WO2013012290A2 - Matériau de couvercle pour batterie et son procédé de fabrication - Google Patents
Matériau de couvercle pour batterie et son procédé de fabrication Download PDFInfo
- Publication number
- WO2013012290A2 WO2013012290A2 PCT/KR2012/005824 KR2012005824W WO2013012290A2 WO 2013012290 A2 WO2013012290 A2 WO 2013012290A2 KR 2012005824 W KR2012005824 W KR 2012005824W WO 2013012290 A2 WO2013012290 A2 WO 2013012290A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- layer
- packaging material
- battery packaging
- aluminum
- barrier layer
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 34
- 238000004519 manufacturing process Methods 0.000 title claims description 16
- 239000000463 material Substances 0.000 title abstract 3
- 239000010410 layer Substances 0.000 claims abstract description 198
- 230000004888 barrier function Effects 0.000 claims abstract description 66
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 64
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 62
- 229910000838 Al alloy Inorganic materials 0.000 claims abstract description 15
- 239000011247 coating layer Substances 0.000 claims abstract description 7
- 239000005022 packaging material Substances 0.000 claims description 60
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 33
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 22
- 238000007743 anodising Methods 0.000 claims description 20
- 239000008151 electrolyte solution Substances 0.000 claims description 19
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 17
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- 235000006408 oxalic acid Nutrition 0.000 claims description 11
- 239000011148 porous material Substances 0.000 claims description 11
- 239000004840 adhesive resin Substances 0.000 claims description 9
- 229920006223 adhesive resin Polymers 0.000 claims description 9
- -1 polyethylene Polymers 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 6
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 claims description 6
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- 229920001225 polyester resin Polymers 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 3
- 239000004327 boric acid Substances 0.000 claims description 3
- 238000009820 dry lamination Methods 0.000 claims description 3
- 238000001125 extrusion Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229920000515 polycarbonate Polymers 0.000 claims description 3
- 239000004417 polycarbonate Substances 0.000 claims description 3
- 239000004645 polyester resin Substances 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 229920006122 polyamide resin Polymers 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 239000004698 Polyethylene Substances 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 239000005060 rubber Substances 0.000 claims 1
- 230000007797 corrosion Effects 0.000 abstract description 25
- 238000005260 corrosion Methods 0.000 abstract description 25
- 230000005611 electricity Effects 0.000 abstract description 3
- 238000007747 plating Methods 0.000 abstract description 3
- 238000009413 insulation Methods 0.000 abstract description 2
- 239000005871 repellent Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 61
- 239000011888 foil Substances 0.000 description 22
- 238000010292 electrical insulation Methods 0.000 description 17
- 238000012360 testing method Methods 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 14
- 239000000126 substance Substances 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 13
- 239000003792 electrolyte Substances 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 12
- 239000000853 adhesive Substances 0.000 description 11
- 230000001070 adhesive effect Effects 0.000 description 11
- 229910052744 lithium Inorganic materials 0.000 description 11
- 229920005672 polyolefin resin Polymers 0.000 description 11
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 10
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 10
- 239000004677 Nylon Substances 0.000 description 9
- 229920001778 nylon Polymers 0.000 description 9
- 238000002048 anodisation reaction Methods 0.000 description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 239000010409 thin film Substances 0.000 description 8
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 6
- 239000000956 alloy Substances 0.000 description 6
- 229910052804 chromium Inorganic materials 0.000 description 6
- 239000011651 chromium Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000003475 lamination Methods 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 229910001416 lithium ion Inorganic materials 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 238000004880 explosion Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- CXHHBNMLPJOKQD-UHFFFAOYSA-M methyl carbonate Chemical compound COC([O-])=O CXHHBNMLPJOKQD-UHFFFAOYSA-M 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229920002943 EPDM rubber Polymers 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 2
- 229920001038 ethylene copolymer Polymers 0.000 description 2
- 238000007765 extrusion coating Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- QPJSUIGXIBEQAC-UHFFFAOYSA-N n-(2,4-dichloro-5-propan-2-yloxyphenyl)acetamide Chemical compound CC(C)OC1=CC(NC(C)=O)=C(Cl)C=C1Cl QPJSUIGXIBEQAC-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000565 sealant Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-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
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical class C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910013870 LiPF 6 Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical group [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229920006121 Polyxylylene adipamide Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000010407 anodic oxide Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000005251 gamma ray Effects 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000002608 ionic liquid Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- QNZFKUWECYSYPS-UHFFFAOYSA-N lead zirconium Chemical compound [Zr].[Pb] QNZFKUWECYSYPS-UHFFFAOYSA-N 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 239000011244 liquid electrolyte Substances 0.000 description 1
- 150000002641 lithium Chemical class 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001690 polydopamine Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007763 reverse roll coating Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/116—Primary casings; Jackets or wrappings characterised by the material
- H01M50/124—Primary casings; Jackets or wrappings characterised by the material having a layered structure
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/116—Primary casings; Jackets or wrappings characterised by the material
- H01M50/124—Primary casings; Jackets or wrappings characterised by the material having a layered structure
- H01M50/126—Primary casings; Jackets or wrappings characterised by the material having a layered structure comprising three or more layers
- H01M50/128—Primary casings; Jackets or wrappings characterised by the material having a layered structure comprising three or more layers with two or more layers of only inorganic material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/116—Primary casings; Jackets or wrappings characterised by the material
- H01M50/117—Inorganic material
- H01M50/119—Metals
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/116—Primary casings; Jackets or wrappings characterised by the material
- H01M50/121—Organic material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/116—Primary casings; Jackets or wrappings characterised by the material
- H01M50/124—Primary casings; Jackets or wrappings characterised by the material having a layered structure
- H01M50/126—Primary casings; Jackets or wrappings characterised by the material having a layered structure comprising three or more layers
- H01M50/129—Primary casings; Jackets or wrappings characterised by the material having a layered structure comprising three or more layers with two or more layers of only organic material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/131—Primary casings; Jackets or wrappings characterised by physical properties, e.g. gas permeability, size or heat resistance
- H01M50/133—Thickness
-
- 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
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention is the outermost layer; A barrier layer comprising aluminum or aluminum alloy foil; And it relates to a battery packaging material including the innermost layer, and more particularly, to provide a battery packaging material and a manufacturing method thereof having an oxide film layer formed on at least one surface of the barrier layer exhibiting a surface resistance of at least O.lkQ / ciif.
- the packaging material has an effect of significantly improving corrosion resistance and electrical insulation while maintaining moisture barrier property.
- lithium ion secondary batteries use a liquid electrolyte
- lithium ion secondary batteries use aluminum cans as packaging materials to prevent leakage of electrolyte and reduce the risk of explosion. Therefore, the lithium ion secondary battery is heavy and bulky due to the aluminum cans used as the packaging material, and even if the aluminum cans are used, the risk of explosion exists because of the use of an ionic liquid electrolyte. This has a low disadvantage. As a result, the company continues to research and develop to further increase energy density while reducing safety and volume.
- Lithium polymer secondary batteries can be pouched to reduce the weight of batteries, thereby reducing production costs and increasing the shape of the batteries. Can be. Since the lithium polymer secondary battery uses a laminate pouch as a packaging material, the lithium polymer secondary battery can be thinned. These polymer batteries, notebooks, It is used in portable terminal devices (mobile phones, PDAs, etc.), video cameras, electric vehicles, energy storage batteries, robots, satellites, etc.
- the structure of a lithium polymer secondary battery having such an advantage is that a laminated aluminum pouch, which is a packaging material, is connected to an electrode terminal (anode: A1, negative electrode: Ni or Cu) which is a metal, and an electrolyte is laminated therein.
- an electrode terminal anode: A1, negative electrode: Ni or Cu
- an electrolyte is laminated therein.
- the internal electrolyte is exposed to moisture, acid and heat are generated by hydrolysis.
- the internal electrolyte may combine with hydrogen to generate strong acidic toxic gas (Gas), causing the battery to explode.
- hydrofluoric acid (HF) in the electrolyte has a high penetration force, and passes through the polypropylene film layer, which is the innermost layer of the pouch, to reach the aluminum thin film layer and dissolve and corrode the aluminum thin film layer surface.
- HF hydrofluoric acid
- the surface of the aluminum thin film layer is treated with a chemical conversion treatment solution and then laminated with a thermoplastic resin to produce a packaging material.
- the packaging material of the lithium polymer secondary battery is a multilayer including a can type formed by processing a metal and a base layer (or outermost layer) / aluminum layer (or barrier layer) / sealant layer (or innermost layer) as basic elements. The thing which produced the film on the pouch is used.
- a general battery packaging material is composed of an outermost layer made of a polyester resin and / or a polyamide resin, an inner layer of a barrier layer made of aluminum or an alloy thereof, or a thermoplastic resin.
- Methyl carbonate (MC), dimethyl carbonate (DMC) and the like are used as the electrolyte of the polymer battery, and an acid such as hydrofluoric acid (HF) is generated by the reaction of the battery. Adhesiveness, moisture barrier, and electrical insulation between the aluminum film and the electrode to prevent lamination are required.
- the barrier layer of the conventional lithium polymer secondary battery is ozone treatment, Attempts have been made to improve physical properties such as adhesion through plasma treatment, gamma ray treatment, heat treatment, or chemical treatment such as chromate or phosphate.
- a technique for improving acid resistance and electrical insulation, in particular, electrical insulation of the barrier layer is disclosed. It is difficult to find.
- a barrier layer of aluminum or aluminum alloy thin film of a "polymer battery by performing the anodization (anodizing) forming a porous aluminum oxide film on the aluminum film, compared to the barrier layer by chromium chemical conversion adhesive It was possible to obtain a battery packaging material that improved the corrosion resistance, electrolytic resistance and electrical insulation while maintaining.
- an object of the present invention is to provide a battery packaging material excellent in acid resistance and electrical insulation.
- Another object of the present invention is to provide a method of manufacturing the battery packaging material.
- aspects of this invention is an outermost layer, containing aluminum or an aluminum alloy, a barrier layer and an innermost layer comprising a, and comprises a porous oxide film layer formed of at least a positive electrode on one surface oxidation treatment (anodizing) of the barrier layer was 0.1 'kffi / cm It relates to a battery packaging material having a surface resistance of two or more.
- One embodiment of the present invention relates to a method for producing a battery packaging material including a porous oxide film by performing anodizing (at least one surface) of the barrier layer.
- the barrier layer in which an oxide film is formed on aluminum is significantly improved in corrosion resistance, electrolytic resistance, and electrical insulation while maintaining adhesiveness as compared to the barrier layer formed by the conventional chemical conversion treatment.
- the specific surface area is properly Adjusted to provide a packaging material with improved adhesion.
- the present invention forms an oxide layer on the aluminum or aluminum alloy as a barrier layer using an anodizing method, while maintaining the moisture barrier property and adhesion of the barrier layer by conventional chemical conversion treatment, There is an effect of dramatically improving the insulation.
- FIG. 1 is a schematic view showing an embodiment of a laminated structure of a battery packaging material having an oxide film layer according to the present invention.
- FIG. 2 is a schematic view showing another embodiment of a laminated structure of a battery packaging material having an oxide film layer according to the present invention.
- FIG. 3 is a schematic view showing still another embodiment of a laminated structure of a battery packaging material having an oxide film layer according to the present invention.
- the battery packaging material includes an outermost layer, a barrier layer and an innermost layer containing aluminum or an aluminum alloy, and includes a porous oxide film layer formed by anodizing on at least one surface of the barrier layer and O
- the present invention relates to a battery packaging material having a surface resistance of .lkQ / oif or more.
- the battery packaging material may be a battery packaging material for a pouch, and is preferably for a lithium polymer secondary battery.
- ' battery packaging material is the outermost layer 10 consisting of a PET layer 11 and a nylon layer 12;
- the innermost layer 18 composed of a barrier layer 13 on which a Crab oxide film layer 14 and a Crab oxide film layer 15 are formed, and a metal adhesive olefin resin layer 18 and a heat adhesive resin layer 19. This sequentially It has a laminated structure. .
- the battery packaging material is the outermost layer 10 consisting of a PET layer 11 and 0-nylon layer 12; It has a structure in which the innermost layer 18 which consists of the barrier layer 13 in which only the 1st oxide film layer 14 was formed, and the metal adhesive olefin resin layer 18 and the heat-adhesive resin layer 19 was sequentially laminated. .
- the battery packaging material is the outermost layer 10 consisting of a PET layer 11 and 0-nylon layer 12; It has a barrier layer 13 in which only the 2nd oxide film layer 15 was formed, the metal adhesive olefin resin layer 18, and a heat adhesive resin layer.
- a porous oxide film having a thickness of 1 to several tens can be formed on the aluminum surface.
- the anodization conditions are adjusted to form the oxide film layers 14 and 16 on one surface or both surfaces of the aluminum constituting the barrier layer to have a surface resistance of at least O.lkQ / oif.
- the oxide layer 14, 16 is porous, 0.2 to 10 / zm, preferably o. m to 5 // m, more preferably 0.5 / ffli to 1 /. If the thickness exceeds 10, it is not preferable because the oxide film tends to be damaged in implementing the continuous process.
- the pore particle diameter of the oxide layer is l, 000 nm or less, for example, Iran to l, 000 nm, more preferably 200 nm or less, for example Iran to 200 nm, in terms of adhesion performance and electrical insulation properties. It can be seen that the corrosion resistance decreases as the unit size and size increase.
- the specific surface area of the oxide film layer is preferably in the range of 0.5 mVg to 100 mVg.
- the specific surface area of the oxide film layer may be selected in an appropriate range in consideration of the improvement of adhesion and the prevention of delamination caused by hydrofluoric acid, electrolyte, and the like.
- the porous oxide film has an improved surface area due to the pores, thereby significantly increasing the adhesion performance between the outermost layer (substrate layer) 10 and the innermost layer 17. In addition, since electrical insulation properties are exhibited, a new performance of electrical insulation can be given to the barrier layer 13.
- the chemical conversion treatment layer formed by the chromatization treatment and the chemical conversion treatment method such as phosphate on the barrier layer does not have electrical insulation. Therefore, when the aluminum surface comes into contact with an electric current, electricity conduction occurs immediately.
- the functionality of the cell pouch can be further improved. For example, when aluminum of the barrier layer is exposed to an electrode or an electrolyte due to damage of the outermost layer (substrate layer) 10 and the innermost layer (silane layer) 17, the performance of the polymer battery is significantly reduced. However, if electrical insulation is provided as in the present invention, higher battery performance can be achieved.
- the outermost layer 10, barrier layer 13 and innermost layer 17 may be composed of all components known in the field of battery packaging materials.
- the outermost layer 10 is used to protect the aluminum thin film used as the barrier layer 13 and to protect against pressure or force from the outside, weather resistance, chemical resistance, formability of the packaging material It is preferable to consist of the polyester-based resin layer 11 and / or the stretched polyamide-based resin layer 12 stretched in the biaxial direction in consideration of the above.
- polyester resin examples include polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyethylene naphthalate (PEN), polybutylene naphthalate (PBN), copolyester, or polycarbonate (PC) film
- PET polyethylene terephthalate
- PBT polybutylene terephthalate
- PEN polyethylene naphthalate
- PBN polybutylene naphthalate
- copolyester or polycarbonate (PC) film
- the biaxially stretched polyamide film resin includes nylon 6, nylon 6.6, a copolymer of nylon 6 and nylon 6.6, nylon 6.10 and polymethacrylylene amidamide (MXD 6), and the like. It may be composed of a single or multiple layers of one or more components selected from the group consisting of.
- MXD 6 polymethacrylylene amidamide
- the barrier layer is a charge for preventing gas and water vapor from penetrating into the lithium battery from the outside, and pinholes and processability of the barrier layer.
- a composite of aluminum or nickel with a thickness of about 15 or more, or an inorganic compound such as silicon oxide or alumina may be added. Can be.
- the barrier layer 13 is preferably a foil of aluminum or aluminum alloy having a thickness of 20 to 80 in consideration of workability.
- the aluminum foil is preferably a 10, 80 alloy-based aluminum foil because the high purity series has excellent processability.
- the aluminum substrate may optionally include silicon, boron, germanium, arsenic, antimony, copper, magnesium, manganese, zinc, lithium, iron, chromium, vanadium, titanium, bismuth, .potassium, tin, lead zirconium, nickel, cobalt and It may be an alloy containing an element selected from the group consisting of a combination thereof.
- the barrier layer 13 is subjected to anodization of aluminum foil to give an electrical insulation function to form porous oxide films 14 and 16.
- the aluminum surface is preferably washed with alkali for the purpose of removing oil. It is a method of changing the surface of aluminum metal into alumina ceramic using electrochemical method. When the method is applied, the aluminum metal itself is oxidized and converted into alumina ceramic, and the surface of the aluminum is stronger than steel and wear resistance is better than that of hard chromium plating. It does not peel off like plating or coating (coating), and the changed alumina ceramic surface has excellent electrical insulation (1500Volt) and electricity flows well inside.
- the anodizing treatment may be used in various ways such as sulfuric acid method, hydroxyl method, chromic acid method, phosphoric acid method or boric acid method.
- the anodization current density of 0.5A / dm 2 to 50A / dm, using an electrolyte solution of from about 10 ° C 'to 35 ° C comprising sulfuric acid, chromic acid, boric acid, dioxane, or in a common acid compound
- the reaction can be made in, and the process can be performed in about 5 seconds to 60 minutes.
- the oxide layer thus treated is a porous oxide (A1 2 0 3 ) layer, which has the inherent function of the barrier layer, and improves electrical insulation, acid resistance, metal adhesion, and wear resistance. '
- the oxide film layers 14 and 16 treated according to the present invention exhibit electrical insulation properties, and firmly adhere the aluminum foil and the olefinic resin layer having metal adhesion to the oxide film layer by hydrofluoric acid generated by hydrolysis of the electrolyte solution and the electrolyte solution.
- the lamination can be prevented while preventing the lamination.
- the innermost layer 17 is polyolefin-based, polycetylene-based, polypropylene-based, polybutylene-based, ethylene copolymer, propylene copolymer, polyester-based, polyamide-based, polycarbonate-based, fluorine-based, silicone-based , Acrylic, ethylene-propylene-diene-monomer rubber (EPDM) and mixtures thereof.
- it is a polyolefin resin layer or the mixed resin layer of polybutadiene and a polyolefin.
- the innermost layer 17 is coextruded without using the barrier layer and the adhesive, and the coextrusion is performed by the extrusion coating method under the conditions of the die and screw temperature in the range of 300 ° C. in the locrc,
- the sealant layer (the innermost layer) can be bonded to the metal without an adhesive in the molten state, and the thickness thereof is preferably between 200 and 200 for reasons of strength reinforcement and interlayer peeling during heat sealing of the battery.
- the innermost layer 17 may be composed of a composite layer using a film such as PET, polyolefin film, nylon, or the like depending on its function.
- a film such as PET, polyolefin film, nylon, or the like depending on its function.
- the metal adhesive olefin resin layer 18 and the heat adhesive resin layer 19 can be formed in multiple layers.
- the metal adhesive olefin resin layer (intermediate layer) 18 is a modified polyolefin resin, and forms a layer containing a mixture of ethylene and modified propylene, modified butadiene, acrylic acid or methacrylic acid, modified acrylic acid, or the like alone or singly. You can.
- the heat adhesive resin layer (the innermost layer) 19 is a lithium battery.
- Low density polyethylene, high density polyethylene, linear low density polyethylene, ethylene copolymers, ethylene-propylene copolymers, polybutadiene, ethylene-butadiene-propylene copolymers, propylene resins and the like may be used alone or in combination.
- a method for manufacturing a battery packaging material including an outermost layer, a barrier layer including an aluminum or aluminum alloy foil, and an innermost layer, wherein anodizing is performed on at least one surface of the barrier layer. It provides a battery packaging material comprising the step of forming an aluminum oxide film.
- the manufacturing method may further include performing dry lamination on one surface and the outermost layer of the barrier layer, and co-extruding the innermost layer on the other surface of the barrier layer.
- the anodizing treatment is to treat the aluminum or aluminum alloy of the barrier layer in an electrolyte solution containing 0.1% to 25% of the acid solution, and the acid of the electrolyte solution which can be used for the anodizing treatment may be sulfuric acid, chromic acid, It may be at least one selected from the group consisting of phosphoric acid, oxalic acid and phosphoric acid, for example, 10-25% sulfuric acid, 0.1-10% oxalic acid, 5-15% phosphoric acid or 2-15% It may be chromic acid, and in the case of using a sulfuric acid solution may be used by adding an additional oxalic acid.
- the anodization treatment is 0.5A / dm ! It can be carried out at 5 seconds to 60 minutes with a current density of from 50 A / dm 2 .
- the temperature of the electrolyte solution is 10 ° C to 35 ° C, more preferably 15 ° C 3 to 3 ( rc, may be a non-uniform thickness of the aluminum oxide filmworm if outside the numerical range and the problem of pore size control.
- the coextrusion has a die and screw temperature of 100 ° C to 300 ° C Under the condition of the innermost layer resin may be carried out by extruding together with the barrier layer in a molten state.
- the outermost layer was composed of PET (about 6) / 0-nylon (about 15), and a soft aluminum foil of 80 alloy series degreasing treatment having a thickness of about 50 mm 3 was used as the barrier layer.
- the aluminum foil was reacted for about 2 minutes at a current density of about lA / dnf using an electrolyte solution of about 20 ° C. in which 0.4% of oxalic acid was added as an additive to sulfuric acid concentration 1, and a thickness of about 0.5 was applied to both sides of aluminum.
- the outermost layer and the barrier layer were laminated by a dry lamination method of injecting a urethane-based adhesive between the two layers, drying them, and bonding each other at a constant temperature and pressure.
- the barrier layer and the innermost layer had a metal adhesive olefin resin layer therebetween, and co-extruded the adhesive resin in a molten state with a high temperature T-die to manufacture a battery packaging material.
- the coextrusion was carried out by an extrusion coating method with a die and screw temperature of about 210 ° C to coat the anodized aluminum oxide film and the heat-adhesive resin layer in-line.
- a mixed resin of modified ethylene and modified propylene was used as the metal adhesive olefin resin layer.
- Example 2 was the same as in Example 1 except that the current density and reaction time were changed to lA / dm 2 and 3 minutes, respectively, to perform anodization, and the thickness of the obtained oxide film was about 0.8im. Was carried out.
- Example 3 is the same as in Example 1 except that the current density and reaction time are changed to lA / dm 2 and 4 minutes, respectively, to perform anodization, and the thickness of the obtained oxide film is about 1 ⁇ . Was carried out.
- Example 4 was carried out in the same manner as in Example 1 except that the current density and reaction time were changed to lA / dm 2 and 20 minutes, respectively, to perform anodization, and the thickness of the obtained oxide film was about 5. It was.
- Example 5 was carried out in the same manner except that the electrolyte solution used in Example 3 was treated with 3% chromic acid instead of the mixed solution of sulfuric acid and oxalic acid.
- Example 6 was carried out in the same manner except that the electrolyte solution used in Example 3 was treated with 10% phosphoric acid instead of the mixed solution of sulfuric acid and oxalic acid.
- Example 7 was carried out in the same manner as in Example 3, except that the electrolyte solution used in Example 3 was treated with oxalic acid of 5> instead of the mixed solution of sulfuric acid and oxalic acid.
- Example 2 The soft aluminum foil of the dealloyed 80 alloy series having a thickness of about 50 used in Example 1 was carried out in the same manner except that aluminum foil without an oxide film was used. Comparative Example 2
- a soft aluminum foil of a dealloyed 80 alloy series having a thickness of about 50iffli used in Example 1 was used as a barrier layer, and a chemical conversion solution was coated on one surface of the barrier layer by a reverse roll coating method (thickness 0. an) and dried (heat treated) at 230 ° C. for 10 seconds to form an anticorrosion layer 120.
- Comparative Example 2 a trivalent chemical conversion film was obtained, and an electrical conduction test of a specimen (5 ⁇ 5 cm) was performed by a current application method, and the results are shown in Table 1 below.
- Adhesion was tested by the peel test method of the innermost layer and aluminum on the specimen (5x5cm) of the battery packaging material according to Examples 1 to 7 and Comparative Examples 1 to 2, the results are shown in Table 2 below.
- Examples 1 to 7 of a battery packaging material including an aluminum oxide film as a barrier layer instead of the chromium chemical conversion layer are used for anodizing treatment. Corrosion does not occur, it can be seen that the resistance to corrosion is improved when used in the battery later.
- Example 10 Instead of the electrolyte solution of 20 ° C used to form the aluminum oxide film on the surface of the aluminum foil in Example 1, using an electrolyte solution of 25 ° C in Example 8 and an electrolyte solution of 30 ° C in Example 9 Except that, substantially the same as in Example 1, the reaction was performed at a current density of about lA / dm 2 for about 2 minutes to form a film of aluminum oxide (A1 2 0 3 ) having a thickness of about 0.5, on both surfaces of the aluminum.
- Aluminum oxide-forming soft aluminum foil was prepared, and a battery packaging material using the same.
- Example 1 When forming an aluminum oxide film on the surface of the aluminum foil in Example 1, to produce an aluminum foil having an aluminum oxide film on the surface in the same manner as in Example 1, except that the voltage was treated with 1.5A / dm, A battery packaging material using the same was prepared.
- Example 1 When forming an aluminum oxide film on the surface of the aluminum foil in Example 1, the aluminum oxide on the surface in the same manner as in Example 1 except that the electrolyte solution was treated with 5% oxalic acid instead of sulfuric acid and oxalic acid mixed solution An aluminum foil having a film was produced, and a battery packaging material using the same was produced.
- an aluminum foil having an aluminum oxide film on its surface was prepared in the same manner as in Example 1 except that the oxide film was used as it was without forming an oxide film on the aluminum alloy-based soft aluminum foil having a thickness of about 50. And the battery packaging material using this was manufactured. ⁇ Test Example 2 >
- the pore sizes of the oxide films prepared according to Examples 1, 8 and 9 were measured by SEM and shown in Table 4.
- An anodizing film was impregnated with 3.5% solution to visually check the salt water test.
- the corrosion degree was measured according to the following criteria, and the results are shown in Table 4 below.
- Example 1 Comparative Example 4 to the porous anodized film (5X5cin) prepared in accordance with the peel test method of the innermost layer and the aluminum (Peel) test method, the results are shown in Table 5 below It was.
- the barrier layer in which an oxide film is formed on aluminum according to the present invention has corrosion resistance, electrolytic resistance, and electrical insulation while maintaining adhesiveness as compared to the barrier layer by conventional chromium chemical conversion treatment.
- the result is a dramatic improvement.
- the corrosion resistance decreases as the unit pore size increases, and the adhesion strength increases as the specific surface area increases. .
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Sealing Battery Cases Or Jackets (AREA)
- Laminated Bodies (AREA)
- Wrappers (AREA)
Abstract
La présente invention propose un matériau de couvercle de type sac pour une batterie, comprenant : une couche la plus à l'extérieur ; une couche barrière comprenant un plaquage en aluminium ou alliage d'aluminium ; et une couche la plus à l'intérieur, une couche de revêtement oxydé étant formée sur au moins une surface de la couche barrière de sorte que la batterie a une résistance de surface d'au moins 0,1 kΩ/cm2. Le matériau de couvercle maintient efficacement une propriété hydrofuge tout en augmentant de manière efficace et significative la durabilité à la corrosion et l'isolation électrique.
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JP2011071127A (ja) * | 2003-04-09 | 2011-04-07 | Nitto Denko Corp | 電池用セパレータのための接着剤担持多孔質フィルムとその利用 |
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JP2011071127A (ja) * | 2003-04-09 | 2011-04-07 | Nitto Denko Corp | 電池用セパレータのための接着剤担持多孔質フィルムとその利用 |
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CN112687996A (zh) * | 2014-09-26 | 2021-04-20 | 大日本印刷株式会社 | 电池用包装材料 |
CN112687996B (zh) * | 2014-09-26 | 2022-11-22 | 大日本印刷株式会社 | 电池用包装材料 |
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