CA1244875A - Method and protected material for making an electrical device - Google Patents
Method and protected material for making an electrical deviceInfo
- Publication number
- CA1244875A CA1244875A CA000466824A CA466824A CA1244875A CA 1244875 A CA1244875 A CA 1244875A CA 000466824 A CA000466824 A CA 000466824A CA 466824 A CA466824 A CA 466824A CA 1244875 A CA1244875 A CA 1244875A
- Authority
- CA
- Canada
- Prior art keywords
- metal
- strip
- protective material
- lithium
- protective
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000463 material Substances 0.000 title claims abstract description 60
- 238000000034 method Methods 0.000 title claims abstract description 24
- 230000001681 protective effect Effects 0.000 claims abstract description 42
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 37
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000007788 liquid Substances 0.000 claims abstract description 17
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
- 229910052751 metal Inorganic materials 0.000 claims description 34
- 239000002184 metal Substances 0.000 claims description 34
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 6
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 2
- 230000002730 additional effect Effects 0.000 claims 1
- 229920006254 polymer film Polymers 0.000 abstract 1
- -1 polyethylene Polymers 0.000 description 19
- 229920000642 polymer Polymers 0.000 description 14
- 239000007772 electrode material Substances 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 8
- 239000010410 layer Substances 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- 238000005096 rolling process Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 238000009833 condensation Methods 0.000 description 5
- 230000005494 condensation Effects 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 230000004224 protection Effects 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 230000001464 adherent effect Effects 0.000 description 3
- 239000000306 component Substances 0.000 description 3
- 239000003792 electrolyte Substances 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 229920006112 polar polymer Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 2
- 229940032159 propylene carbonate Drugs 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 229910013462 LiC104 Inorganic materials 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 239000010405 anode material Substances 0.000 description 1
- 239000010406 cathode material Substances 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical class OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002531 isophthalic acids Chemical class 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- FJXWKBZRTWEWBJ-UHFFFAOYSA-N nonanediamide Chemical compound NC(=O)CCCCCCCC(N)=O FJXWKBZRTWEWBJ-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 229920001197 polyacetylene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000009824 pressure lamination Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 150000003504 terephthalic acids Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000004804 winding Methods 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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
-
- 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
- H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/04—Construction or manufacture in general
- H01M10/0436—Small-sized flat cells or batteries for portable equipment
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/06—Electrodes for primary cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
- H01M4/381—Alkaline or alkaline earth metals elements
- H01M4/382—Lithium
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/624—Electric conductive fillers
- H01M4/625—Carbon or graphite
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/04—Cells with aqueous electrolyte
- H01M6/06—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid
- H01M6/10—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with wound or folded electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
- H01M2004/027—Negative electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M2300/00—Electrolytes
- H01M2300/0002—Aqueous electrolytes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M2300/00—Electrolytes
- H01M2300/0017—Non-aqueous electrolytes
- H01M2300/0025—Organic electrolyte
-
- 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
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Secondary Cells (AREA)
- Primary Cells (AREA)
- Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Control Of Vending Devices And Auxiliary Devices For Vending Devices (AREA)
- Vending Machines For Individual Products (AREA)
- Emergency Protection Circuit Devices (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Bending Of Plates, Rods, And Pipes (AREA)
- Glass Compositions (AREA)
- Inorganic Insulating Materials (AREA)
Abstract
ABSTRACT
METHOD AND PROTECTED MATERIAL FOR
MAKING AN ELECTRICAL DEVICE
A method of making an electrical device, e.g. a lithium cell wherein protective material is removed from a sensitive material (e.g. lithium strip) during, after, or immediately before, incorporating the sensitive material in the device.
The protective material (preferably polymer film) may be peeled off the sensitive material or may be dissolved in liquid, preferably a liquid with which it comes in contact in the device. Articles comprising suitably protected sensitive material and apparatus for making the electrical devices automatically are also disclosed.
METHOD AND PROTECTED MATERIAL FOR
MAKING AN ELECTRICAL DEVICE
A method of making an electrical device, e.g. a lithium cell wherein protective material is removed from a sensitive material (e.g. lithium strip) during, after, or immediately before, incorporating the sensitive material in the device.
The protective material (preferably polymer film) may be peeled off the sensitive material or may be dissolved in liquid, preferably a liquid with which it comes in contact in the device. Articles comprising suitably protected sensitive material and apparatus for making the electrical devices automatically are also disclosed.
Description
~2~ 5 - 1 - RK201.
D R A W I N GS
1 _ S H E E T
METHOD AND PROTECTED MATERIAL FOR
MAKING AN ELECTRICAL DEVICE
This invention relates to a method of makinq electrical devices incorporating sensitive materials, and articles for use in such a method.
Sensitive materials, for example some electrode materials, are sensitive insoEar as they are difficult to handle during manufacture of electrical devices owing to physical weakness or high chemical reactivity, which may necessitate inconvenient handling procedures and~or special conditions such as dry room assembly.
Examples of such sensitive materials include alkali metals and alkaline earth metals, notably lithium metal electrodes for lithium cells~
Lithium metal is difficult to roll into thin strips for use as an electrode, and U.S. Patent No.
3721113 describes a method of alleviating this diffi-culty by rolling the lithium between smooth (surface asperities less than one micron) polymeric surfaces having sufficiently low critical surface tension to prevent adhesion to the lithium. The polymer may be a coating on the surface of rolls used to roll the lithium, or may be in the form of sheeting enclosing or facing the lithium, which does not adhere to the lithium and is peeled off the lithium strip after rolling. While thls method facilitates the rolling : ~.
.
lX~L~875
D R A W I N GS
1 _ S H E E T
METHOD AND PROTECTED MATERIAL FOR
MAKING AN ELECTRICAL DEVICE
This invention relates to a method of makinq electrical devices incorporating sensitive materials, and articles for use in such a method.
Sensitive materials, for example some electrode materials, are sensitive insoEar as they are difficult to handle during manufacture of electrical devices owing to physical weakness or high chemical reactivity, which may necessitate inconvenient handling procedures and~or special conditions such as dry room assembly.
Examples of such sensitive materials include alkali metals and alkaline earth metals, notably lithium metal electrodes for lithium cells~
Lithium metal is difficult to roll into thin strips for use as an electrode, and U.S. Patent No.
3721113 describes a method of alleviating this diffi-culty by rolling the lithium between smooth (surface asperities less than one micron) polymeric surfaces having sufficiently low critical surface tension to prevent adhesion to the lithium. The polymer may be a coating on the surface of rolls used to roll the lithium, or may be in the form of sheeting enclosing or facing the lithium, which does not adhere to the lithium and is peeled off the lithium strip after rolling. While thls method facilitates the rolling : ~.
.
lX~L~875
- 2 - RK201 operation, which produces the thirl lithium strip, it does not improve the efficiency of assembling the delicate lithium strip into electrical devices.
The present invention provides a method of making an electrochemical device which comprises:
(a) melt-extruding a tube of protective material around a strip of alkali or alkaline earth metal which is capable of functioning as an electrode in the device, so as to encapsulate the strip of metal;
(b) deforming the strip of metal while encapsulated by the protective material so as to increase its surface area substantially;
(c) removing the protective material during, after or immediately before incorporating the strip of metal in the device; and (d) incorporating the strip of metal in the device.
This introduction of protected sensitive metal electrode material into the electrochemical device assembly process leads to a number of advantages, especially with regard to automation of hitherto inefficient production processes for electrochemical devices.
It is an advantage of the present invention that the protected strip of metal may be used in a method wherein the protective strip is fed to apparatus which assembles portions of the metal into a plurality of the electrochemical devices.
Preferably the protective material is removed during the feeding of the protected strip to the apparatus, and the apparatus receives a substantially continuous feed of the protected strip and automatically removes the protective material and assembles successive portions of the strip of metal into a succession of the electrochemical devices. The advantages of such an automated process over the piece by-piece hand assembly method~ hitherto used for alkali metal or ~2~8~5
The present invention provides a method of making an electrochemical device which comprises:
(a) melt-extruding a tube of protective material around a strip of alkali or alkaline earth metal which is capable of functioning as an electrode in the device, so as to encapsulate the strip of metal;
(b) deforming the strip of metal while encapsulated by the protective material so as to increase its surface area substantially;
(c) removing the protective material during, after or immediately before incorporating the strip of metal in the device; and (d) incorporating the strip of metal in the device.
This introduction of protected sensitive metal electrode material into the electrochemical device assembly process leads to a number of advantages, especially with regard to automation of hitherto inefficient production processes for electrochemical devices.
It is an advantage of the present invention that the protected strip of metal may be used in a method wherein the protective strip is fed to apparatus which assembles portions of the metal into a plurality of the electrochemical devices.
Preferably the protective material is removed during the feeding of the protected strip to the apparatus, and the apparatus receives a substantially continuous feed of the protected strip and automatically removes the protective material and assembles successive portions of the strip of metal into a succession of the electrochemical devices. The advantages of such an automated process over the piece by-piece hand assembly method~ hitherto used for alkali metal or ~2~8~5
- 3 - RK201 alkaline earth metal electrode materials ~Jill be appreciated.
The protective material may be non-adherent to the metal electrode material, for example in the form of a tube surrounding the strip of the material. However, adherent protective material is preferred.
The method according to this invention can be used to assemble the opposing electrode materials and other com-ponents of the electrochemical device with fewer difficulties than are encountered in handling unprotected electrode materials. The anode or the cathode, or both, of suitable electrochemical devices, for example electrochemical cells, may be provided by way of the method according to this inven-tion, reactive metal anodes, especially lithium anodes, for electrochemical cells being an important practical applica-tion of the invention. The protected strips of metal used may include other components, for example current collector layers, or anti-passivation layers as known per se, adhering to part of the strip of metal e.g. on one major surface of a flat strip electrode. Such a current collector layer, for example, may provide permanent protection to one side of the electrode, with the removable protective material giving it desired temporary protection to the other side.
The protective material may be removed by liquid con-tact, for example contact with a liquid which is incorporated in the device, such as an electrolyte liquid. The protective material may be dissolved by the liquid. Alternatively, the ~, i - ~2D~
The protective material may be non-adherent to the metal electrode material, for example in the form of a tube surrounding the strip of the material. However, adherent protective material is preferred.
The method according to this invention can be used to assemble the opposing electrode materials and other com-ponents of the electrochemical device with fewer difficulties than are encountered in handling unprotected electrode materials. The anode or the cathode, or both, of suitable electrochemical devices, for example electrochemical cells, may be provided by way of the method according to this inven-tion, reactive metal anodes, especially lithium anodes, for electrochemical cells being an important practical applica-tion of the invention. The protected strips of metal used may include other components, for example current collector layers, or anti-passivation layers as known per se, adhering to part of the strip of metal e.g. on one major surface of a flat strip electrode. Such a current collector layer, for example, may provide permanent protection to one side of the electrode, with the removable protective material giving it desired temporary protection to the other side.
The protective material may be removed by liquid con-tact, for example contact with a liquid which is incorporated in the device, such as an electrolyte liquid. The protective material may be dissolved by the liquid. Alternatively, the ~, i - ~2D~
- 4 - RK201 protective material may be a coherent film which is peeled away from the strip of metal.
This invention is useful in relation to sensitive materials such as weak metals, by which is meant metal bodies having a lower tensile strength than an equal thickness of the protective material, especially lithium electrodes for lithium cells. Production of cells (preferably non-aqueous cells) having thin sheet electrodes of these and other materials, e.g., inherently conductive polymers, for example doped polyacetylenes or polypyrroles, or conductively filled polymers, can be facilitated by including the step of deforming the electrode material, for example by rolling, while in contact with the layer of protective material 90 as to decrease the thickness of the electrode material or other-wise alter its form or surface configuration. In this way, devices can be more conveniently assembled from thin sheets of lithium, for example of less than 0.25 millimetres, pre-ferably less than 0.125 millimetres, especially of about 0.075 millimetres thickness, which would otherwise be dif-ficult and expensive to make and assemble into such devices.
It is preferred that the sensitive material be malleable under temperatures and pressure~ which do not unacceptably damage the protective layer. The protective material may also be deformed, e.g. by the rolling operation, in a manner which will assist its subsequent removal from the sensitive material.
~ - ~
37~
_ 5 _ RK201 The invention includes articles comprising the polymer-protected strips of metal in forms especially suited to the method of the invention, for example articles in elongate strip form suitable for feeding to the assembly apparatus;
articles wherein cross-linked organic polymeric protective material is used; articles comprising the other components as aforementioned; articles wherein the protective material has been deformed in a manner which assists its subsequent remo-val; and articles wherein the strip of metal has been deformed as aforementioned. Suitable protective materials include organic materials preferably polymeric materials for example polymers of compounds with polymerizable double bonds and condensation polymers of condensable compounds.
Useful polymers of compounds with polymerizable double bonds may be selected from polymers of ethylenically unsa-turated hydrocarbons having 2 to 12 carbons, such as ethylene propylene, n-hexylene, n-dodecene or 4-tert butylstyrene and of vinyl ethers such as methyl or ethyl vinyl ether.
Preferred among these compounds are polyethylene and polypro-pylene due to their low cost.
Copolymers of the above monomeric compounds are also useful.
Useful condensation polymers may be selected from self-condensates of omega-amino-fatty acids and their lactams, such as condensation polymers from caprolactam and from ll-amino-undecanoic acid.
; .
' ~ :
The condensation polymers can be polyamides of diamines having 6 to 9 carbons and dicarboxylic acids having 6 to 10 carbons. Typical useful diamines include hexamethylene-diamine, nonamethylenediamine and aryldiamines such a m- and p-phenylenediamine. Typical useful dicarboxylic acids include adipic acid, suberic acid, azelaic acid, terephthalic acid and isophthalic acid. The preferred polyamide is the condensate of hexamethylenediamine and adipic acid, for reasons of general availability.
The condensation polymers can also be selected from polyesters of aryldicarboxylic acids such as phthalic, terephthalic and isophthalic acids and glycols having 2 to 6 carbons, such as ethylene, butylene and hexyleneglycols.
Useful solid polymeric compositions include ethylene/chlorotrifluoroethylene copolymers, poly (2-methylpropene), polypropylene, polyethylene, poly (4-tert-butylstyrene), poly(vinyl methyl ether), poly (6-aminocaproic acid), poly(11-aminoundecanoic acid), poly(ethyleneterephthalate), poly(decamethylene sebacamide), poly(heptamethylene pimelamide), poly(octamethylene suberamide), poly(nonamethylene azelaamide) and poly(hexarnethylene adipamide).
In electrochemical cells incorporating substantially non-aqueous polar liquids, the protective material may comprise polymers which are soluble in such liquids, polyethylene oxides being preferred although other polar polymers may be chosen according to their solubility in the liquid actually used ~```, ..
I
~2~4~7~i Liquids in such cell~, for example in lithium cellsJ may for example include various combinations of propylene car-bonate, dimethyl sulphoxide, gamma-butyrolactone, dimethyl formamide, acetonitrile, tetrahydrofuran, 1,2-dimethoxyethane and dioxolane Polyethylene oxides and other polar polymers may also be useful in cells incorporating aqueous liquids.
The protective polymeric materials will preferably be flexible and capable of adhering temporarily to the sensitive material, which may be assisted by suitable surface roughness of the polymer, for example surface asperities greater than one micron in height.
The invention includes the steps of making the protected article by a convenient method, for example by assembling together the strip of metal, and at least one layer of the protective material, either by surrounding the strip of metal with a non-adherent layer of the protective material, Por example by sealing together two strips of the protective material around the strip of metal; or preferably by adhering the protective material to the surface of the strip of metal, for example by melt extru~ion, pressure lamination, or soivent coating. The protective material preferably will not interact with the strip of metal, although beneficial interactions are not excluded from the invention. Cro s-linked protective materials, especially polym0rs cross-linked by ioni~ing radiation, may have beneficial temperature resiqtance and other properties, and may be easier to peel away from the electrode material than uncrosslinked material.
~29L~8~
~ - 8 - RK201 -Examples of the preparation of electrode materials in assembly with the protective polymer layer will now be described to i,llustrate the invention.
Lithium metal (supplied by Foote Mineral Co.) was encap-sulated with polyethylene in a continuous process. Lithium tape, 0.25 millimetres thick and 37 millimetres wide was passed through a crosshead die on a single screw extruder (Baughn 32mm diam screw 25:1 L/D ratio) and a tube oP
polyethylene extruded around the lithium.
The tube was drawn down and laminated with the lithium by passing the lithium plus polyethylene between nip rolls.
The total thickness of the three layered laminate was 0.75 millimetres i.e. 0.25 millimetres polyethylene on either side of the lithium. , ,The polyethylene coating provided protection for lithium against the environment during storage and during rolling to reduce the lithium thickness to 0.075 millimetres prior to use in battery manu-facture. Removal of the protective polymer during assembly into a lithium cell revealed shiny unreacted lithium metal.
This precedure was followed with ~DYNH-3, a low density polyethylene from Union Carbide and ~clair ~405 a linear medium density polyethylene from Du Pont, The laminates were prepared in a dry environment and the cell wa~ assembled in a similar environment.
EXhMPLE 2 Automated cell assembly is demonstrated by feeding a strip of the pro,tected lithium to apparatus illustrated sche-matically in the accompanying drawing.
* Trade Mark ,~.~
~' ' ~2~7~;i - g - RK201 Referring to the drawing, a strip (l) of lithium anode material protected by polymeric protective material according to the invention is fed from a supply roll (2) via feed rolls (3) to stripping rolls (4), where the protective material (5) is taken off onto collector rolls (6), and thence to lay-up rolls (7) where a strip (8) of porous electrode separator material from supply rolls 9 is aligned with each side of the lithium strip. This assembly then passes to lay-up rolls 10 where a strip of cathode material (ll) from feed roll (12) is closely aligned with the lithium anode separator assembly, the separator material previously aligned with the lithium anode being between the anode and the cathode. The aligned andoe/cathode assembly then pro-ceeds to a spool threading unit (13) and thence to a spool winding unit (14) wherein the assembly is coiled or spooled to provide a coiled electrode assembly. The coiled assembly then passes to the spool casing unit (15), where the coiled assembly is sealed in a cell casing together with suitable electrolyte liquid. Suitable practical embodiments of the production equipment thus schematically described can readily be devised, and it will be understood that removal of the protective layer from only one side of the electrode strip is acceptable where the other side carries a coating such as a current collector layer which itself provides adequate pro-tection without an overlying protective layer.
Example ~ was repeated using polyethylene oxide ~WSR
N750 from Union Carbide) in place oP the polyethylene, and the encapsulating polyethylene oxide was removed from a portion of the lithium by dissolving it in a typical electrolyte solution for lithium cells, viz. 1M LiC104 in a 50:50 mixture of 1, 2-dlmethoxyethane and propylene carbonate.
* Trade Mark ~.2~
The encapsulated lithium produced in Example 3 was incorporated in a cell in a manner similar to than described in Example 2, except that the encapsulating polyethylene oxide was not removed at the stripper rolls (4) and was incorporated in the cell for subsequent removal by dissolu-tion in the cell electrolyte liquid.
This invention is useful in relation to sensitive materials such as weak metals, by which is meant metal bodies having a lower tensile strength than an equal thickness of the protective material, especially lithium electrodes for lithium cells. Production of cells (preferably non-aqueous cells) having thin sheet electrodes of these and other materials, e.g., inherently conductive polymers, for example doped polyacetylenes or polypyrroles, or conductively filled polymers, can be facilitated by including the step of deforming the electrode material, for example by rolling, while in contact with the layer of protective material 90 as to decrease the thickness of the electrode material or other-wise alter its form or surface configuration. In this way, devices can be more conveniently assembled from thin sheets of lithium, for example of less than 0.25 millimetres, pre-ferably less than 0.125 millimetres, especially of about 0.075 millimetres thickness, which would otherwise be dif-ficult and expensive to make and assemble into such devices.
It is preferred that the sensitive material be malleable under temperatures and pressure~ which do not unacceptably damage the protective layer. The protective material may also be deformed, e.g. by the rolling operation, in a manner which will assist its subsequent removal from the sensitive material.
~ - ~
37~
_ 5 _ RK201 The invention includes articles comprising the polymer-protected strips of metal in forms especially suited to the method of the invention, for example articles in elongate strip form suitable for feeding to the assembly apparatus;
articles wherein cross-linked organic polymeric protective material is used; articles comprising the other components as aforementioned; articles wherein the protective material has been deformed in a manner which assists its subsequent remo-val; and articles wherein the strip of metal has been deformed as aforementioned. Suitable protective materials include organic materials preferably polymeric materials for example polymers of compounds with polymerizable double bonds and condensation polymers of condensable compounds.
Useful polymers of compounds with polymerizable double bonds may be selected from polymers of ethylenically unsa-turated hydrocarbons having 2 to 12 carbons, such as ethylene propylene, n-hexylene, n-dodecene or 4-tert butylstyrene and of vinyl ethers such as methyl or ethyl vinyl ether.
Preferred among these compounds are polyethylene and polypro-pylene due to their low cost.
Copolymers of the above monomeric compounds are also useful.
Useful condensation polymers may be selected from self-condensates of omega-amino-fatty acids and their lactams, such as condensation polymers from caprolactam and from ll-amino-undecanoic acid.
; .
' ~ :
The condensation polymers can be polyamides of diamines having 6 to 9 carbons and dicarboxylic acids having 6 to 10 carbons. Typical useful diamines include hexamethylene-diamine, nonamethylenediamine and aryldiamines such a m- and p-phenylenediamine. Typical useful dicarboxylic acids include adipic acid, suberic acid, azelaic acid, terephthalic acid and isophthalic acid. The preferred polyamide is the condensate of hexamethylenediamine and adipic acid, for reasons of general availability.
The condensation polymers can also be selected from polyesters of aryldicarboxylic acids such as phthalic, terephthalic and isophthalic acids and glycols having 2 to 6 carbons, such as ethylene, butylene and hexyleneglycols.
Useful solid polymeric compositions include ethylene/chlorotrifluoroethylene copolymers, poly (2-methylpropene), polypropylene, polyethylene, poly (4-tert-butylstyrene), poly(vinyl methyl ether), poly (6-aminocaproic acid), poly(11-aminoundecanoic acid), poly(ethyleneterephthalate), poly(decamethylene sebacamide), poly(heptamethylene pimelamide), poly(octamethylene suberamide), poly(nonamethylene azelaamide) and poly(hexarnethylene adipamide).
In electrochemical cells incorporating substantially non-aqueous polar liquids, the protective material may comprise polymers which are soluble in such liquids, polyethylene oxides being preferred although other polar polymers may be chosen according to their solubility in the liquid actually used ~```, ..
I
~2~4~7~i Liquids in such cell~, for example in lithium cellsJ may for example include various combinations of propylene car-bonate, dimethyl sulphoxide, gamma-butyrolactone, dimethyl formamide, acetonitrile, tetrahydrofuran, 1,2-dimethoxyethane and dioxolane Polyethylene oxides and other polar polymers may also be useful in cells incorporating aqueous liquids.
The protective polymeric materials will preferably be flexible and capable of adhering temporarily to the sensitive material, which may be assisted by suitable surface roughness of the polymer, for example surface asperities greater than one micron in height.
The invention includes the steps of making the protected article by a convenient method, for example by assembling together the strip of metal, and at least one layer of the protective material, either by surrounding the strip of metal with a non-adherent layer of the protective material, Por example by sealing together two strips of the protective material around the strip of metal; or preferably by adhering the protective material to the surface of the strip of metal, for example by melt extru~ion, pressure lamination, or soivent coating. The protective material preferably will not interact with the strip of metal, although beneficial interactions are not excluded from the invention. Cro s-linked protective materials, especially polym0rs cross-linked by ioni~ing radiation, may have beneficial temperature resiqtance and other properties, and may be easier to peel away from the electrode material than uncrosslinked material.
~29L~8~
~ - 8 - RK201 -Examples of the preparation of electrode materials in assembly with the protective polymer layer will now be described to i,llustrate the invention.
Lithium metal (supplied by Foote Mineral Co.) was encap-sulated with polyethylene in a continuous process. Lithium tape, 0.25 millimetres thick and 37 millimetres wide was passed through a crosshead die on a single screw extruder (Baughn 32mm diam screw 25:1 L/D ratio) and a tube oP
polyethylene extruded around the lithium.
The tube was drawn down and laminated with the lithium by passing the lithium plus polyethylene between nip rolls.
The total thickness of the three layered laminate was 0.75 millimetres i.e. 0.25 millimetres polyethylene on either side of the lithium. , ,The polyethylene coating provided protection for lithium against the environment during storage and during rolling to reduce the lithium thickness to 0.075 millimetres prior to use in battery manu-facture. Removal of the protective polymer during assembly into a lithium cell revealed shiny unreacted lithium metal.
This precedure was followed with ~DYNH-3, a low density polyethylene from Union Carbide and ~clair ~405 a linear medium density polyethylene from Du Pont, The laminates were prepared in a dry environment and the cell wa~ assembled in a similar environment.
EXhMPLE 2 Automated cell assembly is demonstrated by feeding a strip of the pro,tected lithium to apparatus illustrated sche-matically in the accompanying drawing.
* Trade Mark ,~.~
~' ' ~2~7~;i - g - RK201 Referring to the drawing, a strip (l) of lithium anode material protected by polymeric protective material according to the invention is fed from a supply roll (2) via feed rolls (3) to stripping rolls (4), where the protective material (5) is taken off onto collector rolls (6), and thence to lay-up rolls (7) where a strip (8) of porous electrode separator material from supply rolls 9 is aligned with each side of the lithium strip. This assembly then passes to lay-up rolls 10 where a strip of cathode material (ll) from feed roll (12) is closely aligned with the lithium anode separator assembly, the separator material previously aligned with the lithium anode being between the anode and the cathode. The aligned andoe/cathode assembly then pro-ceeds to a spool threading unit (13) and thence to a spool winding unit (14) wherein the assembly is coiled or spooled to provide a coiled electrode assembly. The coiled assembly then passes to the spool casing unit (15), where the coiled assembly is sealed in a cell casing together with suitable electrolyte liquid. Suitable practical embodiments of the production equipment thus schematically described can readily be devised, and it will be understood that removal of the protective layer from only one side of the electrode strip is acceptable where the other side carries a coating such as a current collector layer which itself provides adequate pro-tection without an overlying protective layer.
Example ~ was repeated using polyethylene oxide ~WSR
N750 from Union Carbide) in place oP the polyethylene, and the encapsulating polyethylene oxide was removed from a portion of the lithium by dissolving it in a typical electrolyte solution for lithium cells, viz. 1M LiC104 in a 50:50 mixture of 1, 2-dlmethoxyethane and propylene carbonate.
* Trade Mark ~.2~
The encapsulated lithium produced in Example 3 was incorporated in a cell in a manner similar to than described in Example 2, except that the encapsulating polyethylene oxide was not removed at the stripper rolls (4) and was incorporated in the cell for subsequent removal by dissolu-tion in the cell electrolyte liquid.
Claims (9)
1. A method of making an electrochemical device which comprises:
(a) melt-extruding a tube of protective material around a strip of alkali or alkaline earth metal which is capable of functioning as an electrode in the device, so as to encapsulate the strip of metal;
(b) deforming the strip of metal while encap-sulated by the protective material so as to increase its surface area substantially;
(c) removing the protective material during, after or immediately before incorporating the strip of metal in the device; and (d) incorporating the strip of metal in the device.
(a) melt-extruding a tube of protective material around a strip of alkali or alkaline earth metal which is capable of functioning as an electrode in the device, so as to encapsulate the strip of metal;
(b) deforming the strip of metal while encap-sulated by the protective material so as to increase its surface area substantially;
(c) removing the protective material during, after or immediately before incorporating the strip of metal in the device; and (d) incorporating the strip of metal in the device.
2. A method according to claim 1, wherein the strip of metal is fed to apparatus which assembles portions of the strip of metal into a plurality of the electrochemical devi-ces.
3. A method according to claim 2, wherein the protec-tive material is removed during the feeding of the strip of protected metal to the apparatus.
4. A method according to claim 3, wherein the apparatus receives a substantially continuous feed of the strip of pro-tected metal and automatically removes the protective material and assembles successive portions of the metal into a succession of the electrochemical devices.
5. A method according to any of claims 1 to 3, wherein the protective material is removed by contact with liquid.
6. A method according to claim 1, wherein the protec-tive material is removed by contact with liquid incorporated in the device.
7. A method according to claim 6, wherein the liquid is a substantially non-aqueous polar liquid and the protective material comprises polyethylene oxide.
8. A method according to any of claims 1 to 3, wherein the strip of protective metal includes at least one addi-tional material in addition to the strip of metal and the removable protective material, the additional material being capable of functioning as another component of the said electrochemical device.
9. A method according to any of claims 1 to 3, wherein the metal comprises lithium.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8329207 | 1983-11-02 | ||
| GB838329207A GB8329207D0 (en) | 1983-11-02 | 1983-11-02 | Making electrical device |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1244875A true CA1244875A (en) | 1988-11-15 |
Family
ID=10551084
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000466824A Expired CA1244875A (en) | 1983-11-02 | 1984-11-01 | Method and protected material for making an electrical device |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0147929B1 (en) |
| JP (1) | JPS60115168A (en) |
| KR (1) | KR850003822A (en) |
| AT (1) | ATE54039T1 (en) |
| AU (1) | AU575597B2 (en) |
| CA (1) | CA1244875A (en) |
| DE (1) | DE3482565D1 (en) |
| GB (2) | GB8329207D0 (en) |
| IL (1) | IL73397A (en) |
| IN (1) | IN163424B (en) |
| ZA (1) | ZA8408595D (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8407871D0 (en) * | 1984-03-27 | 1984-05-02 | Ici Plc | Electrode and electrolytic cell |
| FR2616970B1 (en) * | 1987-06-18 | 1995-05-19 | Elf Aquitaine | MULTI-LAYERED ASSEMBLY FOR PRODUCING THE ASSEMBLY OF A GENERATOR, METHOD FOR PREPARING THE SAME AND PRODUCING THE COMPLETE GENERATOR, AND GENERATOR THUS PRODUCED |
| FR2616971A1 (en) * | 1987-06-18 | 1988-12-23 | Elf Aquitaine | INTERMEDIATE ASSEMBLY FOR THE PRODUCTION IN THE FORM OF THIN FILMS OF A LITHIUM BATTERY, METHOD OF MAKING SAME, AND METHOD FOR PRODUCING THE ACCUMULATOR |
| JPH04126362A (en) * | 1990-09-18 | 1992-04-27 | Yuasa Corp | Manufacture of sheet-shaped cell |
| CA2059228A1 (en) * | 1992-01-13 | 1993-07-14 | Guy St-Amant | Differential adhesion making process for thin lithium patterns |
| WO2000077875A1 (en) * | 1999-06-11 | 2000-12-21 | Le Carbone Lorraine | Method for making a multilayer structure for lithium polymer generators |
| US6585846B1 (en) * | 2000-11-22 | 2003-07-01 | 3M Innovative Properties Company | Rotary converting apparatus and method for laminated products and packaging |
| CN105489846B (en) * | 2016-01-11 | 2018-03-20 | 宁德时代新能源科技股份有限公司 | Pole piece lithium supplementing method and system |
| FR3118719B1 (en) * | 2021-01-14 | 2023-01-06 | Commissariat Energie Atomique | LITHIUM METAL STRIP ROLLING DEVICE |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1670585A (en) * | 1923-01-05 | 1928-05-22 | Nat Carbon Co Inc | Container for granular depolarizers and process of making the same |
| NL18422C (en) * | 1925-04-08 | 1928-12-15 | ||
| GB532581A (en) * | 1939-07-20 | 1941-01-27 | Burgess Battery Co | Galvanic dry cell |
| BE541308A (en) * | 1954-09-16 | |||
| DE1097961B (en) * | 1958-08-11 | 1961-01-26 | Shell Int Research | Process for the protection of hygroscopic shaped catalyst pieces against moisture by applying a coating to the shaped pieces |
| US3368924A (en) * | 1966-01-28 | 1968-02-13 | Army Usa | Battery with zinc anode coated with alkali metal getter |
| US3508967A (en) * | 1967-09-22 | 1970-04-28 | Gulton Ind Inc | Negative lithium electrode and electrochemical battery containing the same |
| GB1298453A (en) * | 1969-01-02 | 1972-12-06 | Nat Res Dev | Production of polymer films by evaporation |
| US3721113A (en) * | 1971-08-23 | 1973-03-20 | Du Pont | Rolling of lithium |
| BE788686A (en) * | 1971-09-15 | 1973-03-12 | Agfa Gevaert Nv | ISCHE MATERIALEN VERPAKKINGSPAPIER VOOR STRALINGSGEVOELIGE FOTOGRAF |
| US3783666A (en) * | 1971-12-01 | 1974-01-08 | Power Conversion Inc | Apparatus for fabricating lithium anodes |
| DE2459009C3 (en) * | 1974-12-13 | 1980-02-14 | Varta Batterie Ag, 3000 Hannover | Process for drying electrode plates for electrical accumulators |
| DE2546585C3 (en) * | 1975-10-17 | 1981-04-16 | Varta Batterie Ag, 3000 Hannover | Process for the production of galvanic elements with negative electrodes made of lithium or calcium |
| US4056885A (en) * | 1976-12-15 | 1977-11-08 | Exxon Research & Engineering Co. | Method of preparing lithium-aluminum alloy electrodes |
| GB2062344B (en) * | 1979-10-02 | 1983-06-08 | Lucas Industries Ltd | Lead-acid battery plates |
| US4315976A (en) * | 1979-12-21 | 1982-02-16 | Union Carbide Corporation | Coated active anodes |
| GB2081491B (en) * | 1980-08-07 | 1983-08-17 | Chloride Group Ltd | Making battery plates |
| GB2090696A (en) * | 1980-12-29 | 1982-07-14 | Gould Inc | Battery plate manufacture |
| IL73398A (en) * | 1983-11-02 | 1987-10-20 | Raychem Ltd | Protected metal components and their production |
-
1983
- 1983-11-02 GB GB838329207A patent/GB8329207D0/en active Pending
-
1984
- 1984-11-01 IL IL73397A patent/IL73397A/en unknown
- 1984-11-01 DE DE8484307537T patent/DE3482565D1/en not_active Expired - Lifetime
- 1984-11-01 GB GB08427700A patent/GB2151069B/en not_active Expired
- 1984-11-01 JP JP59232247A patent/JPS60115168A/en active Pending
- 1984-11-01 AT AT84307537T patent/ATE54039T1/en not_active IP Right Cessation
- 1984-11-01 CA CA000466824A patent/CA1244875A/en not_active Expired
- 1984-11-01 KR KR1019840006837A patent/KR850003822A/en not_active Withdrawn
- 1984-11-01 EP EP84307537A patent/EP0147929B1/en not_active Expired - Lifetime
- 1984-11-02 ZA ZA19848595D patent/ZA8408595D/en unknown
- 1984-11-02 IN IN825/MAS/84A patent/IN163424B/en unknown
- 1984-11-02 AU AU34962/84A patent/AU575597B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| GB8329207D0 (en) | 1983-12-07 |
| IN163424B (en) | 1988-09-17 |
| EP0147929A1 (en) | 1985-07-10 |
| GB2151069A (en) | 1985-07-10 |
| DE3482565D1 (en) | 1990-07-26 |
| KR850003822A (en) | 1985-06-26 |
| EP0147929B1 (en) | 1990-06-20 |
| IL73397A0 (en) | 1985-02-28 |
| IL73397A (en) | 1987-11-30 |
| AU3496284A (en) | 1985-05-09 |
| AU575597B2 (en) | 1988-08-04 |
| JPS60115168A (en) | 1985-06-21 |
| GB8427700D0 (en) | 1984-12-05 |
| ATE54039T1 (en) | 1990-07-15 |
| ZA8408595D (en) | 1986-07-30 |
| GB2151069B (en) | 1987-10-21 |
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