염 화합물을 포함하는 고체전해질 합성용 용매 및 이를 이용한 고체전해질의 합성방법 | |
JPWO2006090657A1 (ja) | 四フッ化ホウ素塩の製造方法、該方法により得られる四フッ化ホウ素塩、これを用いる電気二重層キャパシタ用電解液およびその製造方法 | |
JP2008270643A (ja) | 第4級アンモニウム塩電解質とそれを用いた電解液および電気化学素子 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
ASS | Succession or assignment of patent right |
Owner name: YUEYANG KAIMEN TECHNOLOGY CO., LTD. Free format text: FORMER OWNER: WUHAN CHEMCHEMICAL CO., LTD. Effective date: 20130502 Free format text: FORMER OWNER: GUANGZHOU KAIMEN FINE CHEMICALS CO., LTD. Effective date: 20130502 |
|
C41 | Transfer of patent application or patent right or utility model | ||
COR | Change of bibliographic data |
Free format text: CORRECT: ADDRESS; FROM: 430074 WUHAN, HUBEI PROVINCE TO: 414000 YUEYANG, HUNAN PROVINCE |
|
TA01 | Transfer of patent application right |
Effective date of registration: 20130502 Address after: 414000 Lingang New Industrial District, Yueyang, Hunan, Chenglingji Applicant after: Yueyang Kaimen Technology Co., Ltd. Address before: 430074 room 7-5, building 6218, Kanto Industrial Park, East Lake New Technology Development Zone, Hubei, Wuhan Applicant before: Wuhan Chemchemical Co., Ltd. Applicant before: Guangzhou Kaimen Fine Chemicals Co., Ltd. |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant |