CA1061856A - Self-pumping electrochemical cell - Google Patents

Self-pumping electrochemical cell

Info

Publication number
CA1061856A
CA1061856A CA232,686A CA232686A CA1061856A CA 1061856 A CA1061856 A CA 1061856A CA 232686 A CA232686 A CA 232686A CA 1061856 A CA1061856 A CA 1061856A
Authority
CA
Canada
Prior art keywords
cell
anode
electrolyte
cathode
interior
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
Application number
CA232,686A
Other languages
French (fr)
Inventor
Leroy S. Rowley
Harry J. Halberstadt
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lockheed Martin Corp
Original Assignee
Lockheed Missiles and Space Co Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lockheed Missiles and Space Co Inc filed Critical Lockheed Missiles and Space Co Inc
Application granted granted Critical
Publication of CA1061856A publication Critical patent/CA1061856A/en
Expired legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/26Cells without oxidising active material, e.g. Volta cells
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/70Arrangements for stirring or circulating the electrolyte
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing 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)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
  • Primary Cells (AREA)

Abstract

ABSTRACT

In a reactive metal-water electrochemical cell, a configuration utilizing waste heat and evolved hydrogen gas for pumping electrolyte through the cell. More particularly, the cell is in a vertical, hollow tubular con-figuration with the reactive anode being bonded to the interior surface of the tube casing and a coiled metal screen cathode being positioned within the tubular cell and contacting the anode over essentially its full working sur-face. As the anode is consumed in operation, by reaction with an aqueous electrolyte filling the interior cavity of the tubular configuration, the coil configuration of the cathode forces it to expand and maintain contact with the anode. During operation, evolved waste heat and gas cause a flow of electrolyte through the interior of the cell.

Description

This application describes and claims certain improvements in the basic electrochemical cell disclosed in United States patent 3,791,871.
The basic mechanism of the cell is described in United States pat-ent 3,791,871. Briefly, the cell utilizes a reactive metal anode highly reactive with an aqueous electrolyte and spaced from the cathode by an elec~, trically insulating film which forms naturally on the anode in the presence of water. This thin film permits the cathode to be placed in direct contact with the anode. The resulting reduction in the anode-cathode spacing to a thickness no greater than the thickness of this film greatly reduces the I2R
-` 10 losses which would otherwise be present and results in increased power output and energy density. The anode and cathode operate in an aqueous electrolyte which supports the beneficial electrochemical reaction. The cathode is beneficially formed of an open-mesh metallic screen contoured to contact the anode over substantially the entire operating surface.
~uring operation of the cell, molarity of the electrolyte increases with a resulting decrease in power output. Further, excess heat must be re-moved from the electrolyte which would otherwise result in a loss of effici-ency. Likewise, depolarization of the cell must be accomplished by removal of hydrogen gas evolved at the cathode. Accordingly, the electrolyte is ` 20 normally pumped through the cell in order to remove heat, bring in additional ;; oxidant to maintain desired molarity and remove hydrogen. The use of mech-anical pumps and heat exchangers for this purpose are cumbersome, consume power and generate noise, all of which are undesirable.
This invention relates to a self-pumping reactive metal anode-aqueous electrolyte electrochemical cell consisting essentially of a vertical hollow tubular casing, a reactive anode bonded to the interior surface of said casing, said anode naturally forming on its surface a protective insul-ating film in the presence of water, an expandable coiled metal open-mesh - screen cathode positioned within the interior of said tubular casing and con-tacting said insulating film over substantially all of the anode surface .' ,.. . :
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facing said cathode, said cathode pressing continuously against said insulating film during operation of said cell, an aqueous electrolyte filling the interior cavity of said hollow tubular casing and flowing from the bottom to the top of said cell, and a reservoir containing aqueous electrolyte in fluid communication with the top and bottom of said cell, whereby electrolyte is drawn up through said cell by evolved heat and gas generated during operation of said cell and electrolyte is drawn down through said reservoir as it cools.
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Briefly, in accordance with the invention, there is described a configuration which dispenses with the necessity of mechanical pumps and heat exchangers and, by use of the products of the electrochemical reaction, is self-pumping, the pumping force being supplied by the waste heat and hydrogen gas evolved. The configuration has the further advantage of reduc-ing non-working anode edge surfaces which would normally be exposed to the electrolyte and therefore subject to parasitic erosion.
More particularly, in accordance with the invention, a reactive anode is bonded to the interior surface of a tubular casing and a coiled metal screen cathode is positioned within the casing. The coiled screen presses continuously against the working surface of the anode during the lifetime of the battery. The circular construction of the anode does not provide ~ny non-working exposed edges other than the small top and bottom seams at the ends of the tube and parasitic erosion is accordingly minimized.
- During operation, reaction of the lithium with the electrolyte in the in-terior cavity of the casing causes the electrolyte to be heated thereby establishing a thermal gradient in the cell. This gradient and the buoyancy : .
of the hydrogen gas evolved at the cathode creates a flow of electrolyte through the cell, with hot electrolyte containing hydrogen gas exiting from - 20 the top of the cell and fresh oxidant being drawn into the bottom of the cell.
The various features and advantages of the invention will become apparent upon consideration of the following description taken in conjunction with the accompanying drawing of the preferred embodiment of the invention.
The views of the drawing are as follows:
~ FIGURE 1 is a top view of two self-pumping cells of the invention .- operating from a common reservoir; and ~.
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FIGURE 2 is a edge cross-sectional view of the cells of Figure l.
With reference to Figures 1 and 2, where like reference characters designate corresponding parts throughout the several views, there is depicted two cells of the invention 1 and 2 operating, in this.embodiment, from a com-mon reservoir 3. Reactive metal anodes 4 are bonded, for example by metal-urgical means, to the inside walls of the tubular metal casings 5. me in-sulating film 6 which forms naturally on anodes 4 electrically separates an-odes 4 from expanding coiled metal screen cathodes 7. As the anode 4 is con-sumed in operation, the cathode 7 expands to maintain contact with the anode.
A cathode current collector 8 is bonded to each screen cathode 7 and an an-ode connector 9 is bonded to the exterior of each cell casing 5.
In the embodiment shown in the drawing, two cells l and 2 are con-nected to a central reservoir 3 by means of pipes 10 and 11. me upper pipes 10 are for egress of the circulating electrolyte 12 and the lower pipes ll are for ingress of the electrolyte into the cells. To enhance rejection of heat to the environment the depicted cells and central reservoir may be im_ mersed in a liquid bath such as water. If the liquid bath is an electrically conducting fluid, the exterior surfaces of metal casings ~5) are electrically insulated, for example, with an insulating epoxy paint, not shown. Natur- --ally, there may be only one or more than two cells connected to a central reservoir instead of the two cells depicted in the drawing.
; As the cells operate, the electrolyte 12 circulates down through the reservoir 3 as it cools and evolves the entrained hydrogen and enters the cells 1 and 2 by way of pipes 11. Evolved hydrogen is vented through relief valve 13. Oxidant, norm~lly water, is admitted through inlet pipe 14 as ~e-quired to keep the cells operating at the desired power level.
; As discussed in United States Patent 3,791,871, molarity of the ,::. .
electrolyte is varied to control power output of the ceIls. Whereas conven-- tional batteries decline in both voltage and power during discharge reaching a point of unacceptable low voltage before the active materials are consumedS

'~: ' ' ti voltage and power in the cells of the invention are maintained at the desired level throughout the life of the anode. The voltage and power output per unit area of cel~s of the invention are primarily dependent on electrolyte concen-tration and temperature. The temperature is maintained relatively constant by the configuration of the cells of the invention. Accordingly, control of voltage and power is accomplished by varying the molarity of the electrolyte~
~uring operation, the cells of the invention produce a reactive metal hydrox-ide at the anode which tends to reduce power output as the concentration ex-ceeds in optimum molarity which can be readily calibrated. Accordingly, an oxidant, typically water, is added to the electrolyte to control molarity, that is, reduce the hydroxide concentration~ The control function used to control power output is total cell voltage. Variations of voltage above or below the desired level is sensed by an electronic sensor which actuates a solenoid value which in turn controls the rate of water addition through pipe :. ~
14 to the electrolyte. Excess electrolyte generated by such oxidant additions is vented through valve 13.
Anode 4 is formed of a reactive metal such as sodium or lithium which is highly reacting with and in the presence of water naturally forms on its surface a protective insulating film. Alloys and compounds of such ;
alkali metals and other reac~ive metals should be equally feasible for use as the anode provided they are substantially as reactive with water as are , sodium and lithium and furtherprovided, in common with sodium and lithium, they naturally form a continuous insulating film in the presence of water.
The open-mesh screen cathode is of any suitable electrically conductive material which is non-reactive with water and will permit electrochemical reduction of water during operation of the cell. Illustratively, iron and nickel are preferred materials with black platinum and black nickel provid-ing increased efficiency at the expense of high cost and reduced durability.
The minimum size of the screen is governed by the need to get ., .
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electrolyte to the anode face plus the need to remove the products of reaction away from the face. The maxLmum screen si~e is governed by the desire to keep all parts of the anode face as near as possible to the cathode. Illus-tratively, for an anode surface measuring 5 inches by 11 inches, a metal screen- with 0,003 inch metal and 0 1 inch by 0.5 inch openings has produced excellent results.
During operation, the cells of the invention produce a metal hydr_ oxide, the particular metal being dependent on the composition of the anode.
Accordingly, for ease of operation, the aqueous electrolyte is preferably the same as that produced by the reactive metal-water reaction. However, any one of a number of other aqueous solutions sho~ld be equally feasible as a s~art-ing electrolyte provided such electrolytes have the requisite film forming charac~eristics, When dry storage is desired the reservoir 3 may be filled with appropriate dry electrolytes such as lithium hydroxide monohydrate and the cell activated by the introduction of water into the reservoir~
While a central reservoir is not required for single or multiple cell operation, it is considered desirable for multiple cell operation in that the reservoir contributes to maintaining electrical balance between multiple .:. .
-~ cells by providing all cells with electrolyte of equal molarity and temper-ature.
Illustratively, four tubular cells, 6 inches long and 1 inch in diameter, containing 1/8-inch of lithium bonded to the ~nner walls of each ` tube for a length of 52linches, were operated connected to a central reservoir containing 1,0 molar lithium hydroxide solution in LiC1 for two hours at a power level of 50 watts. The temperature of the electrolyte was 28C and the unit was operated in aqueous media at a temperature of 25C, ,...................................................................... :
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Claims (2)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A self-pumping reactive metal anode-aqueous electrolyte electro-chemical cell consisting essentially of a vertical hollow tubular casing, a reactive anode bonded to the interior surface of said casing, said anode naturally forming on its surface a protective insulating film in the presence of water, an expandable coiled metal open-mesh screen cathode positioned within the interior of said tubular casing and contacting said insulating film over substantially all of the anode surface facing said cathode, said cathode pressing continuously against said insulating film during operation of said cell, an aqueous electrolyte filling the interior cavity of said hollow tubular casing and flowing from the bottom to the top of said cell, and a reservoir containing aqueous electrolyte in fluid communication with the top and bottom of said cell, whereby electrolyte is drawn up through said cell by evolved heat and gas generated during operation of said cell and electrolyte is drawn down through said reservoir as it cools.
2. A plurality of electrochemical cells in accordance with claim 1 wherein said cells are connected to a common electrolyte reservoir.
CA232,686A 1974-08-05 1975-08-01 Self-pumping electrochemical cell Expired CA1061856A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US49492974A 1974-08-05 1974-08-05

Publications (1)

Publication Number Publication Date
CA1061856A true CA1061856A (en) 1979-09-04

Family

ID=23966539

Family Applications (1)

Application Number Title Priority Date Filing Date
CA232,686A Expired CA1061856A (en) 1974-08-05 1975-08-01 Self-pumping electrochemical cell

Country Status (6)

Country Link
JP (1) JPS5924503B2 (en)
CA (1) CA1061856A (en)
DE (1) DE2530022C2 (en)
FR (1) FR2281652A1 (en)
GB (1) GB1472516A (en)
IT (1) IT1040459B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3129248A1 (en) * 1981-07-24 1983-02-10 Accumulatorenwerke Hoppecke Carl Zoellner & Sohn GmbH & Co KG, 5790 Brilon GALVANIC ELEMENT, IN PARTICULAR METAL AIR CELL
DE3314174A1 (en) * 1983-04-19 1984-10-25 Volkswagenwerk Ag, 3180 Wolfsburg Arrangement for automatic electrolyte circulation
JPH0592473U (en) * 1992-05-20 1993-12-17 川崎重工業株式会社 Electrical engine cable clamp mechanism for general-purpose engine
WO2002058171A2 (en) * 2001-01-22 2002-07-25 Evionyx, Inc. Electrolyte balance in electrochemical cells
FR3025055B1 (en) * 2014-08-19 2016-08-26 Jomi Leman ELECTROCHEMICAL DEVICE FOR STORING ELECTRIC ENERGY AND HYDROGEN PRODUCTION, AND PROCESS FOR PRODUCING HYDROGEN

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3730776A (en) * 1970-02-04 1973-05-01 Lockheed Aircraft Corp Electric current generator and method using consumable alkali metal anode
US3791871A (en) * 1971-04-14 1974-02-12 Lockheed Aircraft Corp Electrochemical cell

Also Published As

Publication number Publication date
DE2530022C2 (en) 1984-07-12
DE2530022A1 (en) 1976-02-19
FR2281652A1 (en) 1976-03-05
FR2281652B1 (en) 1982-03-05
JPS5924503B2 (en) 1984-06-09
GB1472516A (en) 1977-05-04
JPS5138033A (en) 1976-03-30
IT1040459B (en) 1979-12-20

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