US1358626A - Depolarizing agent for dry batteries and process of making same - Google Patents
Depolarizing agent for dry batteries and process of making same Download PDFInfo
- Publication number
- US1358626A US1358626A US199424A US19942417A US1358626A US 1358626 A US1358626 A US 1358626A US 199424 A US199424 A US 199424A US 19942417 A US19942417 A US 19942417A US 1358626 A US1358626 A US 1358626A
- Authority
- US
- United States
- Prior art keywords
- manganese
- dioxid
- dry batteries
- making same
- making
- 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
- 238000000034 method Methods 0.000 title description 14
- 230000002999 depolarising effect Effects 0.000 title description 7
- GOPYZMJAIPBUGX-UHFFFAOYSA-N [O-2].[O-2].[Mn+4] Chemical compound [O-2].[O-2].[Mn+4] GOPYZMJAIPBUGX-UHFFFAOYSA-N 0.000 description 20
- 239000011572 manganese Substances 0.000 description 14
- 229910052748 manganese Inorganic materials 0.000 description 13
- 239000000047 product Substances 0.000 description 12
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 11
- 229910002651 NO3 Inorganic materials 0.000 description 11
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 11
- 235000002908 manganese Nutrition 0.000 description 11
- 239000005708 Sodium hypochlorite Substances 0.000 description 10
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 10
- 239000002244 precipitate Substances 0.000 description 9
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 5
- 229910017604 nitric acid Inorganic materials 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229940099408 Oxidizing agent Drugs 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000036571 hydration Effects 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(2+);dinitrate Chemical compound [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 101100001675 Emericella variicolor andJ gene Proteins 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002697 manganese compounds Chemical class 0.000 description 1
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Inorganic materials O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G45/00—Compounds of manganese
- C01G45/02—Oxides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/80—Compositional purity
Definitions
- This invention relates to a process of making manganese dioxid substantially or entirely free from manganites thereby yielding a product suitable as a de olarizing agent for dry batteries of the eclanch type and relates particularly to a finely-divided black precipitate of manganese dioxid containing relatively small amounts of water of hydration or being entirely free therefrom which may be prepared in the manner set forth below.
- This product is preferably secured by simultaneously reacting on a manganous compound with two or more oxidizing agents, for example, nitric acid and hypochlorous acid or sodium hypochlorite and nitric acid.
- oxidizing agents for example, nitric acid and hypochlorous acid or sodium hypochlorite and nitric acid.
- a mixture especially suited for such reaction is manganous nitrate and sodium hypochlorite which when heated to boiling in fairly concentrated solution yield a black precipitate of manganese dioxld substantially free from manganites and which contains about 95% MnO Manganous nitrate when heated alone produces manganese dioxid but not i n so pure a state as that obtained by the ]O1nt action of hypochlorite. While it is not necessary to have one oxidizing agent com- Specification of Letters Patent.
- manganous base itis preferable and manganous nitrate, chlorate and the like is suitable for this purpose.
- manganese nitrate hydrated was melted in its own water of hydration until it began to decompose forming manganese dioxid or a body containing the latter. A concentrated solution of sodium hypochlorite was added slowly, the rate of addition being such as to keep the volume of the solution constant. The reaction was very violent. The manganese dioxid produced was filtered off and was found to be of high purity.
- the product obtained by such powerful oxidation or efi'ect of this duplex oxidizing agent may, if desired, be treated in some cases by extraction with an acid such as dilute nitric acid to remove any residue of acid soluble material, iron, etc., or successive extraction with nitric and then with sulfuric acid may be employed.
- the product is then well washed and dried. The drying C. or higher in order to eliminate as far as possible any free or combined water.
- the invention involved herein embraces a new product, namely a depolarizing agent consisting of or comprising a higher oxld of manganese compound or material preferably in the form of a black precipitate containing at least 95% MnO in a slightly hydrated condition and of medium conductivity for the electric current and in the preferred form manifesting a slight lag or hysteresis of conductivity which is d1fierent from ordinary mineral manganese dioxid (pyrolusite) or artificial normally-hydrated artificial manganese dioxid which conduct the electric current Without noticeable lag.
- a depolarizing agent consisting of or comprising a higher oxld of manganese compound or material preferably in the form of a black precipitate containing at least 95% MnO in a slightly hydrated condition and of medium conductivity for the electric current and in the preferred form manifesting a slight lag or hysteresis of conductivity which is d1fierent from ordinary mineral manganese dioxid (pyrolusite
- a finely-divided black precipitate containing at least- 95% Mn 2 and possessing a substantially greater conductivity lag than pure hydrated magganese dioxid depolarizers heretofore use 11.
- a depolarizing agent comprising precipitated slightly hydrated manganese material containing over 95% MnO and possessing a conductivity lag at least three times as great as the ordinary pure hydrated manganese depolarizer.
- a depolarizing agent comprising precipitated slightly hydrated manganese material containing over 95% MnO and possessing a conductivity lag of a greater order of magnitude than ordinary pure hydrated MnO depolarizer.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Description
UNITED STATES PATENT OFFICE.
CARLETON ELLIS, OF MONTCLAIR, NEW JERSEY, ASSIGNOR, BY MESN'E ASSIGNMENTS, T0 NATIONAL CARBON COMPANY, INC., 015 NEW YORK, N. Y., A CORPORATION OF NEW YORK.
DEPOLARIZING AGENT FOR DRY BATTERIES AND PROCES-S OF MAKING SAME.
No Drawing.
To all whom it may concern: 7
Be it known that I, CARLE'roN ELLIs, a citizen of the United States, and a'resident of Montclairfin the county of Essex and State of New Jersey, have invented certain new and useful Improvements in Depolarizing Agents for Dry Batteries and Processes of Making Same, of which the following is a specification.
This invention relates to a process of making manganese dioxid substantially or entirely free from manganites thereby yielding a product suitable as a de olarizing agent for dry batteries of the eclanch type and relates particularly to a finely-divided black precipitate of manganese dioxid containing relatively small amounts of water of hydration or being entirely free therefrom which may be prepared in the manner set forth below.
In the oxidation of many of the compounds of manganese in the manganous condition only a partial conversion of manganese dioxid is secured ranging in some cases from 40 or 50% to 70 or 80% under other conditions. Often a portion of the man ganese dioxid unites with some of the manganous material to form a manganous manganite which is quite resistant to further oxldation so that if the conditions are such that the product is formed even very drastic oxidation treatment does not yield a productdof a high percentage of manganese di 0x1 According to the present invention a product containing at least 95% of manganese dioxid and normally 98 to 99% is obtained. This product is preferably secured by simultaneously reacting on a manganous compound with two or more oxidizing agents, for example, nitric acid and hypochlorous acid or sodium hypochlorite and nitric acid. A mixture especially suited for such reaction is manganous nitrate and sodium hypochlorite which when heated to boiling in fairly concentrated solution yield a black precipitate of manganese dioxld substantially free from manganites and which contains about 95% MnO Manganous nitrate when heated alone produces manganese dioxid but not i n so pure a state as that obtained by the ]O1nt action of hypochlorite. While it is not necessary to have one oxidizing agent com- Specification of Letters Patent.
Application filed October 31, 1917. Serial No. 199,424.
bined with the manganous base itis preferable and manganous nitrate, chlorate and the like is suitable for this purpose.
An illustration of one method of carrying out the invention is as follows:
5 parts by weight of manganous nitrate (6H O) was dissolved in 20 parts of water and 10 parts of a 30% solution of sodium hypochlorite was added. This mixture was heated to boiling and an abundant precipitate of black manganese dioxid containing over 95% MnO (a small amount of water of hydration was present) was obtained. In another case the hypochlorite was added in successive portions, and the manganese dioxid formed was filtered off after each addition. The product contained approximately a like content of Mn(),. A portion of the dioxid obtained by this process was boiled for a few minutes with a 10% solution of sulfuric acid. Practically no manganese was dissolved. The product exhibited medium conducting properties.
In another case manganese nitrate (hydrated) was melted in its own water of hydration until it began to decompose forming manganese dioxid or a body containing the latter. A concentrated solution of sodium hypochlorite was added slowly, the rate of addition being such as to keep the volume of the solution constant. The reaction was very violent. The manganese dioxid produced was filtered off and was found to be of high purity.
Some of the material obtained in this manner exhibits a peculiar lag or hysteresis of electrical conductivity.
If a column of manganese dioxid prepared according to the present invention is connected in series with a lamp and a source of potential, a considerable time will elapse before the current through the circuit rises to its full value, as indicated by the fact that the lamp will light (a sufficient potential being employed) but only after a lapse of time. If commercial hydrated manganese dioxid of approximately the same degree of purity is tested in a similar way, it ma also indicate a slight lag in conductivity, but in the case of the material heretofore known, the lag, measured in seconds, will be less than one-third of that exhibited by my novel product, according to measurements which have been made. In some may take place at 100 described product, but in general, it is about one-twelfth as great.
The product obtained by such powerful oxidation or efi'ect of this duplex oxidizing agent may, if desired, be treated in some cases by extraction with an acid such as dilute nitric acid to remove any residue of acid soluble material, iron, etc., or successive extraction with nitric and then with sulfuric acid may be employed. The product is then well washed and dried. The drying C. or higher in order to eliminate as far as possible any free or combined water.
The invention involved herein embraces a new product, namely a depolarizing agent consisting of or comprising a higher oxld of manganese compound or material preferably in the form of a black precipitate containing at least 95% MnO in a slightly hydrated condition and of medium conductivity for the electric current and in the preferred form manifesting a slight lag or hysteresis of conductivity which is d1fierent from ordinary mineral manganese dioxid (pyrolusite) or artificial normally-hydrated artificial manganese dioxid which conduct the electric current Without noticeable lag.
What I claim is:
1. The process of making manganese dioxid substantially free from manganites which comprises heating manganous nitrate in the presence of sodium hypochlorite.
2. The process of making manganese dioxid substantially free from manganites which comprises heating manganous nitrate in the presence of a hypochlorite.
3. The process of making manganese dioxid which comprises heating a compound of manganese and nitric acid in the presence of a hypochlorite.
4. The process of making manganese dioxid substantially free from manganites which comprises reacting on manganous nitrate with sodium hypochlorite.
5. The process of making manganese dias h the herein-- of manganous nitrate with an added oxidiz ing agent. 7
6. he process of making man anese dioxid containing over 95% Mn which comprises boiling a solution of manganous nitrate and sodium hypochlorite, in collecting the precipitate, washing and extracting the residue with dilute nitric acid and finally washing the acid. extracted residue with dilute sulfuric acid.
7 The process of making manganese dioxid which comprises boiling a solution of manganous nitrate and sodium hypochlorite, in collecting the precipitate, washing andJ 1 extracting the residue with dilute nitric aci 8. The process of making manganese dioxid which comprises boiling a concentrated solution of manganous nitrate and sodium hypochlorite, in collecting the precipitate and washing the latter.
9. The process of making manganese dioxid which comprises adding to a boiling solution of manganese nitrate successive portions of sodium hypochlorite, and collecting and washing the precipitate.
10. As a new product higher oxid of manganese depolarizing material, a finely-divided black precipitate containing at least- 95% Mn 2 and possessing a substantially greater conductivity lag than pure hydrated magganese dioxid depolarizers heretofore use 11. A depolarizing agent comprising precipitated slightly hydrated manganese material containing over 95% MnO and possessing a conductivity lag at least three times as great as the ordinary pure hydrated manganese depolarizer.
12. A depolarizing agent comprising precipitated slightly hydrated manganese material containing over 95% MnO and possessing a conductivity lag of a greater order of magnitude than ordinary pure hydrated MnO depolarizer.
GARLETON ELLIS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US199424A US1358626A (en) | 1917-10-31 | 1917-10-31 | Depolarizing agent for dry batteries and process of making same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US199424A US1358626A (en) | 1917-10-31 | 1917-10-31 | Depolarizing agent for dry batteries and process of making same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1358626A true US1358626A (en) | 1920-11-09 |
Family
ID=22737439
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US199424A Expired - Lifetime US1358626A (en) | 1917-10-31 | 1917-10-31 | Depolarizing agent for dry batteries and process of making same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1358626A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3640683A (en) * | 1969-01-28 | 1972-02-08 | Mitsui Mining & Smelting Co | Method of preparing manganese dioxide for dry cell |
| US4006217A (en) * | 1974-04-23 | 1977-02-01 | Rheinisch-Westfallisches Elektrizitatswerk Aktiengesellschaft | Process for making manganese dioxide |
-
1917
- 1917-10-31 US US199424A patent/US1358626A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3640683A (en) * | 1969-01-28 | 1972-02-08 | Mitsui Mining & Smelting Co | Method of preparing manganese dioxide for dry cell |
| US4006217A (en) * | 1974-04-23 | 1977-02-01 | Rheinisch-Westfallisches Elektrizitatswerk Aktiengesellschaft | Process for making manganese dioxide |
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