CN109957060A - A kind of high molecular polymer, preparation method and the electrolyte comprising it - Google Patents
A kind of high molecular polymer, preparation method and the electrolyte comprising it Download PDFInfo
- Publication number
- CN109957060A CN109957060A CN201711373103.2A CN201711373103A CN109957060A CN 109957060 A CN109957060 A CN 109957060A CN 201711373103 A CN201711373103 A CN 201711373103A CN 109957060 A CN109957060 A CN 109957060A
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- Prior art keywords
- electrolyte
- acid
- ammonium
- high molecular
- molecular polymer
- Prior art date
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- 239000003792 electrolyte Substances 0.000 title claims abstract description 55
- 229920000642 polymer Polymers 0.000 title claims abstract description 22
- 238000002360 preparation method Methods 0.000 title claims abstract description 21
- 150000003863 ammonium salts Chemical class 0.000 claims abstract description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000178 monomer Substances 0.000 claims abstract description 6
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims abstract description 5
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 claims abstract description 5
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims abstract description 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims abstract description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 60
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 37
- -1 polypropylene Polymers 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 11
- 229910052782 aluminium Inorganic materials 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 11
- JKTYGPATCNUWKN-UHFFFAOYSA-N 4-nitrobenzyl alcohol Chemical compound OCC1=CC=C([N+]([O-])=O)C=C1 JKTYGPATCNUWKN-UHFFFAOYSA-N 0.000 claims description 9
- GJYJYFHBOBUTBY-UHFFFAOYSA-N alpha-camphorene Chemical compound CC(C)=CCCC(=C)C1CCC(CCC=C(C)C)=CC1 GJYJYFHBOBUTBY-UHFFFAOYSA-N 0.000 claims description 9
- 239000004411 aluminium Substances 0.000 claims description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- 229920001451 polypropylene glycol Polymers 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000003999 initiator Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 4
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims description 4
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 claims description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 4
- CFBYEGUGFPZCNF-UHFFFAOYSA-N 2-nitroanisole Chemical compound COC1=CC=CC=C1[N+]([O-])=O CFBYEGUGFPZCNF-UHFFFAOYSA-N 0.000 claims description 4
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims description 4
- 239000000194 fatty acid Substances 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- 150000004665 fatty acids Chemical class 0.000 claims description 4
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- 239000004327 boric acid Substances 0.000 claims description 3
- 229920000344 molecularly imprinted polymer Polymers 0.000 claims description 3
- 229920000137 polyphosphoric acid Polymers 0.000 claims description 3
- 239000011541 reaction mixture Substances 0.000 claims description 3
- 230000004044 response Effects 0.000 claims description 3
- 230000002459 sustained effect Effects 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 229940005561 1,4-benzoquinone Drugs 0.000 claims description 2
- CRWNQZTZTZWPOF-UHFFFAOYSA-N 2-methyl-4-phenylpyridine Chemical compound C1=NC(C)=CC(C=2C=CC=CC=2)=C1 CRWNQZTZTZWPOF-UHFFFAOYSA-N 0.000 claims description 2
- OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 claims description 2
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 claims description 2
- 239000004254 Ammonium phosphate Substances 0.000 claims description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 229930195725 Mannitol Natural products 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 2
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 claims description 2
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 claims description 2
- 229910000148 ammonium phosphate Inorganic materials 0.000 claims description 2
- 235000019289 ammonium phosphates Nutrition 0.000 claims description 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 2
- 235000011187 glycerol Nutrition 0.000 claims description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 2
- 239000000594 mannitol Substances 0.000 claims description 2
- 235000010355 mannitol Nutrition 0.000 claims description 2
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 2
- 235000019837 monoammonium phosphate Nutrition 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 230000001376 precipitating effect Effects 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 2
- 239000000811 xylitol Substances 0.000 claims description 2
- 235000010447 xylitol Nutrition 0.000 claims description 2
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 2
- 229960002675 xylitol Drugs 0.000 claims description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims 2
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 claims 1
- 239000004743 Polypropylene Substances 0.000 claims 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims 1
- 229930006000 Sucrose Natural products 0.000 claims 1
- NDGSBJSAXJUQTE-UHFFFAOYSA-N azane;phosphorous acid Chemical compound N.OP(O)O NDGSBJSAXJUQTE-UHFFFAOYSA-N 0.000 claims 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229920001155 polypropylene Polymers 0.000 claims 1
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 claims 1
- 239000005720 sucrose Substances 0.000 claims 1
- 239000003990 capacitor Substances 0.000 abstract description 24
- 238000000034 method Methods 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 6
- 239000000908 ammonium hydroxide Substances 0.000 description 6
- 238000004321 preservation Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HASSHEPJCMLNQT-UHFFFAOYSA-N boric acid propane-1,1-diol Chemical compound C(CC)(O)O.B(O)(O)O HASSHEPJCMLNQT-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical group N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 1
- RTZZCYNQPHTPPL-UHFFFAOYSA-N 3-nitrophenol Chemical compound OC1=CC=CC([N+]([O-])=O)=C1 RTZZCYNQPHTPPL-UHFFFAOYSA-N 0.000 description 1
- 239000004114 Ammonium polyphosphate Substances 0.000 description 1
- 241000208340 Araliaceae Species 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- JDRJCBXXDRYVJC-UHFFFAOYSA-N OP(O)O.N.N.N Chemical compound OP(O)O.N.N.N JDRJCBXXDRYVJC-UHFFFAOYSA-N 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 159000000013 aluminium salts Chemical class 0.000 description 1
- 229910000329 aluminium sulfate Inorganic materials 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 1
- 229920001276 ammonium polyphosphate Polymers 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229940067597 azelate Drugs 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229910052729 chemical element Inorganic materials 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000005067 remediation Methods 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F216/12—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
- C08F216/14—Monomers containing only one unsaturated aliphatic radical
- C08F216/16—Monomers containing no hetero atoms other than the ether oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/20—Esters of polyhydric alcohols or phenols, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
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- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
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Abstract
The present invention provides a kind of high molecular polymer, preparation method and the electrolyte comprising it;Shown in the high molecular polymer such as formula (I), it is polymerized by monomer undecenoic acid, methyl methacrylate, methacrylic acid, hydroxyethyl methacrylate and vinyl butyl ether;The electrolyte is using the ammonium salt of high molecular polymer shown in formula (I) as main solute, it is compared in similar capacitor product, flash over voltage using the capacitor of electrolyte of the present invention preparation is higher (>=700V), conductivity is more preferable, conductivity variations are significantly smaller after high temperature long-play, and high-temperature stability is more preferable.
Description
Technical field
The present invention relates to technical field of electrolyte, in particular to a kind of high molecular polymer and its aluminium electrolutic capacitor electricity
Solve the application in liquid.
Background technique
Aluminium electrolutic capacitor is base components irreplaceable in various electronic products, with the development of science and technology, society needs
The raising wanted, the requirement for aluminium electrolutic capacitor is higher and higher, make capacitor it is urgent towards small size, long-life, resistance to height
The main flow direction development of warm, high voltage withstanding, high frequency tolerant ripple current, Low ESR, low-leakage current.
And cathode of the electrolyte as aluminium electrolutic capacitor, there is the important work for providing oxonium ion, repairing anode oxide film
With, and determine the operating temperature range, voltage rating, fissipation factor, impedance, rated ripple current, work longevity of capacitor
Life etc., directly affects the performance of capacitor.
Electrolyte composition is complicated, and the main solute and additive up to ten being related to is several.Current main solute is confined to 40
Long-chain polybasic carboxylic acid within carbon, improve the operating temperature range of capacitor, voltage rating, in terms of grow up
It is limited.
In recent years, branched carboxylic acids salt due to side-chain radical steric hindrance effect and alkoxy grp polarization, relatively
There is higher solvability and stronger chemical remediation ability for linear carboxylate, so that aluminium electrolutic capacitor is with low
The advantages that effective impedance, the electric current of resistance to big ripple, thus be widely used.But although branched carboxylic acids salt has than linear carboxylate
More advantages, but there are many problems, during prolonged use, each component of electrolyte can occur slowly
Chemical change causes phenomena such as reducing such as moisture content increase, conductivity reduction and flash over voltage.With the correlation ginseng of capacitor
Number sharply deteriorates, and ultimately causes capacitor failure, reliability is unable to get guarantee.
Therefore, increase main solute main chain segment length, increase the carboxylic-acid functional number for having branch on ortho position, increase main solute
Dissolubility in the electrolytic solution, while the functional group for reducing capacitor main solute in long-time use process to the greatest extent decomposes, acyl
Amination or esterification are then particularly important.As Chinese patent CN106449113 discloses a kind of aluminium electrolutic capacitor thermosetting
Change gel state electrolyte, and specifically disclose the process for preparation of solution system II, using acrylic acid, methacrylate and over cure
Sour ammonium reaction;But solution system II is only the part composition of heat cure gel state electrolyte, the preparation of this kind of electrolyte includes
Multiple steps, and the performance parameter of any solution system II He the heat cure gel state electrolyte are not recorded in specification.
Summary of the invention
The object of the present invention is to provide a kind of novel super-pressure aluminum electrolytic capacitor electrolytes to use main electrolyte, and mentions
It is the corresponding super-pressure aluminum electrolytic capacitor electrolyte being adapted to when main solute for this electrolyte, not only performance is obvious for the electrolyte
Better than the similar-type products sold on the market, cost is lower than similar product, and can satisfy ultra-high voltage aluminum electrolytic capacitor
Requirement.
In order to achieve the above object, one aspect of the present invention provides a kind of high molecular polymer, structure is shown in formula (I):
Wherein, the molecular weight ranges of the high molecular polymer are 10000~100000.
Another aspect of the present invention provides the preparation method of high molecular polymer shown in formula (I), comprising the following steps:
1) reaction monomers undecenoic acid, methyl methacrylate, methacrylic acid, methacrylic acid are added into reaction flask
Hydroxyl ethyl ester and vinyl butyl ether, while initiator and solvent is added;It stirs evenly, is then transferred in oil bath at room temperature
It is warming up to 60-85 DEG C of sustained response 8-24h;
2) reaction mixture after reaction, is poured into water precipitating, then filters, wash, is dry, obtaining formula (I) institute
Show high molecular polymer.
Further, in terms of mass parts, the reaction monomers are 5~20 parts, and the initiator is 0.1~1.0 part, described
Solvent is 80~85 parts.
Further, the reaction monomers undecenoic acid, methyl methacrylate, methacrylic acid, hydroxyethyl methacrylate
The molar ratio of ethyl ester and vinyl butyl ether is 1:0.8~1.2:0.3~0.8:0.8~1.5:1.5~2.5.
Further, the initiator is azodiisobutyronitrile or benzoyl peroxide.
Further, the solvent is tetrahydrofuran, n,N-Dimethylformamide, ethyl acetate, anhydrous methanol, 1
Six ring of oxygen, acetone or acetonitrile.In some embodiments, the solvent is n,N-Dimethylformamide.
The present invention also provides a kind of electrolyte, including main solute, main solvent, secondary solvent and other additives, wherein
The main solute is the ammonium salt of high molecular polymer shown in formula (I).
In some of embodiments, weight percentage of each component in the electrolyte are as follows:
Wherein, the sum of weight percentage of each component is equal to 100%.
In some of embodiments, weight percentage of each component in the electrolyte are as follows:
Wherein, the sum of weight percentage of each component is equal to 100%.
In some of embodiments, weight percentage of each component in the electrolyte are as follows:
Wherein, the sum of weight percentage of each component is equal to 100%.
Further, the main solvent is ethylene glycol.
Further, the secondary solvent is selected from ethylene glycol, diglycol, ethylene glycol monobutyl ether, diethylene glycol (DEG), the third two
Alcohol, glycerine, n-butanol, n-octyl alcohol, diethylene glycol monobutyl ether, diethylene glycol dibutyl ether, diethylene glycol monomethyl ether, diethylene glycol methyl ether, two
Glycol diethyl ether, gamma-butyrolacton, one of polyethylene glycol, butyl acetate or at least two combination.
Further, other described additives mainly include flash over voltage elevator, disappear hydrogen agent or waterproof mixture;That is, its
His additive can be flash over voltage elevator, the hydrogen agent that disappears, in waterproof mixture any one, two or three of combination.
Wherein, the flash over voltage elevator is selected from polyvinyl alcohol, the ammonium polyacrylate, polycyclic of the degree of polymerization 300~2400
Oxidative ethane polypropylene oxide, nano silica, polymerized fatty acid, polymerized fatty acid ammonium, polyethylene glycol 400-20000, poly- third
One of glycol, POLYPROPYLENE GLYCOL or at least two combination.
The hydrogen agent that disappears is selected from p-nitrophenol, metanitrophenol, paranitrobenzoic acid, inclined nitro acetyl acid, isophthalic two
Phenol, hydroquinone, o-Nitroanisole, p nitrobenzyl alcohol, p nitrobenzyl alcohol, ortho-nitroanisole, one in 1,4-benzoquinone
Kind or at least two combination.
The waterproof mixture is selected from boric acid ester compound, phosphate compound, mannitol, D-sorbite, xylitol, sugarcane
Sugar, phosphoric acid, ammonium phosphate, phosphorous acid, ammonium phosphite, ammonium hypophosphite, ammonium hypophosphite, ammonium dihydrogen phosphate, polyphosphoric acid, ammonium polyphosphate
One of salt, alkyl phosphate, silicate compound, aluminium salt or at least two combination.
In some of embodiments, the boric acid ester compound is boric acid propanediol polyester gel.
In some of embodiments, weight percentage of each component in the electrolyte are as follows:
In some of embodiments, weight percentage of each component in the electrolyte are as follows:
In some of embodiments, weight percentage of each component in the electrolyte are as follows:
Aluminium electrolutic capacitor made of electrolyte of the present invention is used the present invention also provides a kind of.
Compared with prior art, the technical effects of the invention are that:
1. high molecular polymer chain length shown in formula (I) is longer and has hydrophilic functional group, can hold onto because long-term
Using and generate a small amount of moisture, increase the service life of product;
2. the synthesis mode of high molecular polymer shown in formula (I) is pure, product purity is high, introduces foreign ion than tradition electricity
It is low to solve matter;
3. compatibility is good in the electrolytic solution for high molecular polymer shown in formula (I), high temperature performance is excellent;
4. being electrolysed using high molecular polymer shown in formula (I) as the electrolyte of main solute than same type super-pressure on the market
Liquid conductivity is high, flash over voltage is high;
5. being assembled into capacitor based on electrolyte of the present invention, the use which meets similar-type products is wanted
It asks, and is had excellent performance in its high temperature storage compared to similar capacitor product.
Term definition
The invention is intended to cover all replacement, modification and equivalent technical solutions, they are included in as claim is fixed
In the scope of the invention of justice.Those skilled in the art will appreciate that many and similar or equivalent method and material of the present invention
Material can be used in the practice present invention.The present invention is not limited to method of the present invention and material.Combined document, patent
With one or more of similar material it is different from the application or in the case where contradicting (term defined in including but not limited to,
Term application, described technology etc.), it is subject to the application.
It will further be appreciated that certain features of the invention, be it is clearly visible, carry out in a number of independent embodiments
Description, but can also provide in combination in a single embodiment.Conversely, various features of the invention, for brevity,
It is described, but can also be provided individually or with any appropriate sub-portfolio in a single embodiment.
Unless otherwise stated, all scientific and technical terminologies used in the present invention have with those skilled in the art of the invention's
It is generally understood identical meaning.All patents of the present invention and public publication are integrally incorporated this hair by reference
It is bright.
Unless otherwise stated, following definition used in the present invention should be applied.For purposes of the present invention, chemical element
With periodic table of elements CAS editions and 1994 the 75th edition " Handbook of Chemistry and Physics " it is consistent.In addition, organic chemistry General Principle can
With reference to " Organic Chemistry ", Thomas Sorrell, University Science Books, Sausalito:
1999, and " March's Advanced Organic Chemistry " by Michael B.Smith and Jerry
Description in March, John Wiley & Sons, New York:2007, entire contents are incorporated by reference into the present invention.
Term "comprising" or " comprising " are open language, that is, include content specified by the present invention, but it is not precluded
Content in terms of him.
Term " room temperature " refers to that temperature range is 25 ± 5 DEG C.
Specific embodiment
As described below is the preferred embodiment of the present invention, and what the present invention was protected is not limited to following preferred implementation side
Formula.It should be pointed out that for those skilled in the art on the basis of the inventive concept, several deformations for making and
It improves, belongs to protection scope of the present invention.
The synthesis of high molecular polymer shown in formula (I) and at salt
Reaction monomers are added into the pear shape bottle of 1000mL: 18.40g undecenoic acid, 10.00g methyl methacrylate,
4.30g methacrylic acid, 13.00g hydroxyethyl methacrylate, 20.00g vinyl butyl ether, while initiator azo is added
Bis-isobutyronitrile 1.314g and solvent N,N-dimethylformamide 260g.Low speed is slowly stirred 30 minutes at room temperature, then by its turn
It moves in oil bath and is warming up to 70 DEG C of sustained response 8h.After reaction, reaction mixture is poured slowly into pure water and is precipitated, mistake
Filter, washing, drying, obtain formula (I) product 43.11g, gross production rate 65.62%.
At salt: obtained formula (I) product being configured to 20% ethylene glycol solution, and logical ammonia is at salt.
1 electrolyte prescription of embodiment and its preparation
Process for preparation: 60% ethylene glycol and 22% gamma-butyrolacton are uniformly mixed at room temperature, increase temperature to 130 DEG C,
1% boric acid propanediol polyester gel is added, heat preservation is cooled to 100 DEG C after 1 hour, opening adjusts moisture, and it is high that 16% formula (I) is added
The ammonium salt of Molecularly Imprinted Polymer adds 0.5% ammonium hypophosphite, 0.5% p nitrobenzyl alcohol, uses ammonium hydroxide after being cooled to room temperature
PH to 5~7 is adjusted, electrolyte is obtained.
1 electrolyte prescription of comparative example and its preparation
Process for preparation: process for preparation: 60% ethylene glycol and 22% gamma-butyrolacton are uniformly mixed at room temperature, increase temperature
1% boric acid propanediol polyester gel is added to 130 DEG C in degree, and heat preservation is cooled to 100 DEG C after 1 hour, opening adjusts moisture, is added
10% alkyl ammonium sebacate, 3%7,9- dimethyl -7,9- benzhydryloxycarbonyl -1,11- dodecanedicarboxylic acid, 3% adipic acid,
0.5% ammonium hypophosphite and 0.5% p nitrobenzyl alcohol are cooled to after room temperature and adjust pH to 5~7 using ammonium hydroxide, be electrolysed
Liquid.
2 electrolyte prescription of embodiment and its preparation
Process for preparation: 65.5% ethylene glycol and 8% ethylene glycol monobutyl ether are uniformly mixed at room temperature, increase temperature extremely
130 DEG C, in 6% polyethylene glycol 2000 is added at this time, heat preservation is cooled to 100 DEG C after 1 hour, opening adjusts moisture, and formula is added
The ammonium salt, 0.4% ammonium hypophosphite and 0.6% p nitrobenzyl alcohol of 19.5% formula (I) high molecular polymer, after being cooled to room temperature
PH to 5~7 is adjusted using ammonium hydroxide, obtains electrolyte.
2 electrolyte prescription of comparative example and its preparation
Process for preparation: 65.5% ethylene glycol and 8% ethylene glycol monobutyl ether are uniformly mixed at room temperature, increase temperature extremely
130 DEG C, 6% polyethylene glycol 2000 is added, heat preservation is cooled to 100 DEG C after 1 hour, opening adjusts moisture, and formula 16%C32 rouge is added
Fat acid, 3.5% ammonium azelate, 0.4% ammonium hypophosphite and 0.6% p nitrobenzyl alcohol use ammonium hydroxide tune after being cooled to room temperature
PH to 5~7 is saved, electrolyte is obtained.
3 electrolyte prescription of embodiment and its preparation
Process for preparation: 66.5% ethylene glycol and 6% diethylene glycol monobutyl ether are uniformly mixed at room temperature, increase temperature extremely
130 DEG C, 5% POLYPROPYLENE GLYCOL is added, heat preservation is cooled to 100 DEG C after 1 hour, opening adjusts moisture, and it is high that 21.5% formula of formula (I) is added
The ammonium salt of Molecularly Imprinted Polymer, 0.3% phosphoric acid and 0.7% o-nitrophenol are cooled to after room temperature and adjust pH to 5~7 using ammonium hydroxide,
Obtain electrolyte.
3 electrolyte prescription of comparative example and its preparation
Process for preparation: 66.5% ethylene glycol and 6% diethylene glycol monobutyl ether are uniformly mixed at room temperature, increase temperature extremely
130 DEG C, 5% POLYPROPYLENE GLYCOL is added, heat preservation is cooled to 100 DEG C after 1 hour, opening adjusts moisture, and formula 17%C34 fat is added
Acid, 4.5% dodecandioic acid ammonium, 0.3% ammonium hypophosphite and 0.7% p nitrobenzyl alcohol use ammonium hydroxide tune after being cooled to room temperature
PH to 5~7 is saved, electrolyte is obtained.
4 performance test of embodiment
Working electrolyte initial performance parameter is as shown in table 1.
Table 1
Number | Moisture (weight %) | Conductivity (30 DEG C, ms/cm) | Flash over voltage (V) |
Embodiment 1 | 1.0 | 0.75 | 740 |
Reference examples 1 | 1.02 | 0.60 | 725 |
Embodiment 2 | 1.02 | 0.48 | 708 |
Reference examples 2 | 1.02 | 0.34 | 685 |
Embodiment 3 | 0.98 | 0.55 | 715 |
Reference examples 3 | 1.00 | 0.33 | 697 |
Using electrolytic capacitor obtained by the electrolyte of the embodiment of the present invention and comparative example after 105 DEG C of high temperature storages, characteristic
And variation is as shown in table 2.
Table 2
Electrolyte and the variation of electrolytic capacitor particular product performance parameters can be found from Tables 1 and 2, compared with comparative example, be adopted
To high molecular polymer shown in formula (I) as the resulting electrolytic capacitor of electrolyte of main solute flash over voltage it is higher (>=
700V), conductivity is more preferable, and after 105 DEG C of hot operation 2000h, conductivity variations are significantly smaller, and high-temperature stability is more preferable.
Claims (10)
1. a kind of high molecular polymer, structure is shown in formula (I):
Wherein, the molecular weight ranges of the high molecular polymer are 10000~100000.
2. a kind of preparation method of high molecular polymer described in claim 1, comprising the following steps:
1) reaction monomers undecenoic acid, methyl methacrylate, methacrylic acid, hydroxyethyl methacrylate second are added into reaction flask
Ester and vinyl butyl ether, while initiator and solvent is added;It stirs evenly at room temperature, is then transferred in oil bath and heats up
To 60-85 DEG C of sustained response 8-24h;
2) reaction mixture after reaction, is poured into water precipitating, then filters, wash, is dry, obtaining height shown in formula (I)
Molecularly Imprinted Polymer.
3. a kind of electrolyte, including main solute, main solvent, secondary solvent and other additives, which is characterized in that the main solute
For the ammonium salt of high molecular polymer shown in formula (I).
4. electrolyte according to claim 3, which is characterized in that weight percentage of each component in the electrolyte are as follows:
Wherein, the sum of weight percentage of each component is equal to 100%.
5. electrolyte according to claim 3, which is characterized in that the main solvent is ethylene glycol.
6. electrolyte according to claim 3, which is characterized in that the secondary solvent is selected from ethylene glycol, a contracting diethyl two
Alcohol, ethylene glycol monobutyl ether, diethylene glycol (DEG), propylene glycol, glycerine, n-butanol, n-octyl alcohol, diethylene glycol monobutyl ether, diethylene glycol dibutyl ether,
One of diethylene glycol monomethyl ether, diethylene glycol methyl ether, diethyl carbitol, gamma-butyrolacton, polyethylene glycol, butyl acetate or extremely
Few two kinds of combination.
7. electrolyte according to claim 3, which is characterized in that other described additives include flash over voltage elevator,
Disappear hydrogen agent or waterproof mixture;Wherein, the flash over voltage elevator is selected from polyvinyl alcohol, the polypropylene of the degree of polymerization 300~2400
Sour ammonium, polyoxyethylene oxypropylene ether, nano silica, polymerized fatty acid, polymerized fatty acid ammonium, polyethylene glycol 400-
20000, one of polypropylene glycol, POLYPROPYLENE GLYCOL or at least two combination;The hydrogen agent that disappears is selected from p-nitrophenol, nitre
Base phenol, paranitrobenzoic acid, inclined nitro acetyl acid, resorcinol, hydroquinone, o-Nitroanisole, p nitrobenzyl alcohol,
One of p nitrobenzyl alcohol, ortho-nitroanisole, 1,4-benzoquinone or at least two combination;The waterproof mixture is selected from boric acid
Ester compounds, phosphate compound, mannitol, D-sorbite, xylitol, sucrose, phosphoric acid, ammonium phosphate, phosphorous acid, phosphorous acid
Ammonium, ammonium hypophosphite, ammonium hypophosphite, ammonium dihydrogen phosphate, polyphosphoric acid, polyphosphoric acid ammonium salt, alkyl phosphate, silicate compound, aluminium
One of salt or at least two combination.
8. according to electrolyte described in claim 3-7 any one, which is characterized in that each component weight hundred in the electrolyte
Divide ratio are as follows:
9. according to electrolyte described in claim 3-7 any one, which is characterized in that each component weight in the super electrolyte
Percentage are as follows:
10. according to electrolyte described in claim 3-7 any one, which is characterized in that each component weight in the super electrolyte
Measure percentage are as follows:
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Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1298180A1 (en) * | 2001-04-13 | 2003-04-02 | Asahi Glass Company Ltd. | Water-and-oil repellant composition |
US20090012235A1 (en) * | 2006-02-03 | 2009-01-08 | Basf Corporation | Dispersant for use in a fluorocarbon coating composition |
CN101599367A (en) * | 2009-07-10 | 2009-12-09 | 南通江海电容器股份有限公司 | 600V ultra-high voltage aluminum working electrolyte of electrolytic capacitor and preparation thereof and application |
CN102863594A (en) * | 2012-09-14 | 2013-01-09 | 苏州飞翔新材料研究院有限公司 | Polymer latex and application thereof |
CN103915258A (en) * | 2014-01-13 | 2014-07-09 | 深圳市智胜新电子技术有限公司 | 650V-700V extra-high-voltage aluminum electrolytic capacitor, working electrolyte and preparation method thereof |
US20140227210A1 (en) * | 2004-06-11 | 2014-08-14 | L'oreal | Gradient copolymer, composition including same and cosmetic make-up or care method |
CN104530299A (en) * | 2014-09-23 | 2015-04-22 | 合肥乐凯科技产业有限公司 | Acrylate emulsion with ester bond structure, preparation method and application thereof |
CN105280385A (en) * | 2014-06-11 | 2016-01-27 | 东莞市东阳光电容器有限公司 | Working electrolyte for slender-type high-voltage aluminum electrolyte capacitors |
US20160168291A1 (en) * | 2013-08-09 | 2016-06-16 | Dow Global Technologies Llc | A hydrophobic alkali soluble emulsion thickener |
CN107256799A (en) * | 2017-07-05 | 2017-10-17 | 东莞市东阳光电容器有限公司 | A kind of electrolyte for aluminum electrolytic capacitor |
-
2017
- 2017-12-19 CN CN201711373103.2A patent/CN109957060B/en active Active
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1298180A1 (en) * | 2001-04-13 | 2003-04-02 | Asahi Glass Company Ltd. | Water-and-oil repellant composition |
US20140227210A1 (en) * | 2004-06-11 | 2014-08-14 | L'oreal | Gradient copolymer, composition including same and cosmetic make-up or care method |
US20090012235A1 (en) * | 2006-02-03 | 2009-01-08 | Basf Corporation | Dispersant for use in a fluorocarbon coating composition |
CN101599367A (en) * | 2009-07-10 | 2009-12-09 | 南通江海电容器股份有限公司 | 600V ultra-high voltage aluminum working electrolyte of electrolytic capacitor and preparation thereof and application |
CN102863594A (en) * | 2012-09-14 | 2013-01-09 | 苏州飞翔新材料研究院有限公司 | Polymer latex and application thereof |
US20160168291A1 (en) * | 2013-08-09 | 2016-06-16 | Dow Global Technologies Llc | A hydrophobic alkali soluble emulsion thickener |
CN103915258A (en) * | 2014-01-13 | 2014-07-09 | 深圳市智胜新电子技术有限公司 | 650V-700V extra-high-voltage aluminum electrolytic capacitor, working electrolyte and preparation method thereof |
CN105280385A (en) * | 2014-06-11 | 2016-01-27 | 东莞市东阳光电容器有限公司 | Working electrolyte for slender-type high-voltage aluminum electrolyte capacitors |
CN104530299A (en) * | 2014-09-23 | 2015-04-22 | 合肥乐凯科技产业有限公司 | Acrylate emulsion with ester bond structure, preparation method and application thereof |
CN107256799A (en) * | 2017-07-05 | 2017-10-17 | 东莞市东阳光电容器有限公司 | A kind of electrolyte for aluminum electrolytic capacitor |
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