US425335A - Friedrich marx - Google Patents
Friedrich marx Download PDFInfo
- Publication number
- US425335A US425335A US425335DA US425335A US 425335 A US425335 A US 425335A US 425335D A US425335D A US 425335DA US 425335 A US425335 A US 425335A
- Authority
- US
- United States
- Prior art keywords
- metal
- electrodes
- metals
- marx
- friedrich
- 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 - Lifetime
Links
- 239000002184 metal Substances 0.000 description 58
- 229910052751 metal Inorganic materials 0.000 description 58
- 238000000034 method Methods 0.000 description 38
- 150000002739 metals Chemical class 0.000 description 20
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 16
- 238000003723 Smelting Methods 0.000 description 14
- 238000001556 precipitation Methods 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 12
- 229910052742 iron Inorganic materials 0.000 description 8
- 238000005096 rolling process Methods 0.000 description 8
- 235000002639 sodium chloride Nutrition 0.000 description 8
- 239000011780 sodium chloride Substances 0.000 description 8
- 238000005868 electrolysis reaction Methods 0.000 description 6
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000000151 deposition Methods 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 230000001376 precipitating Effects 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 240000003936 Plumbago auriculata Species 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000003292 diminished Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001590 oxidative Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 230000003245 working Effects 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
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
- H01M4/04—Processes of manufacture in general
- H01M4/0438—Processes of manufacture in general by electrochemical processing
-
- 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 current generated by the battery will be much stronger than those batteries in which the metal employed has been obtained by the smelting process, for the reason that the electrolyte can combine more thoroughly with the electrodes, and thus the chemical reaction will take place more vigorously.
- a further modification which may be advantageously employed in the practice consists in depositing the metal which is to form the electrode directly on a conductor, (metal plate,) to which it is fixed by rolling after having been washed as above described.
- the mechanical treatment is of importance in so far as by this means the electrode becomes capable of resistance to a certain extent, and
- quicksilver which is accomplished by adding a soluble quicksilver salt to the electric bath in the one case or by adding metallic quicksilver to the precipitated metal.
- the gist of the present invention consists in avoiding the smelting process entirely and to use the loose chemically-active metal after having been Worked directly as an electrode.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Cell Electrode Carriers And Collectors (AREA)
Description
UNITED STATES ATENT nricn.
FRIEDRICH MARX, OF BERLIN, GERMANY.
PROCESS OF MANUFACTURING METALLIC ELECTRODES FOR BATTERlES.
SPECIFICATION forming part of Letters Patent No. 425,335, dated April 8, 1890. Application filed December 30, 1889. Serial No. 335,422. (No model.)
To a whom, it may concern:
Be it known that I, FRIEDRICH MARX, a subject of the King of Prussia, German Emperor, and a resident of Berlin, No. 91 Grossbeeren Strasse, in the Kingdom of Prussia, German Empire, have invented a certain new and useful Process of hlanufacturing Metallic Electrodes, of which the following is an exact description, and for which I have applied for Letters Patent in Germany on the 21st of November, 1889.
The method of manufacturing metallic .electrodes in use up till now consisted in working into the required form the metal obtained by a smelting process and then placing the same into the battery.
I have observed that the working effect of metallic electrodes may be considerably increased by avoiding the smelting process in their manufacture, and, instead, depositing the metal by electrolysis or precipitation by other metals in a loose state. I base my process on the fact that the metals gained in the smelting process, on account. of their mechanical compactness and dense molecular combination, are capable of resisting chemical actions to a considerable extent, and consequently the electrolyte can only operate slowly on the same. If, on the other hand, the metal for the electrode be obtained by precipitation with other metals or electrolysis, a loose mass, almost of a spongy nature, is gained, which is easily attacked by chemical reagents. If, now, the metal gained by electrolysis or precipitation with other metals be used as electrodes for galvanic batteries, the current generated by the battery will be much stronger than those batteries in which the metal employed has been obtained by the smelting process, for the reason that the electrolyte can combine more thoroughly with the electrodes, and thus the chemical reaction will take place more vigorously.
Of course the decomposition of a certain amount of metal will only produce the corresponding amount of electricity, so that the sum of the amount of-electricity generated remains the same in both cases, whether the electrodes are made of metal obtained by the smelting or electrolytical process or that of precipitation by other metals. The advantage of the presentinvcution,however, is that electrodes of metal gained by the latter process, on account of the increased energy of the chemical reaction, will be used up or decomposed in much shorter time, so that the batteries need not to be so large as was formerly necessary, while the strength of the current does not get less.
It need hardly be mentioned that the electrodes must be renewed more often.
For the practical application of my invention I proceed in the following manner: The porous loose mass of metal gained by the electrolytic process or by precipitation with other metals is first carefully washed to clean it of any salts which it may contain and to prevent later oxidation. The metal is then either rolled or hammered to a concrete mass, which may then be coated with plumbago or metallic oxides in order to exclude the oxygen of the air. It is often advantageous to roll into the mass a woveu-wire fabric or rough metal plate, which, if necessary, may be used to carry the connection binder.
A further modification which may be advantageously employed in the practice consists in depositing the metal which is to form the electrode directly on a conductor, (metal plate,) to which it is fixed by rolling after having been washed as above described. The mechanical treatment is of importance in so far as by this means the electrode becomes capable of resistance to a certain extent, and
then again the oxidizing effect of the air is.
diminished, because the surface of the metal will be made denser by the mechanical pressure.
In the case of zinc it is advantageous to add quicksilver, which is accomplished by adding a soluble quicksilver salt to the electric bath in the one case or by adding metallic quicksilver to the precipitated metal.
As an example, showing how much stronger electrodes manufactured on this principle work, it may be mentioned that an ordinary battery of iron and carbon in a solution of common salt gave the following result: 0.1 ampere and 0.35 volt, (the iron having been gained by the smelting process,) while a battery of the same size in which the iron was gainedby electrolytic process and then worked mechanically gave the result: 0.9 am pore and 0.85 volt;
I am aware that metals gained by the electrolytic process have been Worked up for electrodes; but this was always achieved by first melting, then casting and rolling the same into the required form. The gist of the present invention consists in avoiding the smelting process entirely and to use the loose chemically-active metal after having been Worked directly as an electrode.
The process above described may be employed for every sort of metal Which has up till now been used for electrodes; but practice has proved that the manufacture of zinc, iron, and copper electrodes maybe conducted on my principle with particular advantage.
Having thus fully described and ascertained the nature of my said invention, What I desire to secure by Letters Patent of the United States is 1. The process of manufacturing metallic electrodes for galvanic batteries by purifying from the presence of salts the metallic deposit obtained by the electrolytic process or by precipitation With other metals andthen working mechanically the mass so purified into the required form, substantially as specified. 2. The process of manufacturing metallic electrodes for galvanic batteries by purifying from the presence of salts the metallic deposit obtained by the electrolytic process or by precipitation with other metals and then rolling into the mass so purified a wire Woven fabric or metal plate, in the manner substantially as described. I
8. The process of manufacturing metallic electrodes for galvanic batteries by electrolytically precipitating or with other metals precipitating the metal on a conducting-plate, then Washing the same and fixing it on the plate by rolling, in the manner described.
In Witness whereof I have hereunto set my hand in presence of tWo Witnesses.
FRIEDRICH MARX. Witnesses:
EUSTACE HOPKINS, PAUL AULIoH.
Publications (1)
Publication Number | Publication Date |
---|---|
US425335A true US425335A (en) | 1890-04-08 |
Family
ID=2494249
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US425335D Expired - Lifetime US425335A (en) | Friedrich marx |
Country Status (1)
Country | Link |
---|---|
US (1) | US425335A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2610219A (en) * | 1950-04-04 | 1952-09-09 | Yardney International Corp | Rechargeable battery |
-
0
- US US425335D patent/US425335A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2610219A (en) * | 1950-04-04 | 1952-09-09 | Yardney International Corp | Rechargeable battery |
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