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US1361499A - Manufacture of dry cells - Google Patents

Manufacture of dry cells Download PDF

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Publication number
US1361499A
US1361499A US355244A US35524420A US1361499A US 1361499 A US1361499 A US 1361499A US 355244 A US355244 A US 355244A US 35524420 A US35524420 A US 35524420A US 1361499 A US1361499 A US 1361499A
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United States
Prior art keywords
core
electrolyte
mixture
zinc
solution
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Expired - Lifetime
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US355244A
Inventor
Otto E Ruhoff
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French Battery & Carbon Co
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French Battery & Carbon Co
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Priority to US355244A priority Critical patent/US1361499A/en
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Publication of US1361499A publication Critical patent/US1361499A/en
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/04Cells with aqueous electrolyte
    • H01M6/06Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid
    • H01M6/08Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with cup-shaped electrodes
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/49108Electric battery cell making

Definitions

  • IwIIoFr or MADISON, wIscoNsIN, AssreNoR 'ro FRENCH BATTERY & CARBON 00., or MADISON, wIsooNsIN, A coRroRATIoN or wIscoNsIN.
  • the presentinvention relates to a method and the primary objectis to provide an improved and thoroughly practicable method of manufacturing dry cells without the use of a cheesecloth covering for the depolarizing core, or without the use of a bibulous sheet of material between the depolarizing core and the surrounding wall of the zinc container.
  • Figure 1 represents a perspective view of a depolarizing core having attached to vits lower end, as by means of any suitable adhesive, a spacing member;
  • Fig. 2 a sectional view of the container and a broken view of the lower portion of the core, illustrating the manner in which the core is to be introduced into the container;
  • Fig. 3 a sectional view illustrating the core and electrolyte in the can and showing the manner in which the core is held in a centered position while the electrolyte is being gelatinized.
  • the preferred method of manufacture is to compound an electrolyte mixture comprising a solution of ammonium 'chlorid, zinc chlorid, and a starchy material, which is adapted to gelatinize by the action of one or both of the chlorids; pour a suitable quanthis electrolyte mixture into the zinc can, as indicated in Fig.
  • the spacing member D serves as a centering device, and the core causes displacement of the electrolyte, causing it to fill the annular space between the core and the surrounding wall of the can; then apply the temporarily used centering device E tohold the electrode and core properly centered at the upper end; and then immediately introduce the can and its contents into hot water to cause the starch to become quickly gelatinized, WhlCll results in the electrolyte becoming setg or assuming a thick, firm, jelly-like consistency.
  • the gelatinization may be efiected very quickly.
  • the gelatinizing operatlon may. be performed in from two to five seconds.
  • the depolarizing mixture of the core usually comprises manganese dioxid, earbonaceous material, sal ammoniac (ammonium chlorld) and suflicient water for compacting purposes. If desired, some binder ingredient of a sticky or cementitious character may be introduced into the material before the compacting operation. A boiled mixture of flour and water will serve, or the solid materials of the core may be moistened before the compacting operation with a syrupy fluid comprising a solution of zinc chlorid and water and a small percentage of starch, gelatinized by said solution.
  • the core of the depolarizing mixture is comparatively fragile and lacking in tenacity, and comparatively easily permeable by a watery solution, or by a'thinly 'fluid mixture, such as ordina electrolyte,
  • a suitable electrolyte may be prepared as follows (a) dissolve 1034 grams of sal ammoniac in 1990 c. c. of 45 Baum zinc chlorid solution; (1)) dissolve 882 grams of sal ammoniac in 1307 c. c. of water; (0) make a thin paste by thoroughly mixing 50 grams of cornstarch and 200 c. c. of water; (a?) then add this paste to the zinc chlorid and sal ammoniac solution (of step a) in a container suitable for thorough agitation and stir until all the starch paste is set or gelatinized; (6) then add the sal ammoniac solution (of step b) and agitate until the mixture is uniform and of a thin syrupy consistency.
  • the mixture thus formed has the property of being sufficiently pasty to act on the surface of the core to keep out the water which otherwise might dislntegrate the core in case the cheesecloth cover were omitted, but, nevertheless, is sufliciently fluid to facilitate the manu facture of the cell.
  • the use of this initially gelatinous material in the electrolyte tends to prevent any disinte ration during the slight interval which mtervenes before the heating opera tion is performed.
  • the electrolyte may be prepared by mixing the sal ammoniac, and zinc chlorid solution, and Water, in the proportions indicated above, and thoroughly mixing with the solution aquantity of raw starch, sufiicient to give the proportions in the complete electrolyte mixture noted above.
  • the electrolyte and core can then be introduced into the can, and the can instantly placed in hot water to effect the gelatinization of the electrolyte.
  • a suitable washer may be introduced into the upper portion of the can and the upper portion of the can may then be filled with molten pitch, which upon setting effectively seals the cell. It is usual, of course, to leave an air space below the pitch seal to compensate for the expansion of the electrolyte or the generation of gas.
  • the invention renders thoroughly prac-' ticable the use of a naked, or unwrapped core.
  • This core can be introduced into the can in the manner set forth without danger of disintegration and without danger of short-circuiting the cell.
  • the cost of manufacturing cells'can be reduced, which is a matter of prime importance in an article WlllCll 1s used in very large numbers.
  • a further advantage of this type of construction is that air is not trapped between the core and can and the electrolyte can establish contact at all points with the periph eral surfaces of coreand can. Also, the internal resistance of the cell is somewhat lessened.
  • the invention renders thoroughly practicable the useof a naked, or unwrapped core.
  • electrolyte composed of a solution of sal ammoniac and zinc chlorid, mixed with raw starch alone
  • this method is preferred. If, however, the steps of manufacture are so carried out as to cause any substantial interval of time to elapse before the cells are introduced into hot Water, then it is preferred to employ the electrolyte mixture containing a small percentage of initially gelatinized starch. In such case, it is desirable to keep on hand a complete stock mixture of the character described above containing a small percentage of gelatinized starch, and add thereto a larger quantity of raw starch just before introducing the electrolyte mixture into the can.
  • the process of manufacturing a dry cell which comprises: compounding an electrolyte mixture comprising a solution of ammonium chlorid and zinc chlorid and material adapted to gelatinize; introducing said mixture and a naked core of depolarizing mixture into a zinc can; and immediately subjecting the can and its contents to the action of heat to effect quick gelatinization of the electrolyte.
  • the process of manufacturing a dry Y cell which comprises: compounding an electrolyte mixture comprising a solution of ammonium chlorid and zinc chlorid and ungelatinized starch; introducing said mixture and a naked core of depolarizing mixture into a zinc can; and immediately subjecting the can and its contents to the action of heat to effect quick gelatinization of. the starch.

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  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Primary Cells (AREA)
  • Cell Separators (AREA)

Description

0. E. RUHOFF.
MANUFACTURE OF DRY CELLS.
APPLICATION FILED JAN-30, I920.
1,361,499. I Patented Dec. 7,1920.
-jfmsvzhr of manufacturing dry cells;
tity of uNirEe sTA'rEs am orricrz.
or'ro E. IwIIoFr, or MADISON, wIscoNsIN, AssreNoR 'ro FRENCH BATTERY & CARBON 00., or MADISON, wIsooNsIN, A coRroRATIoN or wIscoNsIN.
MANUFACTURE OF DRY CELLS.
Specification of Letters Patent.
Patented Dec. 7, 1920.
Application filed January 30, 1920. Serial No. 355,244.
Toall whom it may concern Be it known that I, O'r'ro E. RUHorr, a citizen of the United States, residin at Madison, in the county of Dane and btate of Wisconsin, have invented a new and useful Improvement in the Manufacture of Dry Cells, of which the following is a specification.
The presentinvention relates to a method and the primary objectis to provide an improved and thoroughly practicable method of manufacturing dry cells without the use of a cheesecloth covering for the depolarizing core, or without the use of a bibulous sheet of material between the depolarizing core and the surrounding wall of the zinc container.
The improved process is illustrated in the accompanying drawing, in which Figure 1 represents a perspective view of a depolarizing core having attached to vits lower end, as by means of any suitable adhesive, a spacing member; Fig. 2, a sectional view of the container and a broken view of the lower portion of the core, illustrating the manner in which the core is to be introduced into the container; and Fig. 3, a sectional view illustrating the core and electrolyte in the can and showing the manner in which the core is held in a centered position while the electrolyte is being gelatinized.
In the illustration given, A rep-resents the usual zinccan of a dry cell; B, a suitable electrolyte, which is adapted to gelatinize, or assume a thick, pasty consistency; C, a core of depolarizing material having embedded therein a carbon electrode C whose upper end projects above the upper end of the core; D, a separator member in the form of a disk of rather stiff flexible paraifined paper, secured to the lower end of the core, as by means of a suitable adhesive; and E, a temporary centering device in the upper portion of the core.
The preferred method of manufacture is to compound an electrolyte mixture comprising a solution of ammonium 'chlorid, zinc chlorid, and a starchy material, which is adapted to gelatinize by the action of one or both of the chlorids; pour a suitable quanthis electrolyte mixture into the zinc can, as indicated in Fig. 2; then insert the core into the can, during which operation the spacing member D serves as a centering device, and the core causes displacement of the electrolyte, causing it to fill the annular space between the core and the surrounding wall of the can; then apply the temporarily used centering device E tohold the electrode and core properly centered at the upper end; and then immediately introduce the can and its contents into hot water to cause the starch to become quickly gelatinized, WhlCll results in the electrolyte becoming setg or assuming a thick, firm, jelly-like consistency. The gelatinization may be efiected very quickly. Thus, by introducing the can and its contents into water having a temperature of about 80 0., the gelatinizing operatlon may. be performed in from two to five seconds. This heat treatment should follow very promptly the introduction of the electrolyte and core into the can. If the core be allowed to stand in the electrolyte for any considerable time, before effecting gelatinization, the electrolyte, because of its watery character, tends to rapidly disintegrate the core, and may destroy the usefulness of the cell.
The depolarizing mixture of the core usually comprises manganese dioxid, earbonaceous material, sal ammoniac (ammonium chlorld) and suflicient water for compacting purposes. If desired, some binder ingredient of a sticky or cementitious character may be introduced into the material before the compacting operation. A boiled mixture of flour and water will serve, or the solid materials of the core may be moistened before the compacting operation with a syrupy fluid comprising a solution of zinc chlorid and water and a small percentage of starch, gelatinized by said solution. In any event, however, the core of the depolarizing mixture is comparatively fragile and lacking in tenacity, and comparatively easily permeable by a watery solution, or by a'thinly 'fluid mixture, such as ordina electrolyte,
before the starchy content'ha been gelatinized. Hence, it is desirable, immediately after the core has been introduced into the electrolyte, to subject the can and its contents to heat action to effect gelatinization before any appreciable disintegration of the core can result.
A suitable electrolyte may be prepared as follows (a) dissolve 1034 grams of sal ammoniac in 1990 c. c. of 45 Baum zinc chlorid solution; (1)) dissolve 882 grams of sal ammoniac in 1307 c. c. of water; (0) make a thin paste by thoroughly mixing 50 grams of cornstarch and 200 c. c. of water; (a?) then add this paste to the zinc chlorid and sal ammoniac solution (of step a) in a container suitable for thorough agitation and stir until all the starch paste is set or gelatinized; (6) then add the sal ammoniac solution (of step b) and agitate until the mixture is uniform and of a thin syrupy consistency. The mixture thus formed has the property of being sufficiently pasty to act on the surface of the core to keep out the water which otherwise might dislntegrate the core in case the cheesecloth cover were omitted, but, nevertheless, is sufliciently fluid to facilitate the manu facture of the cell.
To the thin syrupy mixture, thus obtained, is 7 added ordinary ungelatinized starch, flour, or other cereal in the proportion of 160 c. c. of the'above mixture and grams of corn starch or other cereal. The complete electrolyte mixture, still liquid, is now poured into the space between the core and zinc can, and the gelatinization is effected by immersing the can in hot water. If desired, a sufiicient quantity of electrolyte can be poured into the can, and the core can be inserted in the manner illustrated and described.
The use of this initially gelatinous material in the electrolyte tends to prevent any disinte ration during the slight interval which mtervenes before the heating opera tion is performed. By immediately introducing the cell into hot water, however, the use of the initially gelatinized material may be rendered unnecessary. In such case, the electrolyte may be prepared by mixing the sal ammoniac, and zinc chlorid solution, and Water, in the proportions indicated above, and thoroughly mixing with the solution aquantity of raw starch, sufiicient to give the proportions in the complete electrolyte mixture noted above. The electrolyte and core can then be introduced into the can, and the can instantly placed in hot water to effect the gelatinization of the electrolyte.
In any case, after the electrolyte has become set, a suitable washer may be introduced into the upper portion of the can and the upper portion of the can may then be filled with molten pitch, which upon setting effectively seals the cell. It is usual, of course, to leave an air space below the pitch seal to compensate for the expansion of the electrolyte or the generation of gas.
The invention renders thoroughly prac-' ticable the use of a naked, or unwrapped core. This core can be introduced into the can in the manner set forth without danger of disintegration and without danger of short-circuiting the cell. Thus, the cost of manufacturing cells'can be reduced, which is a matter of prime importance in an article WlllCll 1s used in very large numbers. A further advantage of this type of construction is that air is not trapped between the core and can and the electrolyte can establish contact at all points with the periph eral surfaces of coreand can. Also, the internal resistance of the cell is somewhat lessened.
The invention renders thoroughly practicable the useof a naked, or unwrapped core.
Inasmuch as it is feasible, by operating quickly, to use electrolyte composed of a solution of sal ammoniac and zinc chlorid, mixed with raw starch alone, this method is preferred. If, however, the steps of manufacture are so carried out as to cause any substantial interval of time to elapse before the cells are introduced into hot Water, then it is preferred to employ the electrolyte mixture containing a small percentage of initially gelatinized starch. In such case, it is desirable to keep on hand a complete stock mixture of the character described above containing a small percentage of gelatinized starch, and add thereto a larger quantity of raw starch just before introducing the electrolyte mixture into the can.
The foregoing detailed description has been given for clearness of understanding only, and no unnecessary limitation should be understood therefrom, but the appended claims should be construed as broadly as permissible, in view of the prior art.
What I regard as new and desire to secure .by Letters Patent is:.
1. The process of manufacturing a dry cell, which comprises: compounding an electrolyte mixture comprising a solution of ammonium chlorid and zinc chlorid and material adapted to gelatinize; introducing said mixture and a naked core of depolarizing mixture into a zinc can; and immediately subjecting the can and its contents to the action of heat to effect quick gelatinization of the electrolyte.
2. The process of manufacturing a dry Y cell, which comprises: compounding an electrolyte mixture comprising a solution of ammonium chlorid and zinc chlorid and ungelatinized starch; introducing said mixture and a naked core of depolarizing mixture into a zinc can; and immediately subjecting the can and its contents to the action of heat to effect quick gelatinization of. the starch.
3. The process of manufacturing a dry 'cell, which comprises: compounding an electrolyte mixture comprising a solution of ammonium chlorid and zinc chlorid and material adapted to gelatinize; pouring a quantlty of said mlxture into a ZlIlC can; msertmg a naked core of depolarizing mixture equippedwith a spacing member which serves as a centering devlce, said core ef-.
fecting displacement of ing the inserting operation; ately subjecting the can and the actior of heat to quickly 5 trolyte.
4. The process of manufa the electrolyte durand immediits contents to set the eleccturing a dry cell which comprises: compounding an electrolyte mixture comprising a solution of ammonium chlorid and Zinc chlorid and raw 10 starch; pouring a quantity 0 i said mixture into a zinc can; inserting a naked core of depolarizing face equipped with a spacing member which serves as a centering device, said core effecting displacement of the electrolyte during the inserting operation; and placing the cell in a hot liquid to quickly set the electrolyte. I
OTTO E. nUHorF.
mixture having its bottom sur--
US355244A 1920-01-30 1920-01-30 Manufacture of dry cells Expired - Lifetime US1361499A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2962844A (en) * 1955-10-14 1960-12-06 Orlando Matthew Machine for making dry cells

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2962844A (en) * 1955-10-14 1960-12-06 Orlando Matthew Machine for making dry cells

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